Inpixon Reports 2020 Financial Results and Provides Business Update

Revenues for the Fiscal Year Ended December 31, 2020 Increased 48% Compared to the Same Period Last Year

Conference Call to be Held on March 25th at 4:30 PM Eastern Time

PR Newswire

PALO ALTO, Calif., March 25, 2021 /PRNewswire/ — Inpixon (Nasdaq: INPX), the Indoor Intelligence™ company, today provided a business update and reported financial results for the fiscal year ended December 31, 2020.

Recent Milestones:

  • Secured approximately $78 million in net proceeds through registered direct offerings priced at-the-market, including the exercise of warrants.
  • Partnered with a leading European distributor and integrator of sensors and other electronics to provide Inpixon’s carbon dioxide (CO2) sensor modules for use in measuring indoor air quality–an important indicator of SARS-CoV-2 and other pathogen transmission risk.
  • Launched next-generation chirp RTLS anchor board, Inpixon nanoANQ Chirp PCB, to accelerate the adoption of large-scale, real-time location systems (RTLS) in mass market applications.
  • Announced Inpixon Mapping has been selected as part of a workplace experience solution for a leading medical technology provider, one of the world’s largest public companies, to provide intelligent, multi-layered digital maps.
  • Announced Inpixon Mapping has been selected by one of the world’s premier pharmaceutical companies to provide the visualization required for tracking its critical COVID-19 vaccine-related assets.
  • Completed acquisition of Nanotron Technologies GmbH, a global location awareness technology company.
  • Acquired an exclusive license to market and distribute the SYSTAT and SigmaPlot software suite of data analytics and visualization tools, a transaction accretive to earnings.

Nadir Ali, CEO of Inpixon, commented, “For Inpixon, 2020 was a year of continued growth, expansion and innovation. For the 2020 fiscal year, revenue increased 48% compared to the same period last year. Contributing to our growth, we completed a number of important acquisitions, adding critical technological capabilities, such as on-device positioning, UWB and other RTLS technologies, and expanding our operations in Europe. We have continued to advance our market recognition and industry position among some of the most well recognized brands offering critical capabilities for location-based technologies. We entered 2021 with a strong balance sheet, including approximately $18 million of cash and cash equivalents as of December 31, 2020. We supplemented this by raising an additional $78 million in net proceeds in connection with registered direct offerings, including the exercise of warrants following the end of the period. With our solid financial position, we remain committed to an accelerated growth strategy focused on Indoor Intelligence for people, places and things.

“Based on feedback from customers, the desire for Indoor Intelligence and the adoption of indoor positioning technologies is accelerating and will continue to evolve across a multitude of use cases and industries. As more and more organizations are re-opening and restrictions are being eased to varying degrees, organizations will have to respond to the requirements of a transforming workplace, with concrete measures that support hybrid working models and space rationalization requirements in addition to ensuring the health and safety of employees and visitors. We are at the forefront of delivering a new workplace experience using our mapping and on-device positioning technologies which are essential for providing enterprise-specific solutions with features such as desk booking, cleaning alerts, real-time notifications, and more.

“With our UWB and CSS RTLS tags and anchors, we can offer RTLS technologies that are critical to helping employers keep their workers safe in inherently dangerous environments such as mining and industrial settings. These environments require real-time positioning of people and assets, with positions and distance measurements that need to be calculated in milliseconds in order to support proximity alerts and collision avoidance capabilities for worker safety. We are also innovating by expanding our ability to deliver for these use cases and industries by moving from offering just the chips and modules for RTLS, to delivering complete end user solutions including the related hardware and software, which is expected to increase our average selling price and overall value proposition.

“We are tapping into the growing demand for indoor intelligence and establishing ourselves as an industry leader. We are seeing significant opportunities for continued growth in the workplace experience, industrial environments and other industries that are increasing their reliance on mapping, locationing and analytics technologies to enhance their environments, making them smarter, safer and more secure. We intend to continue to invest in those opportunities. Overall, we remain highly encouraged by the outlook for the business and look forward to accelerating our growth going forward.”

Financial Results

Revenues for the year ended December 31, 2020 were $9.3 million compared to $6.3 million for the comparable period in the prior year for an increase of $3.0 million, or approximately 48%. Revenues increased approximately $1.2 million from the Systat licensing agreement, approximately $0.9 million from the Nanotron acquisition and approximately $0.9 million net increase from existing product lines over the prior comparable period. Gross profit for the year ended December 31, 2020 was $6.7 million compared to $4.7 million for the comparable period in the prior year, an increase of 42%. The gross profit margin for the year ended December 31, 2020 was 72%. Net loss attributable to stockholders for the year ended December 31, 2020 was $29.2 million compared to $34.0 million for the comparable period in the prior year. This decrease in loss of $4.8 million was primarily attributable to the increase in operating expenses offset by the increase in gross margin and the decrease in the valuation allowance adjustment. Non-GAAP Adjusted EBITDA for the year ended December 31, 2020 was a loss of $17.1 million compared to a loss of $11.1 million for the prior year period. EBITDA is defined as net income (loss) before interest, provision for income taxes, and depreciation and amortization. Adjusted EBITDA is used by Inpixon management as a metric by which it manages the business. It is defined as EBITDA plus adjustments for other income or expense items, non-recurring items and other non-cash items including stock-based compensation.

Proforma non-GAAP net loss per basic and diluted common share for the year ended December 31, 2020 was a loss of $0.71 compared to a loss of $18.75 per share for the prior year period. Proforma non-GAAP net income (loss) per share is used by Inpixon management as an evaluation tool as it manages the business and is defined as net income (loss) per basic and diluted share adjusted for non-cash items including stock based compensation, amortization of intangibles and one time charges and other adjustments including provision for valuation allowances, severance costs, provision for doubtful accounts, acquisition costs and costs associated with public offerings.

Conference Call

Inpixon management will host a conference call at 4:30 p.m. Eastern Time on Thursday, March 25, 2021 to discuss the company’s financial results for the fiscal year ended December 31, 2020.

The conference call will be available via telephone by dialing toll free 888-506-0062 for U.S. callers or +1 973-528-0011 for international callers and using entry code 549014. A webcast of the call may be accessed at https://www.webcaster4.com/Webcast/Page/2235/40338 or on the company’s Investor Relations section of the website, ir.inpixon.com.

Investors and other interested parties are invited to submit questions to management prior to the call’s start via email to [email protected].

A webcast replay will be available on the company’s Investor Relations section of the website (ir.inpixon.com) through March 25, 2022. A telephone replay of the call will be available approximately one hour following the call, through April 1, 2021 and can be accessed by dialing 877-481-4010 for U.S. callers or +1 919-882-2331 for international callers and entering conference ID 40338.

About Inpixon

Inpixon® (Nasdaq: INPX) is the Indoor Intelligence™ company that specializes in capturing, interpreting and giving context to indoor data so it can be translated into actionable intelligence. The company’s Indoor Intelligence platform ingests diverse data from IoT, third-party and proprietary sensors designed to detect and position active cellular, Wi-Fi, UWB and Bluetooth devices. Paired with a high-performance data analytics engine, patented algorithms, and advanced mapping technology, Inpixon’s solutions are leveraged by a multitude of industries to do good with indoor data. This multidisciplinary depiction of indoor data enables users to increase revenue, decrease costs, and enhance safety. Inpixon customers can boldly take advantage of location awareness, analytics, sensor fusion and the Internet of Things (IoT) to uncover the untold stories of the indoors. For the latest insights, follow Inpixon on LinkedInTwitter, and visit inpixon.com.

Safe Harbor Statement

All statements in this release that are not based on historical fact are “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995 and the provisions of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. While management has based any forward-looking statements included in this release on its current expectations, the information on which such expectations were based may change. These forward-looking statements rely on a number of assumptions concerning future events and are subject to a number of risks, uncertainties and other factors, many of which are outside of the control of Inpixon and its subsidiaries, which could cause actual results to materially differ from such statements. Such risks, uncertainties, and other factors include, but are not limited to, the fluctuation of economic conditions, the impact of COVID-19 on Inpixon’s results of operations, Inpixon’s ability to integrate the products and business from recent acquisitions into its existing business, the performance of management and employees, the regulatory landscape as it relates to privacy regulations and their applicability to Inpixon’s technology, Inpixon’s ability to maintain compliance with Nasdaq’s minimum bid price requirement and other continued listing requirements, the ability to obtain financing, competition, general economic conditions and other factors that are detailed in Inpixon’s periodic and current reports available for review at sec.gov. Furthermore, Inpixon operates in a highly competitive and rapidly changing environment where new and unanticipated risks may arise. Accordingly, investors should not place any reliance on forward-looking statements as a prediction of actual results. Inpixon disclaims any intention to, and undertakes no obligation to, update or revise forward-looking statements.

Non-GAAP Financial Measures

Management believes that certain financial measures not in accordance with generally accepted accounting principles in the United States (“GAAP”) are useful measures of operations. EBITDA, Adjusted EBITDA and pro forma net loss per share are non-GAAP measures. Inpixon defines “EBITDA” as net income (loss) before interest, provision for (benefit from) income taxes, and depreciation and amortization. Management uses Adjusted EBITDA as the matrix in which it manages the business and Inpixon defines “Adjusted EBITDA” as EBITDA plus adjustments for deemed dividends, other income or expense items, non-recurring items and non-cash items. Inpixon defines “pro forma net loss per share” as GAAP net loss per share adjusted for non-cash items including stock based compensation, amortization of intangibles and one time charges and other adjustments including provision for valuation allowances, severance costs, provision for doubtful accounts,  acquisition costs and costs associated with public offerings.

Management provides Adjusted EBITDA and pro forma net loss per share measures so that investors will have the same financial information that management uses, which may assist investors in assessing Inpixon’s performance on a period-over-period basis. Adjusted EBITDA or pro forma net loss per share is not a measure of financial performance under GAAP, and should not be considered an alternative to net income (loss) or any other measure of performance under GAAP, or to cash flows from operating, investing or financing activities as an indicator of cash flows or as a measure of liquidity. Adjusted EBITDA and pro forma net loss per share have limitations as analytical tools and should not be considered either in isolation or as a substitute for analysis of Inpixon’s results as reported under GAAP.  For more information on our non-GAAP financial measures and a reconciliation of GAAP to non-GAAP measures, please see the “Reconciliation of Non-GAAP Financial Measures” table accompanying this press release.

Inpixon Contacts

Media relations and general inquiries:

Inpixon
Email: [email protected]
Web: inpixon.com/contact-us

Investor relations:

Crescendo Communications, LLC
Tel: +1 212-671-1020
Email: [email protected]

 


INPIXON AND SUBSIDIARIES


 CONDENSED CONSOLIDATED BALANCE SHEETS


(In thousands, except number of shares and par value data)

As of

December 31, 2020

December 31, 2019


ASSETS


Current Assets

Cash and cash equivalents

$

17,996

$

4,777

Accounts receivable, net

1,739

1,108

Notes and other receivables

152

74

Inventory

1,243

400

Short-term investments

7,998

0

Prepaid assets and other current assets

1,197

406


Total Current Assets

30,325

6,765

Property and equipment, net

1,445

145

Operating lease right-of-use asset, net

2,077

1,585

Software development costs, net

1,721

1,544

Long-term investments

2,500

0

Intangible assets, net

14,203

8,400

Goodwill

6,588

2,070

Receivable from related party

616

Other assets

152

94


Total Assets

$

59,011

$

21,219


LIABILITIES AND STOCKHOLDERS’ EQUITY


Current Liabilities

Accounts payable

$

908

$

2,383

Accrued liabilities

2,739

1,863

Operating lease obligation, current

647

776

Deferred revenue

1,922

912

Short-term debt

5,401

7,304

Acquisition liability

500

502


Total Current Liabilities

12,117

13,740


Long Term Liabilities

Operating lease obligations, noncurrent

1,457

837

Other liabilities, noncurrent

7

7

Deferred tax liability, noncurrent

87

Acquisition liability, noncurrent

750

500


Total Liabilities

14,331

15,171


Commitments and Contingencies


Stockholders’ Equity

Preferred Stock – $0.001 par value; 5,000,000 shares authorized, consisting of Series 4 ConvertiblePreferred Stock – 10,415
shares authorized; 1 and 1 issued, and 1 and 1 outstanding as of December 31, 2020 and 2019, respectively, Series 5 Convertible
Preferred Stock – 12,000 shares authorized; 126 and 126 issued, and 126 and 126 outstanding as of December 31,2020 and 2019,
respectively.

Common Stock – $0.001 par value; 250,000,000 shares authorized; 53,178,462 and 4,234,923 issued and 53,178,461 and 
4,234,922 outstanding as of December 31, 2020 and 2019, respectively.

53

4

Additional paid-in capital

225,613

158,382

Treasury stock, at cost, 1 share

(695)

(695)

Accumulated other comprehensive income

660

94

Accumulated deficit (excluding $2,442 reclassified to additional paid in capital in quasi-reorganization)

(180,992)

(151,763)

Stockholders’ Equity Attributable to Inpixon

44,639

6,022

Non-controlling interest

41

26


Total Stockholders’ Equity

44,680

6,048


Total Liabilities and Stockholders’ Equity

$

59,011

$

21,219

 


INPIXON AND SUBSIDIARIES


 CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS


(In thousands, except per share data)

For the Years Ended

December 31,

2020

2019


Revenues

$

9,297

$

6,301


Cost of Revenues

2,613

1,609


Gross Profit

6,684

4,692


Operating Expenses

Research and development

6,523

3,893

Sales and marketing

5,331

3,043

General and administrative

15,261

13,660

Acquisition related costs

1,057

1,277

Amortization of intangibles

2,306

3,629


Total Operating Expenses

30,478

25,502


Loss from Operations

(23,794)

(20,810)


Other Income (Expense)

Interest expense, net

(2,426)

(2,277)

Loss on exchange of debt for equity

(210)

(294)

Provision for valuation allowance on held for sale loan

(2,370)

(10,627)

Other income (expense)

(470)

(558)


Total Other Income (Expense)

(5,476)

(13,756)


Net Loss, before tax

(29,270)

(34,566)

Income tax benefit

56

584


Net Loss

(29,214)

(33,982)


Net Income Attributable to Non-controlling Interest

15

9


Net Loss Attributable to Stockholders of Inpixon

$

(29,229)

$

(33,991)

Deemed dividend for triggering of warrant down round feature

(1,250)


Net Loss Attributable to Common Stockholders

$

(29,229)

$

(35,241)


Net Loss Per Share – Basic and Diluted

$

(1.01)

$

(47.52)


Weighted Average Shares Outstanding

Basic and Diluted

28,800,493

741,530


Comprehensive Loss

Net Loss

$

(29,214)

$

(33,982)

Unrealized foreign exchange gain/(loss) from cumulative translation adjustments

566

68


Comprehensive Loss

$

(28,648)

$

(33,914)

 


INPIXON AND SUBSIDIARIES


CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS


(In thousands)

For the Years Ended

December 31,

2020

2019


Cash Flows Used In Operating Activities

  Net loss

$

(29,214)

$

(33,982)

Adjustments to reconcile net loss to net cash used in operating activities:

Depreciation and amortization

826

1,123

Amortization of intangible assets

2,545

3,633

Amortization of right of use asset

490

398

Stock based compensation

1,194

3,489

Amortization of technology

66

Loss on exchange of debt for equity

210

294

Amortization of debt discount

2,594

2,221

Accrued interest income, related party

(32)

