Apollo Commercial Real Estate Finance, Inc. to Present at Citi Global Property CEO Conference

NEW YORK, March 04, 2021 (GLOBE NEWSWIRE) — Apollo Commercial Real Estate Finance, Inc. (the “Company” or “ARI”) (NYSE:ARI) today announced Stuart Rothstein, the Company’s Chief Executive Officer, is scheduled to present at the Citi Global Property CEO Conference on March 9, 2021. The presentation is scheduled to begin at 8:15 am ET.

The presentation and question and answer periods will be broadcast live over the Internet and can be accessed by all interested parties through the Company’s website at www.apolloreit.com in the Stockholders section. There will be a replay available following the presentation which will remain on the Company’s website for thirty days.

About Apollo Commercial Real Estate Finance, Inc.

Apollo Commercial Real Estate Finance, Inc. (NYSE: ARI) is a real estate investment trust that primarily originates, acquires, invests in and manages performing commercial first mortgage loans, subordinate financings and other commercial real estate-related debt investments. The Company is externally managed and advised by ACREFI Management, LLC, a Delaware limited liability company and an indirect subsidiary of Apollo Global Management, Inc., a leading global alternative investment manager with approximately $455 billion of assets under management at December 31, 2020.

Additional information can be found on the Company’s website at www.apolloreit.