Provision for doubtful accounts

956

558

Provision for inventory obsolescence

138

Provision for the valuation allowance held for sale loan

2,370

10,627

Provision for the valuation allowance related party receivable

648

Income tax benefit

(87)

(584)

Other

(6)

(223)

Changes in operating assets and liabilities:

Accounts receivable and other receivables

(964)

46

Inventory

(117)

171

Other current assets

(563)

156

Other assets

(248)

(412)

Accounts payable

(1,815)

1,189

Accrued liabilities

269

521

Deferred revenue

242

(507)

Operating lease liabilities

(490)

Other liabilities

453

551

Total Adjustments

8,613

23,317


Net Cash Used in Operating Activities

(20,601)

(10,665)


Cash Flows Used in Investing Activities

   Purchase of property and equipment

(972)

(89)

Investment in capitalized software

(862)

(927)

Investment in short term investment

(7,998)

Cash paid for the Systat Licensing Agreement

(2,200)

Cash paid for the acquisition of Ten Degrees

(1,500)

Cash paid for the acquisition of Nanotron

(7,786)

Investment in long term investment

(2,500)

Cash paid for the acquisition of GTX

(250)

Cash paid for the acquisition of Locality

(204)

Cash paid for the acquisition of Jibestream

(3,714)

Cash acquired in the Locality acquisition

70

Cash acquired in the Jibestream acquisition

6

Cash acquired in the Nanotron acquisition

311


Net Cash Flows Used in Investing Activities

(23,507)

(5,108)


Cash Flows From Financing Activities

Net (repayments) proceeds to bank facility

(150)

127

Net proceeds from issuance of common stock, preferred stock and warrants

55,352

20,725

Net repayments of notes payable

(74)

(70)

Loans to related party

(2,569)

(10,276)

Repayments from related party

200

1,832

Advances to related party

(31)

Loan to Jibestream

(141)

Loan to GTX

(50)

Net proceeds from promissory notes

5,000

7,500

Repayment of acquisition liability to Locality shareholders

(500)

(210)


Net Cash Provided By Financing Activities

57,259

19,406


Effect of Foreign Exchange Rate on Changes on Cash

(4)

68


Net (Decrease) Increase in Cash, Cash Equivalents and Restricted Cash

13,147

3,701

Cash, Cash Equivalents and Restricted Cash – Beginning of period

4,849

1,148

Cash, Cash Equivalents and Restricted Cash – End of period

$

17,996

$

4,849

 


Reconciliation of Non-GAAP Financial Measures:

(In thousands)


For the Years Ended


December 31,


2020


2019

Net loss attributable to common stockholders

$

(29,229)

$

(35,241)

Adjustments:

Non-recurring one-time charges:

Loss on exchange of debt for equity

210

294

Provision for valuation allowance on held for sale loan

2,370

10,627

Provision for the valuation allowance related party receivable

648

Settlement of litigation

6

Acquisition transaction/financing costs

1,057

1,277

Costs associated with public offering

50

Severance

161

Bad debts expense/provision

956

558

Deemed dividend for triggering of warrant down round feature

1,250

Stock-based compensation – compensation and related benefits

1,194

3,489

Interest expense, net

2,426

2,277

Income tax benefit

(87)

(584)

Depreciation and amortization

3,371

4,752

Adjusted EBITDA

$

(17,084)

$

(11,084)

(In thousands, except share data)


For the Years Ended


December 31,


2020


2019

Net loss attributable to common stockholders

$

(29,229)

$

(35,241)

Adjustments:

Non-recurring one-time charges:

Loss on exchange of debt for equity

210

294

Provision for valuation allowance on held for sale loan

2,370

10,627

Provision for the valuation allowance related party receivable

648

Settlement of litigation

6

Acquisition transaction/financing costs

1,057

1,277

Costs associated with public offering

50

Severance

161

Bad debts expense/provision

956

558

Deemed dividend for triggering of warrant down round feature

1,250

Stock-based compensation – compensation and related benefits

1,194

3,489

Amortization of intangibles

2,306

3,629

Proforma non-GAAP net loss

$       (20,488)

$    (13,900)

Proforma non-GAAP net loss per basic and diluted common share

$           (0.71)

$

(18.75)

Weighted average basic and diluted common shares outstanding

28,800,493

741,530

 

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SOURCE Inpixon

G Squared Ascend I Inc. Securities to commence separate trading

PR Newswire

CHICAGO, March 25, 2021 /PRNewswire/ — G Squared Ascend I Inc. (NYSE: GSQD.U) (the “Company”) announced today that separate trading of its common stock and warrants underlying the Company’s units would commence on or about March 26, 2021. The common stock and warrants will trade under the symbols “GSQD” and “GSQD.W”, respectively. Units not separated will continue to be listed on the New York Stock Exchange under the symbol “GSQD.U”.

G Squared Ascend I Inc. is a newly incorporated blank check company, incorporated as a Cayman Islands exempted company for the purpose of effecting a merger, share exchange, asset acquisition, share purchase, reorganization or similar business combination with one or more businesses or entities, which we refer to as our initial business combination. While G Squared Ascend I Inc. may pursue an initial business combination opportunity in any business, industry, sector or geographical location, it intends to focus its search within the technology sector, and specifically within six core verticals or “megatrends,” including: Software-as-a-Service, Online Marketplaces, Mobility 2.0/Logistics, Fintech/Insurtech, New Age Media and Sustainability.

This press release shall not constitute an offer to sell or a solicitation of an offer to buy, nor shall there be any sale of these securities in any state or jurisdiction in which such offer, solicitation or sale would be unlawful prior to registration or qualification under the securities laws of any such state or jurisdiction.

Forward Looking Statements

This press release contains statements that constitute “forward-looking statements” within the meaning of the federal securities laws. Forward-looking statements are subject to numerous risks and conditions, many of which are beyond the control of the Company, including those set forth in the Risk Factors section of the Company’s registration statement and other filings with the Securities and Exchange Commission and, therefore, actual results could differ materially from those projected in the forward-looking statements. The Company undertakes no obligation to update these statements for revisions or changes after the date of this release, except as required by law.

Contacts:

Antonia Korduba

[email protected]

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SOURCE G Squared Ascend I Inc.

Oxford: Owner of Tommy Bahama, Lilly Pulitzer, and Southern Tide Reports Fourth Quarter and Full Fiscal Year 2020 Results

–Continued Strength in E-commerce–

–Provides Guidance for First Quarter and Fiscal 2021–

–Restores Dividend to pre-COVID level of $0.37 per Share; a 48% Increase Compared to Prior Dividend–

ATLANTA, March 25, 2021 (GLOBE NEWSWIRE) — Oxford Industries, Inc. (NYSE: OXM) today announced financial results for its fourth quarter and fiscal 2020 year ended January 30, 2021.   Consolidated net sales were $221 million in the fourth quarter of fiscal 2020 compared to $298 million in the fourth quarter of fiscal 2019. On a GAAP basis, the Company reported a loss of $0.74 per share in the fourth quarter of fiscal 2020 as compared to earnings of $0.90 per share in the same period of the prior year. Adjusted earnings were $0.13 per share in the fourth quarter of fiscal 2020 compared to adjusted earnings of $1.09 per share in the fourth quarter of fiscal 2019.

Full fiscal year consolidated net sales were $749 million in fiscal 2020 compared to $1.123 billion in fiscal 2019. The Company reported a loss of $5.77 per share on a GAAP basis in fiscal 2020 compared to earnings of $4.05 per share in fiscal 2019. On an adjusted basis, the Company reported a loss of $1.81 per share compared to earnings of $4.32 per share in fiscal 2019.  

The Company’s adjusted results in the fourth quarter of fiscal 2020 exclude a $15 million asset write-off related to an information technology project, and $3 million of charges related to the exit of Lanier Apparel. The Company’s full year adjusted results exclude a $60 million Southern Tide impairment charge, the $15 million technology project write-off and $13 million of charges related to the exit of Lanier Apparel, partially offset by a $9 million favorable impact of LIFO accounting. More details can be found in the reconciliation table at the end of this release.

The Company finished fiscal 2020 in a strong liquidity position with $66 million of cash and cash equivalents and no borrowings outstanding under its revolving credit agreement. Unused availability was $301 million at the end of fiscal 2020. The Company finished fiscal 2019 with $52 million of cash and cash equivalents and no borrowings outstanding. The improvement in the Company’s liquidity position was attributable to $84 million of cash flow from operations which funded capital expenditures, share repurchases, dividends and minority investments in smaller branded businesses.

Thomas C. Chubb III, Chairman and Chief Executive Officer, commented, ”This time last year, we were facing incredible uncertainties related to the pandemic, its duration and its effect on our business. In response we established three priorities for fiscal 2020: protect our people and our customers, protect our brands, and preserve liquidity. We were successful in achieving these important and fundamental goals. At the same time, as we moved through the year and our business gained momentum, it became even more evident that the strong strategic positioning of our brands in the marketplace combined with our omni-channel capabilities provides us with clear and compelling competitive advantages. The key learnings from the past year have helped further sharpen our focus on our highest return opportunities.”

“It is clear that e-commerce will be bigger and more important than ever following the accelerated shift to online spending during the pandemic,” continued Mr. Chubb. “The strength of our e-commerce platforms and our digital outreach to consumers led to a 28% increase in our full price e-commerce businesses in fiscal 2020. We added to these capabilities in 2020 and expanding our expertise and investment in digital will remain a priority in 2021 and beyond.”

“Despite the significant impact of temporary store closures and operating restrictions in 2020, we are confident that our retail strategy is going to serve us well as conditions normalize. Our 187 full-price retail stores are in desirable locations, where shopping is still entertainment. We believe food and beverage is an important complement to our beautiful stores and will continue to play a larger role in our retail evolution. In 2020, we opened four additional Tommy Bahama Marlin Bars and we will continue to invest in this promising concept moving forward. Whether online or in our stores and restaurants, we are committed to enhancing and delivering a shopping experience that recognizes and serves the customer in their brand discovery and purchasing preferences now and in the future.”

Mr. Chubb concluded, “Each of our brands – Tommy Bahama, Lilly Pulitzer, Southern Tide, The Beaufort Bonnet Company and Duck Head, simply put, make people happy. Our talented, highly engaged teams will continue to evolve and update our products and brand messaging to ensure they stay relevant for today’s consumer and remain true to each brand’s unique DNA. This has been and will continue to be the key to our success as we deliver long-term value to our shareholders.”

Summary of Results

  • Consolidated net sales decreased 26% in the fourth quarter of fiscal 2020 compared to the fourth quarter last year. For the full 2020 fiscal year, consolidated net sales decreased 33%.
    • Full price e-commerce sales grew 26% and 28% in the fourth quarter and the full year, respectively, with growth in all the Company’s branded businesses in the year.
    • The Company, which temporarily closed its retail stores and restaurants in March 2020, began a gradual reopening of locations in the second quarter. At the time of this release, substantially all stores and restaurants are open, but many continue to operate under varying degrees of restricted conditions for the safety of employees and customers.
      • Full price retail sales were 43% and 56% lower, respectively, in the fourth quarter and full year.
      • Restaurant sales were 29% and 42% lower, respectively, in the fourth quarter and full year.
    • Wholesale sales decreased 48% in the fourth quarter and the full year.
  • Gross margin was 54.3% in the fourth quarter compared to 55.9% in the fourth quarter last year. For the full year gross margin was 55.4% compared to 57.4% in fiscal 2019, with gross margin lower in each operating group. Gross margin was negatively impacted by a more promotional environment due to COVID-19 and inventory markdown charges, which were partially offset by LIFO accounting credits.
  • SG&A decreased 6% or $8 million in the fourth quarter and 13% or $74 million in the full year on a GAAP basis. On an adjusted basis, SG&A decreased 17% or $24 million in the fourth quarter and 17% or $93 million in the full year. Cost savings measures in fiscal 2020 included a $63 million reduction in employment costs, a $10 million reduction in occupancy costs, and reductions in variable and other expenses.
  • In the fourth quarter, the Company reported an operating loss of $17 million compared to an operating profit of $21 million in the same period of the prior year. On an adjusted basis, operating income was $3 million compared to $25 million in the fourth quarter of fiscal 2019. For the full 2020 fiscal year, the Company reported an operating loss of $124 million compared to an operating profit of $94 million in fiscal 2019. For the full year, on an adjusted basis, the Company’s operating loss was $43 million in fiscal 2020 compared to an operating profit of $99 million in the prior year.
  • The effective tax rate in the fourth quarter was a benefit of 28% compared to a charge of 27% in the fourth quarter of fiscal 2019. For the full year, the effective tax rate was a benefit of 24% compared to a charge of 26% in the prior year.
  • The Company reported a loss per share of $0.74 on a GAAP basis and income per share of $0.13 on an adjusted basis in the fourth quarter of fiscal 2020. For the full year, the Company reported a loss of $5.77 on a GAAP basis and $1.81 on an adjusted basis.

Balance Sheet and Liquidity

Inventory decreased 19% to $124 million at the end of the fourth quarter compared to $152 million in the prior year with double-digit percentage decreases in each operating group.

As of January 30,  2021, the Company had a strong liquidity position with $66 million of cash and cash equivalents and no borrowings outstanding under its revolving credit agreement. Unused availability was $301 million at the end of fiscal 2020.   At the end of the prior year, the Company had $52 million of cash and cash equivalents and no borrowings outstanding.

The Company believes its strong liquidity position will satisfy ongoing cash requirements for the foreseeable future. These cash requirements generally consist of working capital and other operating activity needs, capital expenditures and dividend payments.

In the full 2020 fiscal year, cash provided by operating activities was $84 million, which funded $29 million of capital expenditures, primarily for information technology initiatives to enhance our capabilities with regard to data, digital marketing and omni-channel retail, as well as investments in Marlin Bars and retail stores, resulting in free cash flow of $55 million. In fiscal 2020, the Company also paid dividends of $17 million, repurchased $20 million of shares and invested $6 million for minority interests in smaller branded apparel businesses.

Dividend

The Board of Directors declared a quarterly cash dividend of $0.37 per share, a 48% increase from the previous level of $0.25 per share. The dividend is payable on April 30, 2021 to shareholders of record as of the close of business on April 16, 2021. The Company has paid dividends every quarter since it became publicly owned in 1960.

Fiscal 2021 Outlook

For the full 2021 fiscal year, ending on January 29, 2022, the Company expects net sales to grow to between $940 million and $980 million as compared to net sales of $749 million in fiscal 2020. In fiscal 2021, GAAP earnings per share are expected to be between $2.65 and $3.05. Adjusted earnings per share are expected to be between $2.80 and $3.20. This compares to a loss on a GAAP basis of $5.77 per share and an adjusted loss of $1.81 per share in fiscal 2020.

For the first quarter of fiscal 2021, ending May 1, 2021, the Company expects net sales in a range of $220 million to $240 million, as compared to $160 million in the first quarter of fiscal 2020. In the first quarter of fiscal 2021, GAAP earnings per share are expected to be between $0.90 and $1.10. Adjusted earnings per share are expected to be between $0.95 and $1.15. This compares to a loss on a GAAP basis of $4.02 per share and an adjusted loss of $1.12 per share in the first quarter of fiscal 2020.  

The Company’s interest expense is expected to be approximately $1 million. The Company’s effective tax rate for the first quarter is expected to be approximately 15% and for fiscal 2021 is expected to be approximately 20%. The tax rate for both the quarter and year are expected to benefit from certain discrete items.

Capital expenditures in fiscal 2021 are expected to be approximately $35 million, compared to $29 million in fiscal 2020, primarily reflecting investments in information technology initiatives and new Marlin Bars.

Conference Call

The Company will hold a conference call with senior management to discuss its financial results at 4:30 p.m. ET today. A live web cast of the conference call will be available on the Company’s website at www.oxfordinc.com. A replay of the webcast will be available on the Company’s website through April 8, 2021 or by dialing (412) 317-6671 access code 13717600.

About Oxford

Oxford Industries, Inc., a leader in the apparel industry, owns and markets the distinctive Tommy Bahama®, Lilly Pulitzer® and Southern Tide® lifestyle brands, as well as other owned brands. Oxford’s stock has traded on the New York Stock Exchange since 1964 under the symbol OXM. For more information, please visit Oxford’s website at www.oxfordinc.com.

Basis of Presentation

All per share information is presented on a diluted basis.

Non-GAAP Financial Information

The Company reports its consolidated financial statements in accordance with generally accepted accounting principles (GAAP).  To supplement these consolidated financial results, management believes that a presentation and discussion of certain financial measures on an adjusted basis, which exclude certain non-operating or discrete gains, charges or other items, may provide a more meaningful basis on which investors may compare the Company’s ongoing results of operations between periods.  These measures include adjusted earnings, adjusted earnings per share, adjusted gross profit, adjusted gross margin, adjusted SG&A, and adjusted operating income, among others.

Management uses these non-GAAP financial measures in making financial, operational, and planning decisions to evaluate the Company’s ongoing performance. Management also uses these adjusted financial measures to discuss its business with investment and other financial institutions, its board of directors and others.  Reconciliations of these adjusted measures to the most directly comparable financial measures calculated in accordance with GAAP are presented in tables included at the end of this release.

Safe Harbor

This press release includes statements that constitute forward-looking statements within the meaning of the federal securities laws. Generally, the words “believe,” “expect,” “intend,” “estimate,” “anticipate,” “project,” “will” and similar expressions identify forward-looking statements, which typically are not historical in nature. We intend for all forward-looking statements contained herein, in our press releases or on our website, and all subsequent written and oral forward-looking statements attributable to us or persons acting on our behalf, to be covered by the safe harbor provisions for forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 and the provisions of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934 (which Sections were adopted as part of the Private Securities Litigation Reform Act of 1995). Such statements are subject to a number of risks, uncertainties and assumptions including, without limitation, the impact of the ongoing coronavirus (COVID-19) pandemic, including uncertainties about its scope and duration (including resurgence of COVID-19 cases), future store closures or other restrictions (including reduced hours and capacity) due to government mandates, and the effectiveness of store re-openings and reduction initiatives (including our ability to effectively renegotiate rent obligations), any or all of which may also affect many of the following risks; demand for our products, which may be impacted by competitive conditions and/or evolving consumer shopping patterns; macroeconomic factors that may impact consumer discretionary spending for apparel and related products; the impact of any restructuring initiatives we may undertake in one or more of our business lines, including the process, timing, costs, uncertainties and effects of our announced exit of the Lanier Apparel business; costs of products as well as the raw materials used in those products; expected pricing levels; costs of labor; the timing of shipments requested by our wholesale customers; expected outcomes of pending or potential litigation and regulatory actions; changes in international, federal or state tax, trade and other laws and regulations, including the potential imposition of additional duties; the ability of business partners, including suppliers, vendors, licensees and landlords, to meet their obligations to us and/or continue our business relationship to the same degree in light of current or future financial stress, staffing shortages, liquidity challenges and/or bankruptcy filings; weather; fluctuations and volatility in global financial markets; retention of and disciplined execution by key management; the timing and cost of store and restaurant openings and remodels, technology implementations and other capital expenditures; acquisition and disposition activities, including our ability to timely recognize expected synergies from acquisitions; access to capital and/or credit markets; the impact of tax and other legislative changes; changes in accounting standards and related guidance; and factors that could affect our consolidated effective tax rate, including estimated Fiscal 2020 taxable losses eligible for carry back under the CARES Act. Forward-looking statements reflect our expectations at the time such forward-looking statements are made, based on information available at such time, and are not guarantees of performance. Although we believe that the expectations reflected in such forward-looking statements are reasonable, these expectations could prove inaccurate as such statements involve risks and uncertainties, many of which are beyond our ability to control or predict. Should one or more of these risks or uncertainties, or other risks or uncertainties not currently known to us or that we currently deem to be immaterial, materialize, or should underlying assumptions prove incorrect, actual results may vary materially from those anticipated, estimated or projected. Important factors relating to these risks and uncertainties include, but are not limited to, those described in Part I, Item 1A. contained in our Annual Report on Form 10-K for the period ended February 1, 2020 under the heading “Risk Factors” and those described from time to time in our subsequent and future reports filed with the SEC, including our Quarterly Reports on Form 10-Q for the fiscal quarters ended May 2, 2020 and October 31, 2020. You should not place undue reliance on forward-looking statements, which speak only as of the date on which they are made.  We disclaim any intention, obligation, or duty to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise, except as required by law.

Contact:    Anne M. Shoemaker
E-mail:   [email protected]

                                                                                           

Oxford Industries, Inc.
Consolidated Balance Sheets
(in thousands, except par amounts)
(unaudited)
     January 30,   February 1,
    2021


  2020


ASSETS            
Current Assets            
Cash and cash equivalents   $        
66,013
    $ 52,460  
Receivables, net            
30,418
      57,862  
Inventories, net         
123,543
      152,229  
Income tax receivable            
17,975
      862  
Prepaid expenses and other current assets            
20,367
      25,413  
Total Current Assets   $     
258,316
    $ 288,826  
Property and equipment, net         
159,732
      191,517  
Intangible assets, net         
156,187
      175,005  
Goodwill            
23,910
      66,578  
Operating lease assets         
233,775
      287,181  
Other assets, net            
33,714
      24,262  
Total Assets   $     
865,634
    $ 1,033,369  
             
LIABILITIES AND SHAREHOLDERS’ EQUITY      
  
 
     
Current Liabilities            
Accounts payable   $        
71,148
    $ 65,491  
Accrued compensation            
18,897
      19,363  
Current portion of operating lease liabilities            
60,886
      50,198  
Accrued expenses and other liabilities            
45,321
      42,727  
Total Current Liabilities   $     
196,252
    $ 177,779  
Long-term debt                    
       
Non-current portion of operating lease liabilities         
239,963
      291,886  
Other non-current liabilities            
23,691
      18,566  
Deferred income taxes                    
      16,540  
Shareholders’ Equity            
Common stock, $1.00 par value per share            
16,889
      17,040  
Additional paid-in capital         
156,508
      149,426  
Retained earnings         
235,995
      366,793  
Accumulated other comprehensive loss            
(3,664
)     (4,661 )
Total Shareholders’ Equity         
405,728
      528,598  
Total Liabilities and Shareholders’ Equity   $     
865,634
    $ 1,033,369  

 

Oxford Industries, Inc.
Consolidated Statements of Operations
(in thousands, except per share amounts)
(unaudited)
    Fourth Quarter   Full Year
    Fiscal 2020   Fiscal 2019   Fiscal 2020   Fiscal 2019
Net sales   $ 221,367     $ 297,596     $ 748,833     $ 1,122,790  
Cost of goods sold     101,240       131,203       333,626       477,823  
Gross profit   $ 120,127     $ 166,393     $ 415,207     $ 644,967  
SG&A     140,427       148,701       492,628       566,149  
Impairment of goodwill and intangible assets                 60,452        
Royalties and other operating income     3,675       3,388       14,024       14,857  
Operating (loss) income   $ (16,625 )   $ 21,080     $ (123,849 )   $ 93,675  
Interest expense, net     355       74       2,028       1,245  
(Loss) earnings before income taxes   $ (16,980 )   $ 21,006     $ (125,877 )   $ 92,430  
Income tax (benefit) provision     (4,763 )     5,674       (30,185 )     23,937  
Net (loss) earnings   $ (12,217 )   $ 15,332     $ (95,692 )   $ 68,493  
                             
Net (loss) earnings per share:                    
  
 
       
Basic   $ (0.74 )   $ 0.91     $ (5.77 )   $ 4.09  
Diluted   $ (0.74 )   $ 0.90     $ (5.77 )   $ 4.05  
Weighted average shares outstanding:                    
  
 
       
Basic     16,577       16,779       16,576       16,756  
Diluted     16,577       16,965       16,576       16,914  
Dividends declared per share   $ 0.25     $ 0.37     $ 1.00     $ 1.48  

 

Oxford Industries, Inc.
Consolidated Statements of Cash Flows
(in thousands)
(unaudited)
    Full Year
    Fiscal 2020      Fiscal 2019
Cash Flows From Operating Activities:            
Net (loss) earnings   $        
(95,692
)   $ 68,493  
Adjustments to reconcile net earnings (loss) to cash flows from operating activities:            
Depreciation             
38,975
      38,026  
Amortization of intangible assets                
1,111
      1,171  
Impairment of goodwill and intangible assets             
60,452
       
Impairment of property and equipment             
19,828
      1,090  
Equity compensation expense                
7,755
      7,620  
Amortization of deferred financing costs                   
344
      384  
Change in fair value of contingent consideration                   
593
      431  
Deferred income taxes (benefit) expense            
(18,332
)     (1,973 )
Changes in operating assets and liabilities, net of acquisitions and dispositions:      
  
 
     
Receivables, net             
28,429
      10,252  
Inventories, net             
29,355
      8,187  
Income tax receivable            
(17,113
)     19  
Prepaid expenses and other current assets                
5,064
      606  
Current liabilities             
17,611
      (14,282 )
Other non-current assets, net             
53,819
      (283,335 )
Other non-current liabilities            
(48,349
)     285,237  
Cash provided by operating activities   $         
83,850
    $ 121,926  
Purchases of property and equipment            
(28,924
)     (37,421 )
Other investing activities              
(5,727
)      
Cash used in investing activities   $        
(34,651
)   $ (37,421 )
Cash Flows From Financing Activities:            
Repayment of revolving credit arrangements         
(280,963
)     (122,241 )
Proceeds from revolving credit arrangements           
280,963
      109,248  
Deferred financing costs paid                      
      (952 )
Repurchase of common stock            
(18,053
)      
Proceeds from issuance of common stock                
1,378
      1,639  
Repurchase of equity awards for employee tax withholding liabilities              
(1,870
)     (2,728 )
Cash dividends declared and paid            
(16,844
)     (25,215 )
Other financing activities                 
(459
)     (1,049 )
Cash used in financing activities   $        
(35,848
)   $ (41,298 )
Net change in cash and cash equivalents   $         
13,351
    $ 43,207  
Effect of foreign currency translation on cash and cash equivalents                   
202
      926  
Cash and cash equivalents at the beginning of year             
52,460
      8,327  
Cash and cash equivalents at the end of year   $         
66,013
    $ 52,460  

 

Oxford Industries, Inc.
Reconciliations of Certain Non-GAAP Financial Information
(in millions, except per share amounts)
(unaudited)
     Fourth Quarter
     Full Year
 
AS REPORTED    
Fiscal 2020


   
Fiscal 2019


% Change    Fiscal 2020
   Fiscal 2019
% Change
Tommy Bahama                            
Net sales   $ 142.7     $ 196.0   (27.2 )%   $ 419.8     $ 676.7   (38.0 )%
Gross profit   $ 82.5     $ 118.7   (30.5 )%   $ 244.2     $ 413.2   (40.9 )%
Gross margin     57.8 %     60.6 %       58.2 %     61.1 %  
Operating (loss) income   $ (10.0 )   $ 22.5   NM   $ (53.3 )   $ 53.2   NM
Operating margin     (7.0 )%     11.5 %       (12.7 )%     7.9 %  
Lilly Pulitzer                            
Net sales   $ 54.4     $ 64.9   (16.2 )%   $ 231.1     $ 284.7   (18.8 )%
Gross profit   $ 29.4     $ 36.3   (19.1 )%   $ 138.0     $ 174.6   (21.0 )%
Gross margin     54.1 %     56.0 %       59.7 %     61.3 %  
Operating income   $ 2.0     $ 5.1   (60.4 )%   $ 27.7     $ 51.8   (46.5 )%
Operating margin     3.7 %     7.9 %       12.0 %     18.2 %  
Southern Tide                            
Net sales   $ 7.5     $ 10.7   (29.7 )%   $ 34.7     $ 46.4   (25.3 )%
Gross profit   $ 3.9     $ 5.1   (24.0 )%   $ 11.8     $ 22.8   (48.2 )%
Gross margin     51.5 %     47.6 %       34.1 %     49.1 %  
Operating income (loss)   $ 0.0     $ 0.7   (98.8 )%   $ (64.8 )   $ 5.6   NM
Operating margin     0.1 %     6.4 %       (186.9 )%     12.0 %  
Lanier Apparel

(1)
                           
Net sales   $ 8.8     $ 19.8   (55.5 )%   $ 38.8     $ 95.2   (59.2 )%
Gross profit   $ 0.9     $ 3.9   (77.1 )%   $ 0.3     $ 25.1   (98.8 )%
Gross margin     10.1 %     19.5 %       0.8 %     26.4 %  
Operating (loss) income   $ (5.4 )   $ (1.8 ) (201.6 )%   $ (26.7 )   $ 2.0   NM
Operating margin     (61.1 )%     (9.0 )%       (68.7 )%     2.1 %  
Corporate and Other

(1)
                           
Net sales   $ 8.0     $ 6.1   30.1 %   $ 24.5     $ 19.8   23.4 %
Gross profit   $ 3.5     $ 2.4   44.9 %   $ 20.9     $ 9.3   124.6 %
Operating loss   $ (3.3 )   $ (5.5 ) 40.4 %   $ (6.8 )   $ (18.8 ) 64.0 %
Consolidated                            
Net sales   $ 221.4     $ 297.6   (25.6 )%   $ 748.8     $ 1,122.8   (33.3 )%
Gross profit   $ 120.1     $ 166.4   (27.8 )%   $ 415.2     $ 645.0   (35.6 )%
Gross margin     54.3 %     55.9 %       55.4 %     57.4 %  
SG&A   $ 140.4     $ 148.7   (5.6 )%   $ 492.6     $ 566.1   (13.0 )%
SG&A as % of net sales     63.4 %     50.0 %       65.8 %     50.4 %  
Operating (loss) income   $ (16.6 )   $ 21.1   NM   $ (123.8 )   $ 93.7   NM
Operating margin     (7.5 )%     7.1 %       (16.5 )%     8.3 %  
(Loss) earnings before income taxes   $ (17.0 )   $ 21.0   NM   $ (125.9 )   $ 92.4   NM
Net (loss) earnings   $ (12.2 )   $ 15.3   NM   $ (95.7 )   $ 68.5   NM
Net (loss) earnings per diluted share   $ (0.74 )   $ 0.90   NM   $ (5.77 )   $ 4.05   NM
Weighted average shares outstanding – diluted     16.6       17.0   (2.3 )%     16.6       16.9   (2.0 )%

 

    Fourth Quarter     Full Year  
ADJUSTMENTS    
Fiscal 2020
   
Fiscal 2019
% Change    
Fiscal 2020
   
Fiscal 2019
% Change
LIFO adjustments(2)   $ 0.1     $ 0.6       $ (9.2 )   $ 1.5    
Tommy Bahama Japan inventory markdown charges (3)   $ 0.0     $ 0.2       $ 0.0     $ 0.2    
Lanier Apparel exit charges in cost of goods sold(4)   $ 0.3     $ 0.0       $ 6.7     $ 0.0    
Tommy Bahama Japan SG&A charges(5)   $ 0.0     $ 2.2       $ 0.0     $ 2.8    
Tommy Bahama information technology project write-off(6)   $ 15.5     $ 0.0       $ 15.5     $ 0.0    
Amortization of Lilly Pulitzer Signature Store intangible assets(7)   $ 0.1     $ 0.1       $ 0.3     $ 0.3    
Amortization of Southern Tide intangible assets(8)   $ 0.1     $ 0.1       $ 0.3     $ 0.3    
Southern Tide impairment charges(9)   $ 0.0     $ 0.0       $ 60.2     $ 0.0    
Lanier Apparel intangible asset impairment charges(10)   $ 0.0     $ 0.0       $ 0.2     $ 0.0    
Lanier Apparel exit charges in SG&A(11)   $ 2.6     $ 0.0       $ 6.3     $ 0.0    
TBBC change in fair value of contingent consideration(12)   $ 0.6     $ 0.4       $ 0.6     $ 0.4    
Impact of income taxes(13)   $ (4.8 )   $ (0.5 )     $ (15.2 )   $ (0.8 )  
Adjustment to net earnings(14)   $ 14.3     $ 3.1       $ 65.7     $ 4.6    
AS ADJUSTED                            
Tommy Bahama                            
Net sales   $ 142.7     $ 196.0   (27.2 )%   $ 419.8     $ 676.7   (38.0 )%
Gross profit   $ 82.5     $ 118.9   (30.6 )%   $ 244.2     $ 413.4   (40.9 )%
Gross margin   57.8 %   60.6 %   58.2 %   61.1 %  
Operating income (loss)   $ 5.4     $ 24.9   (78.1 )%   $ (37.8 )   $ 56.2   NM
Operating margin     3.8 %     12.7 %       (9.0 )%     8.3 %  
Lilly Pulitzer                            
Net sales   $ 54.4       64.9   (16.2 )%   $ 231.1     $ 284.7   (18.8 )%
Gross profit   $ 29.4       36.3   (19.1 )%   $ 138.0     $ 174.6   (21.0 )%
Gross margin   54.1 %   56.0 %   59.7 %   61.3 %  
Operating income   $ 2.1       5.2   (59.7 )%   $ 28.0     $ 52.1   (46.3 )%
Operating margin     3.8 %     8.0 %       12.1 %     18.3 %  
Southern Tide                            
Net sales   $ 7.5     $ 10.7   (29.7 )%   $ 34.7     $ 46.4   (25.3 )%
Gross profit   $ 3.9     $ 5.1   (24.0 )%   $ 11.8     $ 22.8   (48.2 )%
Gross margin   51.5 %   47.6 %   34.1 %   49.1 %  
Operating income (loss)   $ 0.1     $ 0.8   (89.4 )%   $ (4.3 )   $ 5.8   NM
Operating margin     1.1 %     7.0 %       (12.3 )%     12.6 %  
Lanier Apparel

(1)
                           
Net sales   $ 8.8     $ 19.8   (55.5 )%   $ 38.8     $ 95.2   (59.2 )%
Gross profit   $ 1.2     $ 3.9   (70.1 )%   $ 7.0     $ 25.1   (72.1 )%
Gross margin   13.1 %   19.5 %   18.0 %   26.4 %  
Operating (loss) income   $ (2.5 )   $ (1.8 ) (38.5 )%   $ (13.4 )   $ 2.0   NM
Operating margin     (28.1 )%     (9.0 )%       (34.6 )%     2.1 %  
Corporate and Other

(1)
                           
Net sales   $ 8.0     $ 6.1   30.1 %   $ 24.5     $ 19.8   23.4 %
Gross profit   $ 3.6     $ 3.1   16.5 %   $ 11.7     $ 10.8   8.7 %
Operating loss   $ (2.6 )   $ (4.4 ) (40.8 )%   $ (15.4 )   $ (16.9 ) (9.1 )%
Consolidated                            
Net sales   $ 221.4     $ 297.6   (25.6 )%   $ 748.8     $ 1,122.8   (33.3 )%
Gross profit   $ 120.5     $ 167.2   (28.0 )%   $ 412.7     $ 646.6   (36.2 )%
Gross margin     54.4 %     56.2 %       55.1 %     57.6 %  
SG&A   $ 121.6     $ 145.9   (16.7 )%   $ 469.7     $ 562.3   (16.5 )%
SG&A as % of net sales     54.9 %     49.0 %       62.7 %     50.1 %  
Operating income (loss)   $ 2.6     $ 24.7   (89.6 )%   $ (43.0 )   $ 99.1   NM
Operating margin     1.2 %     8.3 %       (5.7 )%     8.8 %  
Earnings (loss) before income taxes   $ 2.2     $ 24.6   NM   $ (45.0 )   $ 97.9   NM
Net earnings (loss)   $ 2.1     $ 18.5   NM   $ (30.0 )   $ 73.1   NM
Net earnings (loss) per diluted share   $ 0.13     $ 1.09   NM   $ (1.81 )   $ 4.32   NM

 

    Fourth Quarter   Fourth Quarter   Full Year
    Fiscal 2020   Fiscal 2019   Fiscal 2020   Fiscal 2019
    Actual   Actual   Actual   Actual
Net (loss) earnings per diluted share:                        
GAAP basis   $  
(0.74
)
  $ 0.90   $  
(5.77
)
  $ 4.05
LIFO adjustments(15)      
0.00
    0.03      
(0.39
)
    0.06
Amortization of recently acquired intangible assets(16)      
0.01
    0.01      
0.02
    0.03
Tommy Bahama Japan charges(17)      
0.00
    0.13      
0.00
    0.16
Tommy Bahama information technology project write-off(18)      
0.71
    0.00      
0.71
    0.00
Impairment of goodwill and intangible assets(19)      
0.00
    0.00      
3.02
    0.00
Lanier Apparel exit charges(20)      
0.12
    0.00      
0.57
    0.00
Change in fair value of contingent consideration(21)      
0.03
    0.02      
0.03
    0.02
As adjusted(14)   $  
0.13
  $ 1.09   $  
(1.81
)
  $ 4.32
                         
    First Quarter   First Quarter        
    Fiscal 2021   Fiscal 2020   Fiscal 2021   Fiscal 2020
    Guidance(22)   Actual   Guidance(22)   Actual
Net earnings per diluted share:                
GAAP basis   $ 0.90-1.10
  $ (4.02)   $  2.65-3.05     (5.77)
LIFO adjustments(15)      
0.00
    (0.12)      
0.00
    (0.39)
Amortization of recently acquired intangible assets(16)      
0.00
    0.01      
0.02
    0.02
Tommy Bahama information technology project write-off(18)      
0.00
    0.00      
0.00
    0.71
Impairment of goodwill and intangible assets(19)      
0.00
    3.02      
0.00
    3.02
Lanier Apparel exit charges(20)      
0.05
    0.00      
0.14
    0.57
Change in fair value of contingent consideration(21)      
0.00
    0.00      
0.00
    0.03
As adjusted(14)   $ 0.95-1.15
  $ (1.12)   $ 2.80-3.20
  $ (1.81)
                         
(1) As of the First Quarter of Fiscal 2020, the Duck Head(R) operations are included in Corporate and Other, whereas the operations were previously included in Lanier Apparel. Lanier Apparel and Corporate and Other amounts for prior periods have been restated to conform to the current period presentation.
(2) LIFO adjustments represents the impact on cost of goods sold resulting from LIFO accounting adjustments. These adjustments are included in Corporate and Other.
(3) Tommy Bahama Japan inventory markdown charges represents the inventory markdown impact on cost of goods sold resulting from the restructuring and exit of the Tommy Bahama Japan operations, which was completed in the first half of Fiscal 2020. These charges are included in cost of goods sold in Tommy Bahama.
(4) Lanier Apparel exit charges in cost of goods sold relate to the Third Quarter of Fiscal 2020 decision to exit the Lanier Apparel business, which is expected to be completed during the Second Half of Fiscal 2021. These charges consist of inventory markdowns and charges related to the Merida manufacturing facility, which ceased operations in Fiscal 2020. These charges are included in cost of goods sold in Lanier Apparel.
(5) Tommy Bahama Japan SG&A charges represents the SG&A impact of the restructuring and exit of the Tommy Bahama Japan operations, which was completed in the First Half of Fiscal 2020. These charges are included in SG&A in Tommy Bahama.
(6) Tommy Bahama information technology project write-off represents a charge for the write-off of previously capitalized costs related to a project that was abandoned in the Fourth Quarter of Fiscal 2020. This charge is included in SG&A in Tommy Bahama.
(7) Amortization of Lilly Pulitzer Signature Store intangible assets represents the amortization related to intangible assets acquired as part of Lilly Pulitzer’s acquisition of certain Lilly Pulitzer Signature Stores. These charges are included in SG&A in Lilly Pulitzer.
(8) Amortization of Southern Tide intangible assets represents the amortization related to intangible assets acquired as part of the Southern Tide acquisition. These charges are included in SG&A in Southern Tide.
(9) Southern Tide impairment charges represents the impairment related to goodwill and intangible assets related to Southern Tide. These charges are included in impairment of goodwill and intangible assets in Southern Tide.
(10) Lanier Apparel intangible asset impairment charges represents the impairment related to a trademark acquired in a prior year. This charge is included in impairment of goodwill and intangible assets in Lanier Apparel.
(11) Lanier Apparel exit charges in SG&A relate to the Third Quarter of Fiscal 2020 decision to exit the Lanier Apparel business. These charges consist of operating lease asset impairment charges, employee charges, and fixed asset impairment charges. These charges are included in SG&A in Lanier Apparel.
(12) TBBC change in fair value of contingent consideration represents the impact related to the change in the fair value of contingent consideration related to the TBBC acquisition. These charges are included in SG&A in Corporate and Other.
(13) Impact of income taxes represents the estimated tax impact of the above adjustments based on the estimated effective tax rate on current year earnings in the respective jurisdiction.
(14) Amounts in columns may not add due to rounding.
(15) LIFO adjustments represents the impact, net of income taxes, on net (loss) earnings per diluted share resulting from LIFO accounting adjustments. No estimate for LIFO accounting adjustments is reflected in the guidance for any future periods.
(16) Amortization of recently acquired intangible assets represents the impact, net of income taxes, on net (loss) earnings per diluted share resulting from the amortization of intangible assets acquired as part of the Lilly Pulitzer Signature Store and Southern Tide acquisitions.
(17) Tommy Bahama Japan charges represents the impact, net of income taxes, on net (loss) earnings per diluted share of the restructuring and exit of the Tommy Bahama Japan operations.
(18) Tommy Bahama information technology project write-off represents the impact, net of income taxes, on net (loss) earnings per diluted share resulting from a charge for the write-off of previously capitalized costs related to a project that was abandoned in the Fourth Quarter of Fiscal 2020
(19) Impairment of goodwill and intangible assets represents the impact, net of income taxes, on net (loss) earnings per diluted share resulting from the impairment charges in Southern Tide and Lanier Apparel. Due to the non-deductibility of $18 million of Southern Tide goodwill amounts, the effective tax rate on these impairment charges for goodwill and intangible assets was 17%.
(20) Lanier Apparel exit charges represents the impact, net of income taxes, on net (loss) earnings per diluted share resulting from the Third Quarter of Fiscal 2020 decision to exit the Lanier Apparel.
(21) Change in fair value of contingent consideration represents the impact, net of income taxes, on net (loss) earnings per diluted share relating to the change in the fair value of contingent consideration related to the TBBC acquisition.
(22) Guidance as issued on March 25, 2021.

 

Location Count
  Beginning of Year End of Q1 End of Q2 End of Q3 End of Q4
Fiscal 2020          
Tommy Bahama          
Full-price retail store 111 110 107 106 105
Retail-restaurant 16 18 19 19 20
Outlet 35 35 35 35 35
Total Tommy Bahama 162 163 161 160 160
Lilly Pulitzer 61 61 59 59 59
Southern Tide 1 1 2 3 3
Oxford Total 224 225 222 222 222
Fiscal 2019          
Tommy Bahama          
Full-price retail store 113 113 113 111 111
Retail-restaurant 17 17 17 17 16
Outlet 37 37 37 37 35
Total Tommy Bahama 167 167 167 165 162
Lilly Pulitzer 62 63 63 63 61
Southern Tide 1
Oxford Total 229 230 230 228 224
 

 



Trevi Therapeutics Announces Fourth Quarter and Year End 2020 Financial Results and Business Updates

Expects to Complete Enrollment and Report Top-Line Data of the Phase 2b/3 PRISM Trial in Second Half of 2021

Cash Position Expected to Fund Operations into the Second Quarter of 2022

NEW HAVEN, Conn., March 25, 2021 (GLOBE NEWSWIRE) — Trevi Therapeutics, Inc. (Nasdaq: TRVI), a clinical-stage biopharmaceutical company focused on the development and commercialization of Haduvio™ (nalbuphine ER) to treat serious neurologically mediated conditions, today announced financial results for the quarter and year ended December 31, 2020, as well as business highlights.

“We made significant progress in the PRISM trial this year, despite the impact of COVID-19 which slowed recruitment activities worldwide through the latter part of 2020 and early 2021. Recruiting for this trial has accelerated this month and we expect to complete enrollment in the third quarter of this year and report top-line results in the fourth quarter of 2021,” said Jennifer L. Good, President and CEO of Trevi Therapeutics. “Throughout this past year, we have added to our key talent as we progress through the clinical development of Haduvio in two important indications and prepare for the next phase of development.”

Key Business Updates

  • Phase 2b/3 PRISM trial of Haduvio for severe pruritus in patients with prurigo nodularis (PN): To date, the Company has enrolled approximately 240 of the 360 planned total subjects in the trial and reaffirms expectations that enrollment will be completed in the third quarter of 2021 and top-line data will be reported in the fourth quarter of 2021.
  • Phase 2 CANAL trial of Haduvio for chronic cough in patients with idiopathic pulmonary fibrosis (IPF): This trial is currently being conducted in the United Kingdom, which resumed its shelter in place directive due to COVID-19 in early December 2020 through the end of March 2021. The restrictions paused enrollment for this at-risk patient group during the related time period. We expect to resume recruiting subjects for the trial in the second quarter of 2021. Trevi is also seeking regulatory and ethics board approvals to add study sites in Germany.

Fourth Quarter 2020 Financial Highlights

Research and development (R&D) expenses: R&D expenses for the fourth quarter of 2020 were $6.6 million compared to $4.8 million in the same period in 2019. The increase was primarily due to increased activity in the Company’s Phase 2b/3 PRISM clinical trial as well as expenses associated with the purchase of clinical trial supplies.

General and administrative (G&A) expenses: G&A expenses for the fourth quarter of 2020 were $2.6 million compared to $1.9 million in the same period in 2019. The increase was primarily due to an increase in consulting fees and stock-based compensation expenses.

Net loss: For the fourth quarter of 2020, the Company reported a net loss of $9.5 million, compared to a net loss of $6.5 million in the same period in 2019.

Year End 2020 Financial Highlights

Cash position: As of December 31, 2020, total cash and cash equivalents were $45.0 million compared to $57.3 million as of December 31, 2019. Trevi believes its current cash position will be sufficient to fund operations into the second quarter of 2022.

R&D expenses: R&D expenses for the year ended December 31, 2020 were $22.3 million compared to $19.3 million for the year ended December 31, 2019. The increase was primarily due to an increase in clinical development expenses, primarily related to increased activity and enrollment in the Phase 2b/3 PRISM trial as well as an increase in expenses related to the purchase of clinical trial supplies.

G&A expenses: G&A expenses for the year ended December 31, 2020 were $10.2 million compared to $7.3 million for the year ended December 31, 2019. The increase was primarily due to an increase in stock-based compensation expenses attributable to the issuance of new stock option grants in connection with the IPO and in the first quarter of 2020, increased consulting fees as well as increased expenses related to being a public company.

Net loss: For the year ended December 31, 2020, Trevi reported a net loss of $32.8 million compared to a net loss of $26.1 million for the year ended December 31, 2019.

Conference Call

As previously announced, the Company will host a conference call and webcast today, March 25, 2021 at 4:30 p.m. ET. To participate in the live conference call by phone, please dial (866) 360-5746 (domestic) or (602) 563-8605 (international) and provide access code 8599904. A live audio webcast will be accessible from the ‘Investors & News’ section on the Company’s website at www.trevitherapeutics.com. An archived replay of the webcast will also be available for 30 days on the Company’s website following the event.

About Trevi Therapeutics, Inc.

Trevi Therapeutics, Inc. is a clinical-stage biopharmaceutical company focused on the development and commercialization of Haduvio to treat serious neurologically mediated conditions. Trevi is conducting a Phase 2b/3 clinical trial of Haduvio for the treatment of chronic pruritus associated with prurigo nodularis and a Phase 2 trial for chronic cough in patients with idiopathic pulmonary fibrosis (IPF). Trevi is also developing Haduvio for the treatment of levodopa-induced dyskinesia (LID) in patients with Parkinson’s disease and is in the planning stages of a Phase 2 study in this indication. These conditions share a common pathophysiology that is mediated through opioid receptors in the central and peripheral nervous systems.

Founded in 2011, Trevi Therapeutics is headquartered in New Haven, CT.

About HADUVIO

Haduvio is an oral extended release formulation of nalbuphine. Nalbuphine is a mixed ĸ-opioid receptor agonist and µ-opioid receptor antagonist that has been approved and marketed as an injectable for pain indications for more than 20 years in the United States and Europe. The ĸ- and µ-opioid receptors are known to be critical mediators of itch, cough and certain movement disorders. Nalbuphine’s mechanism of action also mitigates the risk of abuse associated with µ-opioid agonists because it antagonizes, or blocks, µ-opioid receptors. Nalbuphine is currently the only opioid approved for marketing that is not classified as a controlled substance in the United States and most of Europe. Trevi intends to propose Haduvio as the trade name for the nalbuphine ER investigational product. Haduvio is an investigational drug product and its safety and efficacy have not been fully evaluated by any regulatory authority.

Forward-Looking Statements

Statements contained in this press release regarding matters that are not historical facts are “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995. Such statements are subject to risks and uncertainties and actual results may differ materially from those expressed or implied by such forward-looking statements. Such statements include, but are not limited to, statements regarding the impact of the COVID-19 pandemic on Trevi’s clinical trials, business and operations; the expected timing of enrollment and for reporting top-line data from Trevi’s Phase 2b/3 PRISM trial of Haduvio in patients with prurigo nodularis; Trevi’s business plans and objectives, including future plans or expectations for Trevi’s product candidates; expectations regarding Trevi’s uses and sufficiency of capital; and other statements containing the words “believes,” “anticipates,” “plans,” “expects,” and similar expressions. Risks that contribute to the uncertain nature of the forward-looking statements include: uncertainties regarding the success, cost and timing of Trevi’s product candidate development activities and ongoing and planned clinical trials; uncertainties regarding the scope, timing and severity of the COVID-19 pandemic, the impact of the COVID-19 pandemic on Trevi’s clinical operations and actions taken in response to the pandemic; uncertainties regarding Trevi’s ability to execute on its strategy; the risk that positive results from a clinical trial may not necessarily be predictive of the results of future or ongoing clinical trials; potential regulatory developments in the United States and foreign countries; uncertainties inherent in estimating Trevi’s cash runway, future expenses and other financial results; as well as other risks and uncertainties set forth in the quarterly report on Form 10-Q for the quarter ended September 30, 2020 filed with the Securities and Exchange Commission and in subsequent filings with the Securities and Exchange Commission. All forward-looking statements contained in this press release speak only as of the date on which they were made. Trevi undertakes no obligation to update such statements to reflect events that occur or circumstances that exist after the date on which they were made.

Trevi Therapeutics, Inc.

Selected Balance Sheet Data

(unaudited)

(amounts in thousands)

  December 31,

2020
  December 31,

2019
       
Cash and cash equivalents $ 45,001     $ 57,313  
Working capital   40,714       54,353  
Total assets   47,131       60,001  
Total debt   13,954       ──  
Stockholders’ equity   27,282       54,545  



Trevi Therapeutics, Inc.

Selected Statement of Operations Data

(unaudited)

(amounts in thousands)

  Three Months Ended

December 31,
  Year Ended

December 31,
    2020       2019       2020       2019  
Operating expenses:                               
Research and development $ 6,560     $ 4,823     $ 22,328     $ 19,339  
General and administrative   2,633       1,943       10,161       7,306  
Total operating expenses   9,193       6,766       32,489       26,645  
Loss from operations   (9,193 )     (6,766 )     (32,489 )     (26,645 )
Other income (expense), net   (313 )     225       (287 )     577  
Loss before income tax benefit   (9,506 )     (6,541 )     (32,776 )     (26,068 )
Income tax benefit (expense)   (17 )     4       18       18  
Net loss $ (9,523 )   $ (6,537 )   $ (32,758 )   $ (26,050 )



Investor Contact

Eric Ribner
LifeSci Advisors
917 592 0932
[email protected]

Media Contact

Rosalia Scampoli
914-815-1465
[email protected]



Alector to Present at Stifel’s 3rd Annual CNS Day

SOUTH SAN FRANCISCO, Calif., March 25, 2021 (GLOBE NEWSWIRE) — Alector, Inc. (Nasdaq: ALEC), a clinical-stage biotechnology company pioneering immuno-neurology, today announced that Shehnaaz Suliman, M.D., MBA, M.Phil., president and chief operating officer of Alector, will participate in a fireside chat at Stifel’s 3rd Annual CNS Day on Thursday, April 1, 2021, at 9:30 a.m. ET.

A live webcast of the fireside chat will be available on the “Events & Presentations” page within the Investors section of the Alector website at http://investors.alector.com. A replay will be available on the Alector website for 30 days following the event.

About Alector

Alector is a clinical stage biotechnology company pioneering immuno-neurology, a novel therapeutic approach for the treatment of neurodegenerative diseases. The Company is developing a broad portfolio of innate immune system programs, designed to functionally repair genetic mutations that cause dysfunction of the brain’s immune system and enable the rejuvenated immune cells to counteract emerging brain pathologies. Immuno-neurology targets immune dysfunction as a root cause of multiple pathologies that are drivers of degenerative brain disorders. The Company’s immuno-neurology product candidates are supported by biomarkers and target genetically defined patient populations in frontotemporal dementia and Alzheimer’s disease. This scientific approach is also the basis for the Company’s immuno-oncology programs. Alector is headquartered in South San Francisco, California. For additional information, please visit www.alector.com.

Contacts

Media:
Erica Jefferson
Vice President, Communications and Public Affairs
Alector, Inc.
301-928-4650
[email protected]

1AB
Dan Budwick
973-271-6085
[email protected]

or

Investors:
Alector, Inc.
[email protected]



Zealand Pharma to participate in upcoming investor conferences

Company announcement – No. 17 / 2020

Zealand Pharma to participate in upcoming investor conferences

Copenhagen, DK and Boston, MA, U.S.
March 25, 2021 – Zealand Pharma A/S (Nasdaq: ZEAL) (CVR-no. 20045078), a biotechnology company focused on the discovery, development and commercialization of innovative peptide-based medicines, today announced that members of its senior management team are scheduled to participate virtually in the following investor conferences in April:

Guggenheim Virtual Healthcare Talks – Genomic Medicines & Rare Disease
Date: Thursday, April 1, 2021
 
20th Annual Virtual Needham Healthcare Conference  
Date: Monday, April 12, 2021  
Presentation: 11:45 a.m. ET/ 4:45 p.m. CET


A live webcast of the Needham event will be available on the “Events & Presentations” page in the Investor section of the Company’s website at https://www.zealandpharma.com/events-presentations. A replay of the webcast will be archived on the Company’s website following the presentation.

# # #

About Zealand Pharma A/S

Zealand Pharma A/S (Nasdaq: ZEAL) (“Zealand”) is a biotechnology company focused on the discovery, development, and commercialization of next generation peptide-based medicines that change the lives of people living with metabolic and gastrointestinal diseases. More than 10 drug candidates invented by Zealand have advanced into clinical development, of which two have reached the market. Zealand’s robust pipeline of investigational medicines includes three candidates in late stage development, and one candidate being reviewed for regulatory approval in the United States. Zealand markets V-Go®, an all-in-one basal-bolus insulin delivery option for people with diabetes. License collaborations with Boehringer Ingelheim and Alexion Pharmaceuticals create opportunity for more patients to potentially benefit from Zealand-invented peptide therapeutics. Zealand was founded in 1998 in Copenhagen, Denmark, and has presence throughout the U.S. that includes key locations in New York, Boston, and Marlborough (MA). For more information about Zealand’s business and activities, please visit http://www.zealandpharma.com.

For further information, please contact:

Zealand Pharma Investor Relations

Claudia Styslinger
Argot Partners
[email protected]

Zealand Pharma Media Relations

David Rosen
Argot Partners
[email protected]



Viridian Therapeutics Reports 2020 Financial Results and Provides Corporate Updates

  • Progressed lead programs VRDN-001 and VRDN-002 towards clinical trials in Thyroid Eye Disease (TED); both IND filings expected by the end of 2021
  • Completed integration and name change to Viridian Therapeutics following October 2020 merger and concurrent financing
  • Ended 2020 with a strong cash position of $127.6 million, and runway into the second half of 2023
  • Strengthened leadership team with the appointment of Dr. Jonathan Violin as CEO and additions of Dr. Barrett Katz as CMO and Dr. Vahe Bedian as Chief Scientist

BOULDER, Colo., March 25, 2021 (GLOBE NEWSWIRE) — Viridian Therapeutics, Inc. (NASDAQ: VRDN), a biopharmaceutical company advancing new treatments for patients suffering from serious diseases but underserved by today’s therapies, today announced financial results for the fourth quarter and year ended December 31, 2020 and provided corporate updates.

“2020 was a transformative year for Viridian. We completed the acquisition of private Viridian Therapeutics and a concurrent financing, revamped our business and added $115.0 million to our balance sheet in the fourth quarter. We have also strengthened our management team and now have multiple product candidates with the potential to become meaningful treatments for patients suffering from TED,” said Jonathan Violin, Ph.D., President and Chief Executive Officer of Viridian. “As we enter 2021, we look forward to reaching important R&D milestones in our TED programs, continuing to build out our team and expanding our pipeline beyond TED.”

Recent Highlights


  • Jonathan Violin, Ph.D. appointed President, CEO and Director
    – Dr. Violin co-founded privately-held Viridian Therapeutics, which was acquired by the Company in October 2020. Dr. Violin also founded and served as CEO of two drug discovery companies, Quellis Biosciences and Dianthus Therapeutics, and co-founded and held several executive positions at Trevena, Inc.


  • Barrett Katz M.D. joined Viridian as Chief Medical Officer (CMO)
    – Dr. Katz is an internationally recognized neuro-ophthalmologist. He comes to Viridian from BridgeBio Pharma, Inc. where he developed therapeutics to treat orphan eye diseases. Prior to BridgeBio, he was CMO at GenSight Biologics where he oversaw early- and late-stage clinical programs.


  • Vahe Bedian, Ph.D. appointed as Chief Scientist
    – Dr. Bedian co-founded privately-held Viridian Therapeutics. Dr. Bedian also co-founded and served as Chief Scientific Officer of Quellis Biosciences and Dianthus Therapeutics. He also previously held leadership positions in therapeutic antibody research and development at AstraZeneca and Pfizer.


  • Changed Company name to Viridian Therapeutics
    –The new name reflects the evolution of the Company and its patient-centric model of innovation.

Development Pipeline Overview and Update

Viridian is developing multiple product candidates to treat patients who suffer from thyroid eye disease (TED), a debilitating auto-immune disease that causes inflammation and fibrosis of the orbit and tissues surrounding the eye which can lead to proptosis, or bulging of the eyes, redness and swelling, double vision, pain, and potential blindness. TED significantly impacts quality of life, imposing a high physical and mental burden on patients. There is currently one Food and Drug Administration (FDA)-approved treatment for TED, which is an intravenously administered monoclonal antibody that targets the insulin-like growth factor-1 receptor (IGF-1R).

Viridian’s most advanced product candidate is VRDN-001, an intravenously administered anti-IGF-1R monoclonal antibody licensed from ImmunoGen, Inc. This antibody had previously been developed in oncology as AVE-1642 and studied in over 100 patients. The pharmacokinetics, pharmacodynamics, safety, and tolerability data from that clinical program has informed the Company’s plans to further evaluate VRDN-001 in TED. Manufacturing is underway and the Company expects to file an IND in the fourth quarter of 2021, with initial proof of concept data in patients expected in the second quarter of 2022.

Viridian’s second product candidate, VRDN-002, is a distinct anti-IGF-1R antibody that incorporates half-life extension technology and is intended for subcutaneous administration. VRDN-002 manufacturing is underway, and the Company expects to file an IND before the end of 2021. The Company expects to initiate clinical development with a Phase 1 single ascending dose trial to explore safety, tolerability, pharmacokinetics, and target engagement of VRDN-002 in healthy volunteers. Data from this trial is expected in mid-year 2022 and the Company expects to initiate the dosing of patients later in 2022.

Viridian is also pursuing multiple hypotheses within the VRDN-003 program that may offer additional improvements to the class of IGF-1R targeted therapeutic antibodies. In addition, the Company continues to advance its efforts beyond IGF-1R and TED and is focused on opportunities that will leverage validated mechanisms, technologies, and modalities to bring new therapeutic options to patients underserved by today’s options. The most advanced of these programs is VRDN-004, a therapeutic antibody program currently in discovery stage. The Company also continues to evaluate other targets and indications for a future VRDN-005 program.

2020 Financial Results

Cash Position and Runway: Cash, cash equivalents and short-term investments were $127.6 million as of December 31, 2020, compared to $30.1 million as of September 30, 2020 and $26.8 million as of December 31, 2019. Viridian believes that its current cash, cash equivalents and short-term investments will be sufficient to fund its operations into the second half of 2023.

Revenue: Revenue was $0.1 million during the fourth quarter and $1.1 million for the year ended December 31, 2020, compared to $0.9 million and $4.5 million, respectively for the comparable periods in 2019. The decrease in revenue was primarily due to a decrease in research and development activities related to legacy microRNA assets that were reimbursable to the Company under a prior collaboration agreement.

Research and Development Expenses: Research and development expenses were $15.3 million for the fourth quarter of 2020 and $28.3 million for the year ended December 31, 2020, compared to $8.4 million and $34.8 million, respectively for the comparable periods in 2019. The increase in research and development expenses during the fourth quarter was primarily attributable to increased license fees related to the Company’s license agreement with Xencor. The year over year decrease in research and development expenses was primarily attributable to a decrease in clinical and related manufacturing development activities primarily associated with the Company’s legacy microRNA programs and decreases in personnel related costs including restructuring charges in 2020. These decreases were partially offset by an increase in licensing fees primarily attributable to the Company’s license agreement with Xencor.

Acquired In-Process Research and Development (IPR&D) Expense: Acquired IPR&D expense was $69.9 million during the fourth quarter of 2020 and for the year ended December 31, 2020. IPR&D expense resulted from the acquisition of private Viridian Therapeutics in October 2020. The acquisition cost allocated to acquired IPR&D with no alternative future use was recorded as expense at the acquisition date. No acquired IPR&D expenses were incurred in 2019.

General and Administrative Expenses: General and administrative expenses were $5.5 million for the fourth quarter of 2020 and $13.3 million for the year ended December 31, 2020, compared to $2.5 million and $11.6 million, respectively for the comparable periods in 2019. The fourth quarter and year over year increases in general and administrative expenses were due primarily to increases in professional and personnel related costs, including consulting and contract labor.

Net Loss: The Company’s net loss was $90.7 million, or $23.07 per share, for the fourth quarter of 2020, and $110.7 million, or $31.13 per share for the year ended December 31, 2020, compared to $10.1 million, or $4.69 per share, for the fourth quarter of 2019 and $41.9 million, or $20.04 per share for the year ended December 31, 2019.

Shares Outstanding: As of March 15, 2021, Viridian had 30,886,700 shares of common stock outstanding on an as-converted basis, which included 7,230,651 shares of common stock and 23,656,049 shares of common stock issuable upon the conversion of 354,823 shares of preferred stock.

Conference Call Information

The Viridian Therapeutics management team will host a conference call and webcast today at 4:30 p.m. ET to provide corporate updates and discuss the Company’s financial results for the fourth quarter and year ended December 31, 2020. To access the call, please dial 877-407-0789 (domestic) or 201-689-8562 (international) and provide the passcode 13717079. A live webcast of the call will be available on the Investors section of the Viridian Therapeutics website at www.viridiantherapeutics.com and a replay of this conference call will be available approximately one hour after its completion.

About Viridian Therapeutics, Inc.

Viridian Therapeutics is a biotechnology company advancing new treatments for patients suffering from serious diseases but underserved by today’s therapies. Viridian’s most advanced program, VRDN-001, is an anti-IGF-1R monoclonal antibody in development for thyroid eye disease (TED), a debilitating auto-immune disease that causes inflammation and fibrosis within the orbit of the eye which can cause double vision, pain, and potential blindness. Patients with severe disease often require multiple remedial surgeries to the orbit, eye muscles and eyelids Viridian is based in Boulder, Colorado, and Waltham, Massachusetts. Learn more about Viridian and our programs at www.viridiantherapeutics.com.

Follow us on Twitter @ViridianThera and on LinkedIn.

Note Regarding Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. These statements may be identified by the use of words such as, but not limited to, “anticipate,” “believe,” “continue,” “could,” “estimate,” “expect,” “intend,” “may,” “might,” “plan,” “potential,” “predict,” “project,” “should,” “target,” “will,” or “would” or other similar terms or expressions that concern Viridian’s expectation, strategy, plans and intentions. Forward-looking statements include, without limitation, statements regarding the Company’s expectations and guidance regarding its business plans and objectives for its product candidates, including the therapeutic potential and clinical benefits thereof, and pipeline, projected cash runway, the timing, progress and plans for the Company’s ongoing and future research and clinical development programs, future regulatory interactions, expectations regarding the timing for data, and the timing of the Company’s IND filings for VRDN-001 and VRDN-002. Forward-looking statements are neither historical facts nor assurances of future performance. Instead, they are based on our current beliefs, expectations and assumptions regarding the future of our business, future plans and strategies, our clinical results and other future conditions. New risks and uncertainties may emerge from time to time, and it is not possible to predict all risks and uncertainties. No representations or warranties (expressed or implied) are made about the accuracy of any such forward-looking statements. We may not actually achieve the forecasts disclosed in our forward-looking statements, and you should not place undue reliance on our forward-looking statements. Such forward-looking statements are subject to a number of material risks and uncertainties including but not limited to the effects from the COVID-19 pandemic on the company’s clinical activities, business and operating results; uncertainty and potential delays related to clinical drug development; smaller than anticipated market opportunities for the company’s product candidates; manufacturing risks; competition from other therapies or products; other matters that could affect the sufficiency of existing cash, cash equivalents and short-term investments to fund operations; the company’s future operating results and financial performance; the timing of pre-clinical and clinical trial activities and reporting results from same; and those risks set forth under the caption “Risk Factors” in the Company’s Quarterly Report on Form 10-Q filed with the Securities and Exchange Commission (SEC) on November 12, 2020 and other subsequent disclosure documents filed with the SEC. Any forward-looking statement speaks only as of the date on which it was made. Neither we, nor our affiliates, advisors or representatives, undertake any obligation to publicly update or revise any forward-looking statement, whether as a result of new information, future events or otherwise, except as required by law. These forward-looking statements should not be relied upon as representing our views as of any date subsequent to the date hereof.

Viridian Contacts:

Investors:

Dan Ferry
LifeSci Advisors
617-430-7576
[email protected]

Media:

Darby Pearson
Verge Scientific Communications
703-587-0831
[email protected]

 
Viridian Therapeutics, Inc.

Condensed Consolidated Statements of Operations and Comprehensive Loss

(in thousands, except share and per share data)

(unaudited)
         
    Three Months Ended

December 31,
  Year Ended

December 31,
    2020   2019   2020   2019
Revenue:                
Collaboration revenue   $ 54     $ 837     $ 735     $ 4,308  
Grant revenue       43     315     153  
Total revenue   54     880     1,050     4,461  
Operating expenses:                
Research and development   15,254     8,417     28,304     34,794  
General and administrative   5,537     2,534     13,265     11,646  
Acquired in-process research and development   69,861         69,861      
Total operating expenses   90,652     10,951     111,430     46,440  
Loss from operations   (90,598 )   (10,071 )   (110,380 )   (41,979 )
Other income (expense):                
Interest and other income   36     123     173     941  
Interest and other expense   (180 )   (170 )   (508 )   (835 )
Net loss   (90,742 )   (10,118 )   (110,715 )   (41,873 )
Change in unrealized gain (loss) on investments       (3 )   (8 )   3  
Comprehensive loss   $ (90,742 )   $ (10,121 )   $ (110,723 )   $ (41,870 )
                 
Net loss   $ (90,742 )   $ (10,118 )   $ (110,715 )   $ (41,873 )
Net loss per share, basic and diluted   $ (23.07 )   $ (4.69 )   $ (31.13 )   $ (20.04 )
Weighted-average shares used to compute basic and diluted net loss per share   3,932,917     2,158,695     3,557,065     2,089,094  
                         

 
Viridian Therapeutics, Inc.

Selected Financial Information

Condensed Consolidated Balance Sheet Data

(amounts in thousands)

(unaudited)
   
  December 31,
  2020   2019
       
Cash and cash equivalents $ 45,897     $ 24,846  
Short-term investments $ 81,742     $ 1,999  
Total assets $ 131,255     $ 30,262  
Notes payable, inclusive of current portion $     $ 8,304  
Total liabilities $ 11,218     $ 14,508  
Total stockholders’ equity $ 120,037     $ 15,754  
               



Phunware Reports Full Year 2020 Financial Results

AUSTIN, Texas, March 25, 2021 (GLOBE NEWSWIRE) — Phunware, Inc. (NASDAQ: PHUN) (“Phunware” or “the Company”), a fully-integrated enterprise cloud platform for mobile that provides products, solutions, data and services for brands worldwide, today announced financial results for its full year ended December 31, 2020.

“This past year was the genesis of an inflection point in our company’s history, as we shifted from a non-recurring, low margin transaction business to a far stickier, more scalable, recurring and high margin SaaS licensing business for our Multiscreen-as-a-Service (“MaaS”) platform,” said Alan S. Knitowski, President, CEO and Co-Founder of Phunware. “In addition to continued enterprise interest in our MaaS Digital Front Door solution for healthcare and our MaaS Smart Workplace solution for corporations, we have resumed conversations with customers from sectors that were hard hit by the pandemic, including the hospitality and real estate verticals. In conjunction with growing our portfolio of direct customers, we intend to expand our footprint globally by amplifying our go-to-market strategy with indirect sales and channel partners, including an anchor distribution partner that will be formally announced during Q2. In parallel, we are excited about the completion of PhunWallet next month as we launch our blockchain ecosystem powered by PhunCoin and PhunToken. We are on schedule to commercialize, scale and monetize this part of our business and look forward to the accelerated global adoption of our blockchain-enabled MaaS Customer Data Platform and MaaS Mobile Loyalty Ecosystem alike.”


Full Year 2020 Summary Financial Highlights

  • Net Revenues for the year totaled $10.0 million
  • Multiscreen-as-a-Service (MaaS) Platform Subscriptions and Services Revenues were $9.1 million
  • Gross Margin was 66.4%
  • Net Loss was ($22.2) million
  • Net Loss per Share was ($0.50)
  • Non-GAAP Adjusted EBITDA Loss was ($8.4) million

“Our executive team continues to proactively attend well-respected financial conferences and meetings with accredited institutional investors in order to bolster our corporate profile within the capital markets,” said Matt Aune, CFO of Phunware. “With a robust cash position as a result of our recently completed institutional financing of approximately $25 million, we now have the financial flexibility to execute both our near-term and long-term operational initiatives.”


Recent Business Highlights


Conference Call Information

Phunware management will host a conference call today (March 25, 2021) at 5:00 p.m. Eastern Time (2:00 p.m. Pacific Time) to discuss its financial results for the full year ended December 31, 2020.

Interested parties may access the conference call by dialing (888) 506-0062 in the United States, or (973) 528-0011 from international locations. The conference call will be broadcast live and available for replay here and via the investor relations section of the Company’s website at investors.phunware.com.

Safe Harbor Clause and Forward-Looking Statements

This press release includes forward-looking statements. All statements other than statements of historical facts contained in this press release, including statements regarding our future results of operations and financial position, business strategy and plans, and our objectives for future operations, are forward-looking statements. The words “anticipate,” “believe,” “continue,” “could,” “estimate,” “expect,” “expose,” “intend,” “may,” “might,” “opportunity,” “plan,” “possible,” “potential,” “predict,” “project,” “should,” “will,” “would” and similar expressions that convey uncertainty of future events or outcomes are intended to identify forward-looking statements, but the absence of these words does not mean that a statement is not forward-looking.

The forward-looking statements contained in this press release are based on our current expectations and beliefs concerning future developments and their potential effects on us. Future developments affecting us may not be those that we have anticipated. These forward-looking statements involve a number of risks, uncertainties (some of which are beyond our control) and other assumptions that may cause actual results or performance to be materially different from those expressed or implied by these forward-looking statements. These risks and uncertainties include, but are not limited to, those factors described under the heading “Risk Factors” in our filings with the Securities and Exchange Commission (the “SEC”), including our reports on Forms 10-K, 10-Q, 8-K and other filings that we make with the SEC from time to time. Should one or more of these risks or uncertainties materialize, or should any of our assumptions prove incorrect, actual results may vary in material respects from those projected in these forward-looking statements. We undertake no obligation to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise, except as may be required under applicable securities laws. These risks and others described under “Risk Factors” in our SEC filings may not be exhaustive.

By their nature, forward-looking statements involve risks and uncertainties because they relate to events and depend on circumstances that may or may not occur in the future. We caution you that forward-looking statements are not guarantees of future performance and that our actual results of operations, financial condition and liquidity, and developments in the industry in which we operate may differ materially from those made in or suggested by the forward-looking statements contained in this press release. In addition, even if our results or operations, financial condition and liquidity, and developments in the industry in which we operate are consistent with the forward-looking statements contained in this press release, those results or developments may not be indicative of results or developments in subsequent periods.

Disclosure Information

Phunware uses and intends to continue to use its Investor Relations website as a means of disclosing material nonpublic information and for complying with its disclosure obligations under Regulation FD. Accordingly, investors should monitor the Company’s Investor Relations website, in addition to following the Company’s press releases, SEC filings, public conference calls, presentations and webcasts.

About Phunware, Inc.

Everything You Need to Succeed on Mobile — Transforming Digital Human Experience


Phunware, Inc. (NASDAQ: PHUN)
, is the pioneer of Multiscreen-as-a-Service (MaaS), an award-winning, fully integrated enterprise cloud platform for mobile that provides companies the products, solutions, data and services necessary to engage, manage and monetize their mobile application portfolios and audiences globally at scale. Phunware’s Software Development Kits (SDKs) include location-based services, mobile engagement, content management, messaging, advertising, loyalty (PhunCoin & Phun) and analytics, as well as a mobile application framework of pre-integrated iOS and Android software modules for building in-house or channel-based mobile application and vertical solutions. Phunware helps the world’s most respected brands create category-defining mobile experiences, with more than one billion active devices touching its platform each month. For more information about how Phunware is transforming the way consumers and brands interact with mobile in the virtual and physical worlds, visit https://www.phunware.com, https://www.phuncoin.com, https://www.phuntoken.com, and follow @phunware, @phuncoin and @phuntoken on all social media platforms.

Phunware PR & Media Inquiries:

Email: [email protected]
Phone: (512) 693-4199

Phunware Investor Relations:

Matt Glover and John Yi
Gateway Investor Relations
Email: [email protected]
Phone: (949) 574-3860



Consolidated Balance Sheets

(In thousands, except per share information)

  December 31,

2020
  December 31,

2019
Assets      
Current assets:      
Cash $ 3,940       $ 276    
Accounts receivable, net of allowance for doubtful accounts of $356 and $3,179 at December 31, 2020 and 2019, respectively 664       1,671    
Prepaid expenses and other current assets 304       368    
Total current assets 4,908       2,315    
Property and equipment, net 13       24    
Goodwill 25,900       25,857    
Intangible assets, net 111       253    
Deferred tax asset 537       241    
Restricted cash 91       86    
Other assets 276       276    
Total assets 31,836       29,052    
Liabilities and stockholders’ equity (deficit)      
Current liabilities:      
Accounts payable $ 8,462       $ 10,159    
Accrued expenses 5,353       4,035    
Accrued legal settlement 3,000          
Deferred revenue 2,397       3,360    
PhunCoin deposits 1,202       1,202    
Factored receivables payable       1,077    
Current maturities of long-term debt, net 4,435          
Warrant liability 1,614          
Total current liabilities 26,463       19,833    
Long-term debt 3,762       910    
Long-term debt – related party 195       195    
Deferred tax liability 537       241    
Deferred revenue 2,678       3,764    
Deferred rent 180       83    
Total liabilities 33,815       25,026    
Commitments and contingencies      
Stockholders’ equity (deficit)      
Common stock, $0.0001 par value 6       4    
Additional paid-in capital 144,156       128,008    
Accumulated other comprehensive loss (338 )     (382 )  
Accumulated deficit (145,803 )     (123,604 )  
Total stockholders’ equity (deficit) (1,979 )     4,026    
Total liabilities and stockholders’ equity (deficit) 31,836       29,052    



Consolidated Statements of Operations and Comprehensive Income (Loss)

(In thousands, except per share information)

  Year Ended December 31,
  2020   2019
Net revenues $ 10,001       $ 19,150    
Cost of revenues 3,357       9,020    
Gross profit 6,644       10,130    
Operating expenses:      
Sales and marketing 1,653       2,706    
General and administrative 15,361       15,403    
Research and development 2,628       4,333    
Legal Settlement 4,500          
Total operating expenses 24,142       22,442    
Operating loss (17,498 )     (12,312 )  
Other income (expense):      
Interest expense (3,413 )     (581 )  
Loss on extinguishment of debt (2,158 )        
Fair value adjustment for warrant liabilities 872          
Other income       27    
Total other expense (4,699 )     (554 )  
Loss before taxes (22,197 )     (12,866 )  
Income tax (provision) benefit (2 )     (5 )  
Net loss (22,199 )     (12,871 )  
Cumulative translation adjustment 44       36    
Comprehensive loss $ (22,155 )     $ (12,835 )  
       
Loss per share, basic and diluted $ (0.50 )     $ (0.35 )  
       
Weighted-average common shares used to compute loss per share, basic and diluted 44,269       36,879    



Consolidated Statements of Cash Flows

(In thousands)

  Year Ended December 31,
  2020   2019
Operating activities      
Net loss $ (22,199 )     $ (12,871 )  
Adjustments to reconcile net loss to net cash provided by operating activities:      
Depreciation 11       59    
Amortization of acquired intangibles 142       268    
Amortization of debt discount and deferred financing costs 2,185          
Gain on change in fair value of warrants (872 )        
Loss on sale of digital currencies       4    
Loss on extinguishment of debt 2,158          
Non-cash interest expense 55          
Bad debt (recovery) expense 205       114    
Settlement of accounts payable (453 )        
Stock-based compensation 4,492       1,784    
Deferred income taxes          
Changes in operating assets and liabilities:      
Accounts receivable 796       1,817    
Prepaid expenses and other assets 65       184    
Accounts payable 427       740    
Accrued expenses 1,064       1,133    
Accrued legal settlement 3,000          
Deferred revenue (2,049 )     581    
Net cash used by operating activities (10,973 )     (6,187 )  
       
Investing activities      
Proceeds received from sale of digital currencies       88    
Capital expenditures       (18 )  
Net cash provided by investing activities       70    
       
Financing activities      
Proceeds from borrowings, net of issuance costs 14,815       1,105    
Proceeds from related party bridge loans 560          
Payments on convertible notes (8,418 )        
Payments on related party notes (560 )        
Proceeds from PhunCoin deposits       212    
Net repayments on factoring agreement (1,077 )     (1,357 )  
Proceeds from sales of common stock, net of issuance costs 9,177          
Proceeds from warrant exercises       6,092    
Proceeds from exercise of stock options 99       287    
Series A convertible preferred stock redemptions and dividend payments       (6,240 )  
Net cash provided for financing activities 14,596       99    
       
Effect of exchange rate on cash and restricted cash 46       36    
Net increase (decrease) in cash and restricted cash 3,669       (5,982 )  
Cash and restricted cash at the beginning of the period 362       6,344    
Cash and restricted cash at the end of the period $ 4,031       $ 362    
       
Supplemental disclosure of cash flow information      
Interest paid $ 1,251       $ 603    

  Year Ended December 31,
  2020   2019
Supplemental disclosure of non-cash information      
Issuance of common stock for payment of legal, earned bonus and board of director fees $ 1,283       $ 562    
Issuance of common stock upon partial conversions of Senior Convertible Note $ 2,266       $    
Reacquisition of equity component of Senior Convertible Note $ (1,388 )     $    
Equity classified cash conversion feature of Senior Convertible Note $ 219       $    
Waiver of sponsor promissory note $       $ 1,993    

Non-GAAP Financial Measures and Reconciliation

Adjusted EBITDA should be considered in addition to, not as a substitute for, or superior to, financial measures calculated in accordance with Generally Accepted Accounting Principles in the United States (“GAAP”). It is not a measurement of our financial performance under GAAP and should not be considered as an alternative to net income (loss), as applicable, or any other performance measures derived in accordance with GAAP and may not be comparable to other similarly titled measures of other businesses. Adjusted EBITDA has limitations as an analytical tool and should not be considered in isolation or as a substitute for analysis of our operating results as reported under GAAP. Some of these limitations include: (i) Non-cash compensation is and will remain a key element of our overall long-term incentive compensation package, although we exclude it as an expense when evaluating its ongoing operating performance for a particular period, (ii) Adjusted EBITDA does not reflect the impact of certain charges resulting from matters we consider not to be indicative of ongoing operations, and (iii) other companies in our industry may calculate Adjusted EBITDA differently than we do, limiting their usefulness as comparative measures.

We compensate for these limitations to Adjusted EBITDA by relying primarily on its GAAP results and using Adjusted EBITDA only for supplemental purposes. Adjusted EBITDA includes adjustments for items that may not occur in future periods. However, we believe these adjustments are appropriate because the amounts recognized can vary significantly from period to period, do not directly relate to the ongoing operations of our business and complicate comparisons of our internal operating results and operating results of other peer companies over time. Each of the normal recurring adjustments and other adjustments described in this paragraph help management with a measure of our operating performance over time by removing items that are not related to day-to-day operations or are non-cash expenses.

Reconciliation of GAAP to Non-GAAP Financial Measures

(In thousands)

  Year Ended December 31,
  2020   2019
Net loss $ (22,199 )     $ (12,871 )  
Add back:  Depreciation and amortization 153       328    
Add back:  Interest expense 3,413       581    
Add back/less:  Income tax (expense) benefit 2       5    
EBITDA (18,631 )     (11,957 )  
Add Back: Stock-based compensation 4,492       1,784    
Add Back: Legal settlement 4,500          
Add Back: Loss on extinguishment of debt 2,158          
Less: Fair value adjustment for warrant liabilities (872 )        
Adjusted EBITDA $ (8,353 )     $ (10,173 )  



Supplemental Information

($ In thousands)

  Year Ended December 31,   Change
  2020   2019   Amount   %
Net Revenue          
Platform subscriptions and services $ 9,108     $ 17,243     $ (8,135 )     (47.2 ) %
Application transaction 893     1,907     (1,014 )     (53.2 ) %
Total revenue $ 10,001     $ 19,150     $ (9,149 )     (47.8 ) %
Platform subscriptions and services as a percentage of total revenue 91.1 %   90.0 %        
Application transactions as a percentage of total revenue 8.9 %   10.0 %        

 



Vivos Therapeutics Reports Fourth Quarter and Full Year 2020 Financial Results and Operational Update

Full Year Revenue Increase of 15%

Management to Host Conference Call Today at 5:00 pm ET

HIGHLANDS RANCH, Colo., March 25, 2021 (GLOBE NEWSWIRE) — Vivos Therapeutics, Inc. (“Vivos” or “the Company”) (NASDAQ: VVOS), a medical technology company focused on developing and commercializing innovative treatments for patients suffering from sleep-disordered breathing, including mild-to-moderate obstructive sleep apnea (OSA), today reported financial results for the fourth quarter and full year ended December 31, 2020.

Financial and Operating Highlights:

  • Revenue was $3.3 million for the fourth quarter of 2020 and increased 15% to $13.1 million for the full year 2020, compared to $3.1 million and $11.4 million for the fourth quarter and full year 2019, respectively;
  • Gross profit was $2.7 million for the fourth quarter of 2020 and $10.4 million for the full year 2020, compared to gross profit of $2.2 million for the fourth quarter of 2019 and gross profit of $8.7 million for the full year 2019;
  • Gross margin was 81% for the fourth quarter of 2020 and 80% for the full year 2020, compared to 72% and 76% for the fourth quarter and full year 2019, respectively;
  • General and administrative expenses were $4.6 million for the fourth quarter of 2020 and $16.1 million for the full year 2020, compared to $4.1 million and $16.2 million for the fourth quarter and full year 2019, respectively;
  • Net loss was $6.2 million for the fourth quarter of 2020 and $12.1 million for the full year 2020, compared to $2.6 million for the fourth quarter of 2019 and $10.8 million for the full year 2019;
    • The $1.3 million additional loss in 2020 was primarily due to a non-cash settlement expense of $3.3 million offset by $1.8 million higher gross profit in 2020
  • Cash and cash equivalents were $18.2 million at December 31, 2020;
  • During 2020, Vivos surpassed 15,000 total cases treated with the Vivos System;
  • In December 2020, Vivos completed its initial public offering for net proceeds of approximately $21.6 million, after deducting underwriter discounts and commissions and offering expenses payable by Vivos;
  • Subsequent to year end:
    • Announced the commercial launch of AireO2, a new patient management software technology;
    • In February, submitted FDA 510(k) application for the Vivos mmRNA oral appliance® with indications to treat mild-to-moderate OSA;
    • Also in February, launched VivoScore™, powered by SleepImage®, a comprehensive home sleep test (HST); and
    • In March, opened the first Pneusomnia center, a clinician-owned, integrated medical-dental sleep center featuring the Vivos System.

“Successfully introducing a disruptive technology like ours takes a passionate mission-driven team, sufficient capital resources, and a little time to execute. Last December, we took a huge step forward with the completion of our IPO which provided the financial resources to execute our go-to-market strategy. Despite a global pandemic that closed dental offices across the U.S. and Canada for extended periods of time, our company still produced strong 2020 revenue results. Our positive financial performance reflects the continued growth of dentists enrolling in our Vivos Integrated Practice (VIP) program coupled with substantially higher appliance sales volume,” said Kirk Huntsman, Vivos Chairman and CEO. “We continue to see a gradual but accelerating recovery from office closures caused by the COVID 19 pandemic with increasing adoption of the Vivos System and related services as more dentists and healthcare providers learn about the compelling advantages of our technology. We also continue to increase awareness of our products and services through our marketing initiatives and our Medical Integration Division that creates strategic alliances within the medical and dental communities. In the near term, we will focus on levering our new VivoScore HST diagnostic product that we believe will assist VIPs in screening and treating more patients with our Vivos System. As we announced a few weeks ago, our VivoScore pilot test demonstrated the potential for 50% of patients who test positive for OSA to enter into Vivos System treatment.”

Huntsman added, “We remain fiercely committed to establishing revenue opportunities from complimentary technologies and services.”

Further information on Vivos’ financial results is included on the attached condensed consolidated balance sheets and statements of operations, and additional explanations of Vivos’ financial performance are provided in the Company’s Annual Report on Form 10-K for the twelve months ended December 31, 2020, which will be filed with the Securities and Exchange Commission (“SEC”). The full 10-K report will be available on the SEC Filings section of the Investor Relations section of Vivos’ website at https://vivoslife.com/investor-relations/.

Business Updates

In December 2020, the Company completed its initial public offering by issuing 4,025,000 common shares at a price of $6.00 per share, for net proceeds of approximately $21.6 million, after deducting underwriter discounts and commissions and offering expenses payable by the Company.

In January 2021, Vivos commercially launched AireO2, a new patient management software technology that will enable healthcare professionals to more effectively diagnose, treat and monitor patients with OSA and its related conditions. Developed in collaboration with Lyon Dental, AireO2 contains features that enhance healthcare professionals’ billing services and more, including practice management systems.

Later in January, the Company established a Clinical Advisory Board to further drive adoption and growth of its next-generation treatments for OSA. Members of Vivos’ Clinical Advisory Board include internationally recognized medical and dental industry veterans, who will work closely with management to drive further commercial success.

In early February 2021, Vivos submitted a 510(k) Class II application to the U.S. Food and Drug Administration (FDA) for its mmRNA oral appliance® with indications to treat mild-to-moderate OSA, sleep-disordered breathing and snoring in adults. Vivos’ mmRNA oral appliance® (modified mandibular Repositioning Nighttime Appliance) is a new version of the Company’s existing mRNA appliance®, which is an FDA-cleared Class II oral appliance. Assuming the mmRNA’s 510(k) Class II approval, Vivos expects to submit an application to a PDAC (Pricing, Data Analysis and Coding) contractor for the mmRNA to be added to the Centers for Medicare and Medicaid Services’ list of approved sleep apnea appliances. The process is expected to take approximately three to six months in total, although no assurances can be given as to the timing and outcome of the FDA’s review of this application.

Later in February, the Company launched VivoScore™, powered by SleepImage®. VivoScore is a comprehensive HST that utilizes proprietary cardiopulmonary coupling technology developed by MyCardio LLC (“SleepImage”). VivoScore consists of a single-sensor ring recorder that works with a mobile phone application and proprietary cloud-based algorithms to evaluate sleep quality and clinically diagnose sleep apnea. The Company anticipates increased revenue from VivoScore due to an expected increase in total patients tested and a corresponding increase in patient enrollment in Vivos System treatment. In arriving at that conclusion, the Company is relying on the results of a recently conducted informal pilot study with 12 independent Vivos-trained dentists, who performed 938 sleep-tests over a three-month period using VivoScore, and other Vivos provider feedback, which may or may not prove reliable on a broader scale.

In February 2021, Vivos (through its Medical Integration Division) opened the first Pneusomnia center, a clinician-owned, integrated medical-dental sleep center featuring the Vivos System. This first Pneusomnia center is located in Del Mar, Calif., and is owned and operated by a diverse group of local physicians led by Dr. Mimi Guarneri, cardiologist, founder and president of The Academy of Integrative Health and Medicine and an award-winning physician and researcher. The Company launched its Medical Integration Division in 2020 to foster an environment where more medical doctors could work directly with dentists (including dentists who participate in the VIP program) for treating sleep disorders in patients. Additionally, new Pneusomnia centers are currently being developed in Colorado, California, New Jersey and Nevada.

Conference Call

The Company will conduct a conference call today, March 25, 2021 at 5:00 p.m. (Eastern Time) to review the results as well as provide an overview of the Company’s recent milestones and growth strategy.

To access the conference call, please dial (877) 451-6152, or for international callers, (201) 389-0879. A replay will be available shortly after the call and can be accessed by dialing (844) 512-2921, or for international callers, (412) 317-6671. The passcode for the live call and the replay is 13717735. The replay will be available until April 8, 2021.

A live webcast of the conference call can be accessed on Vivos’ website at https://vivoslife.com/investor-relations/. An online archive of the webcast will be available on the Company’s website for 30 days following the call.

About Vivos Therapeutics, Inc.

Vivos Therapeutics Inc. (NASDAQ: VVOS) is a medical technology company focused on developing and commercializing innovative treatments for adult patients suffering from sleep-disordered breathing, including obstructive sleep apnea (OSA). The Vivos treatment for mild-to-moderate OSA involves customized oral appliances and protocols called the Vivos System. Vivos believes that its Vivos System oral appliance technology represents the first clinically effective non-surgical, non-invasive, non-pharmaceutical and cost-effective solution for people with mild-to-moderate OSA. Vivos oral appliances have proven effective in over 15,000 patients treated worldwide by more than 1,200 trained dentists. Combining technologies and protocols that alter the size, shape and position of the tissues of a patient’s upper airway, the Vivos System opens airway space and significantly reduce symptoms and conditions associated with mild-to-moderate OSA. The Vivos System has been shown to significantly lower Apnea Hypopnea Index scores and improve other conditions associated with OSA. The Vivos Integrated Practice (VIP) program offers dentists training and other value-added services in connection with using the Vivos System.

For more information, visit www.vivoslife.com.

Cautionary Note Regarding Forward-Looking Statements

This press release, the conference call referred to herein, and the statements of the Company’s management made in connection therewith contain “forward-looking statements” (as defined in Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended) concerning future events, particularly with respect to the public offering described herein. Words such as “may”, “should”, “expects”, “intends”, “plans”, “believes”, “anticipates”, “hopes”, “estimates” and variations of such words and similar expressions are intended to identify forward-looking statements. These statements involve known and unknown risks and are based upon a number of assumptions and estimates, which are inherently subject to significant uncertainties and contingencies, many of which are beyond the Company’s control. Actual results (including the actual results of the Company’s growth strategies, operational plans, results of operations and other matters to be addressed herein and on the conference call) may differ materially from those expressed or implied by such forward-looking statements. Factors that could cause actual results to differ materially include, but are not limited to, the risk factors described in Vivos’ filings with the Securities and Exchange Commission, including the Company’s Annual Report on Form 10-K for the year ended December 31, 2020. Vivos’ filings can be obtained free of charge on the SEC’s website at www.sec.gov. Except to the extent required by law, Vivos expressly disclaims any obligations or undertaking to release publicly any updates or revisions to any forward-looking statements contained herein to reflect any change in Vivos’ expectations with respect thereto or any change in events, conditions or circumstances on which any statement is based.

Investor Relations Contact:

Edward Loew
Investor Relations Officer
(602) 903-0095
[email protected]

Media Relations Contact:

Caitlin Kasunich / Jenny Robles
KCSA Strategic Communications
(212) 896-1241 / (212) 896-1231
[email protected] / [email protected]

VIVOS THERAPEUTICS, INC. AND SUBSIDIARIES
               
Consolidated Statements of Operations
    Year Ended
    December 31,
    2020     2019
             
Revenue              
Product revenue   $ 4,889,840       $ 4,349,623  
Service revenue     8,176,397         7,043,654  
Total revenue     13,066,237         11,393,277  
Cost of sales (exclusive of depreciation and amortization shown separately below)     2,653,429         2,736,034  
               
Gross profit     10,412,808         8,657,243  
               
Operating expenses              
General and administrative     16,090,049         16,172,505  
Sales and marketing     2,314,023         2,310,743  
Settlement     3,330,679          
Depreciation and amortization     717,865         751,228  
Total operating expenses     22,452,616         19,234,476  
               
Operating loss before interest expense and income taxes     (12,039,808 )       (10,577,233 )
               
Interest expense     (96,681 )       (137,876 )
Loss on sale of business             (60,343 )
Interest income     79,612         21,133  
               
Loss before income taxes     (12,056,877 )       (10,754,319 )
Income tax expense              
               
Net loss     (12,056,877 )       (10,754,319 )
               
Warrant beneficial conversion feature expense     (3,597,585 )        
Preferred stock accretion     (2,333,333 )       (1,000,000 )
               
Net loss attributable to common stockholders   $ (17,987,795 )     $ (11,754,319 )
               
Net loss per share attributable to common stockholders (basic and diluted)   $ (1.40 )     $ (0.95 )
               
Weighted average number of shares of Common Stock outstanding (basic and diluted)     12,869,266         12,331,280  
               

VIVOS THERAPEUTICS, INC. AND SUBSIDIARIES
         
Consolidated Balance Sheets
    December 31,   December 31,
      2020       2019  
         
ASSETS        
         
         
Current assets        
Cash and cash equivalents   $ 18,205,668     $ 469,353  
Accounts receivable, net     1,430,890       871,290  
Current portion of note receivable     84,696       84,696  
Deferred offering costs           263,814  
Prepaid expenses and other current assets     673,061       295,002  
Total current assets     20,394,315       1,984,155  
         
Property and equipment, net     871,597       1,139,501  
Intangible assets, net     270,121       689,151  
Note receivable, net – related party     810,635       785,061  
Goodwill     2,671,434       2,671,434  
Deposits     309,367       282,235  
Total assets   $ 25,327,469     $ 7,551,537  
         
LIABILITIES AND STOCKHOLDER’S EQUITY        
Current liabilities        
Accounts payable   $ 781,364     $ 1,083,422  
Accounts payable – related party     1,500,000        
Accrued expenses     1,736,721       1,353,161  
Contract liability     2,937,992       2,947,565  
Current portion of long-term debt     866,972       3,709,535  
Total current liabilities     7,823,049       9,093,683  
         
Long-term debt     423,095        
Deferred rent     163,966       84,246  
Total liabilities     8,410,110       9,177,929  
         
Commitments and contingencies        
         
Convertible Redeemable Series A Preferred Stock – $0.0001 par value. 50,000,000 shares authorized, none and 730,000 shares issued and outstanding at December 31, 2020 and 2019, respectively           1,316,667  
         
Stockholders’ equity        
Preferred Stock        
Series B, nonvoting – $0.0001 par value, 1,200,000 authorized, none issued and outstanding at December 31, 2020 and 2019, respectively            
Common Stock        
Class A, voting – $0.0001 par value, 200,000,000 shares authorized, 18,209,452 and 12,444,165 issued and outstanding at December 31, 2020 and 2019, respectively     1,821       1,244  
Additional paid-in capital     52,250,266       20,333,548  
Accumulated deficit     (35,334,728 )     (23,277,851 )
Total stockholders’ equity     16,917,359       (2,943,059 )
Total liabilities and stockholders’ equity   $ 25,327,469     $ 7,551,537  
         



Relay Therapeutics Reports Fourth Quarter and Full Year 2020 Financial Results and Operational Highlights

Advanced two programs, RLY-1971 and RLY-4008, into clinical development, and on track to initiate IND enabling studies with PI3Kα mutant selective inhibitor in 2021

Entered into a global collaboration with Genentech for the development and commercialization of 
RLY-1971

Continued to advance three additional oncology preclinical programs and extended work outside of oncology into genetic diseases with two preclinical programs

$678.1 million in cash, cash equivalents and marketable securities at end of 2020, with the $75 million upfront payment received from Genentech in 2021, expected to fund operations into 2024

CAMBRIDGE, Mass., March 25, 2021 (GLOBE NEWSWIRE) — Relay Therapeutics, Inc. (Nasdaq: RLAY), a clinical-stage precision medicine company transforming the drug discovery process by combining leading edge experimental and computational technologies, today reported fourth quarter and full year 2020 financial results and operational highlights.

“2020 was a transformational year for Relay Therapeutics. We successfully advanced multiple programs into the clinic, evolved our platform, expanded our strong team and completed a successful IPO,” said Sanjiv Patel, M.D., president and chief executive officer. “While the last few years were spent validating our approach of combining leading edge experimental and computational techniques to create potentially life-saving therapies for patients, the next chapter will be about extending our platform leadership and delivering meaningful clinical results to support the success of our programs. 2021 will be a critical year of execution as we advance our mission of transforming drug discovery to address some of the most devastating diseases.”

2020 Corporate Highlights

  • Initiated first-in-human clinical studies for RLY-1971 (SHP2 inhibitor) and RLY-4008 (FGFR2 inhibitor)
  • Progressed PI3Kα mutant selective program into late lead optimization
  • Continued to advance three additional precision oncology programs through preclinical development
  • Expanded research efforts into genetic diseases with two preclinical programs
  • Strengthened the balance sheet with $460 million gross proceeds raised in an initial public offering
  • Announced a worldwide license and collaboration agreement with Genentech, Inc., a member of the Roche Group, for the development and commercialization of RLY-1971

2021 Anticipated Milestones

  • Present preclinical data for RLY-4008 at the American Association for Cancer Research (AACR) Annual Meeting 2021
  • Announce initial clinical data for RLY-4008 in the second half of 2021
  • Genentech to initiate RLY-1971 and GDC-6036 (KRAS G12C inhibitor) combination trial
  • Enter IND-enabling studies for PI3Kα mutant selective inhibitor and provide program update

Fourth Quarter and Full Year 2020 Financial Results

Cash, Cash Equivalents and Investments: As of December 31, 2020, cash, cash equivalents and investments totaled approximately $678.1 million, compared to $355.8 million as of December 31, 2019. The Company expects its current cash and cash equivalents, including the $75 million upfront payment received from Genentech in 2021, will be sufficient to fund its current operating plan into 2024.

R&D Expenses: Research and development expenses were $32.1 million for the fourth quarter of 2020, as compared to $22.4 million for the fourth quarter of 2019. This increase was primarily due to $7.4 million of increased employee related costs, including $5.7 million of additional share-based compensation expense, primarily due to increases in our stock price and increased headcount, and $2.3 million in increased clinical trial expenses. Research and development expenses were $99.9 million for the full year 2020, as compared to $70.3 million for the full year 2019.

G&A Expenses: General and administrative expenses were $15.5 million for the fourth quarter of 2020, as compared to $3.4 million for the fourth quarter of 2019. This increase was primarily due to $9.1 million of increased employee related costs, including $7.5 million of additional share-based compensation expense, primarily due to increases in our stock price and increased headcount, as well as $3.0 million of increased general expenses, primarily driven by public company related costs. General and administrative expenses were $38.6 million for the full year 2020, as compared to $13.7 million for the full year 2019.

Net Income/Loss: Net income was $35.3 million for the fourth quarter of 2020, as compared to a net loss of $23.9 million for the fourth quarter of 2019. Net loss was $52.4 million for the full year 2020, or a net loss per share of $5.40, as compared to a net loss of $75.3 million for the full year 2019, or a net loss per share of $21.82.

About Relay Therapeutics

Relay Therapeutics® (Nasdaq: RLAY) is a clinical-stage precision medicines company transforming the drug discovery process with the goal of bringing life-changing therapies to patients. Built on unparalleled insights into protein motion and how this dynamic behavior relates to protein function, Relay Therapeutics aims to effectively drug protein targets that have previously been intractable, with an initial focus on enhancing small molecule therapeutic discovery in targeted oncology. The Company’s Dynamo™ platform integrates an array of leading-edge experimental and computational approaches to provide a differentiated understanding of protein structure and motion to drug these targets. For more information, please visit www.relaytx.com or follow us on Twitter.

Cautionary Note Regarding Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, as amended, including, without limitation, implied and express statements regarding the Company’s strategy, business plans and focus; the progress and timing of updates on the clinical development of the programs across the Company’s portfolio, including the timing of the Company’s first expected data readout for RLY-4008, ability to enter IND-enabling studies for its PI3Kα mutant selective inhibitor program, expected therapeutic benefits of its programs, presentation of additional data at upcoming scientific conferences and other preclinical data in 2021, ability to optimize the impact of collaborations on the Company’s programs, including but not limited to the Company’s collaboration with Genentech and the expected initiation of the RLY-1971 and GDC-6036 (KRAS G12C inhibitor) combination trial, expectations regarding the Company’s use of capital, expenses, future accumulated deficit and other financial results during 2021 and in the future, and the Company’s ability to fund operations through at least 2024. The words “may,” “might,” “will,” “could,” “would,” “should,” “expect,” “plan,” “anticipate,” “intend,” “believe,” “expect,” “estimate,” “seek,” “predict,” “future,” “project,” “potential,” “continue,” “target” and similar words or expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words.

Any forward-looking statements in this press release are based on management’s current expectations and beliefs and are subject to a number of risks, uncertainties and important factors that may cause actual events or results to differ materially from those expressed or implied by any forward-looking statements contained in this press release, including, without limitation, risks associated with: the impact of COVID-19 on countries or regions in which we have operations or do business, as well as on the timing and anticipated results of our clinical trials, strategy and future operations; the delay of any current or planned clinical trials or the development of the Company’s drug candidates; the risk that the results of our clinical trials may not be predictive of future results in connection with future clinical trials; the Company’s ability to successfully demonstrate the safety and efficacy of its drug candidates; the timing and outcome of the Company’s planned interactions with regulatory authorities; and obtaining, maintaining and protecting its intellectual property.  These and other risks and uncertainties are described in greater detail in the section entitled “Risk Factors” in Relay Therapeutics’ Annual Report on Form 10-K expected to be filed on or about March 25, 2021, its most recent Quarterly Report on Form 10-Q as well as any subsequent filings with the Securities and Exchange Commission. In addition, any forward-looking statements represent Relay Therapeutics’ views only as of today and should not be relied upon as representing its views as of any subsequent date. Relay Therapeutics explicitly disclaims any obligation to update any forward-looking statements. No representations or warranties (expressed or implied) are made about the accuracy of any such forward-looking statements.

Contact:

Pete Rahmer
Senior Vice President, Corporate Affairs and Investor Relations
617-322-0715
[email protected]

Media:
Dan Budwick
1AB
973-271-6085
[email protected]

 
Relay Therapeutics, Inc.
Consolidated Statements of Operations and Comprehensive Loss
(In thousands, except share and per share data)
 
    Year Ended

December 31,
    2020     2019  
Revenue:                
License revenue   $ 82,654     $  
Total revenue     82,654        
Operating expenses:                
Research and development expenses     99,862       70,306  
General and administrative expenses     38,588       13,742  
Total operating expenses     138,450       84,048  
Loss from operations     (55,796 )     (84,048 )
Other income (expense):                
Interest income     3,400       8,801  
Other expense     (16 )     (58 )
Total other income (expense), net     3,384       8,743  
Net loss   $ (52,412 )   $ (75,305 )
Deemed dividend resulting from extinguishment upon
   modification of series C preferred stock
    (177,789 )      
Net loss attributable to common stockholders   $ (230,201 )   $ (75,305 )
Net loss attributable to common stockholders per share,
   basic and diluted
  $ (5.40 )   $ (21.82 )
Weighted average shares of common stock, basic and
   diluted
    42,619,582       3,450,500  
Other comprehensive income (loss):                
Unrealized holding gain (loss)     (261 )     325  
Total other comprehensive income (loss)     (261 )     325  
Total comprehensive loss   $ (52,673 )   $ (74,980 )

 
Relay Therapeutics, Inc.
Selected Condensed Consolidated Balance Sheet Data
(In thousands)
 
    December 31,

2020
    December 31,

2019
 
Cash, cash equivalents and investments   $ 678,061     $ 355,816  
Working capital (1)     756,468       348,550  
Total assets     799,829       393,068  
Total liabilities     36,536       35,725  
Convertible preferred stock           537,781  
Total stockholders’ equity (deficit)     763,293       (180,438 )
Restricted cash     878       878  

(1)   Working capital is defined as current assets less current liabilities.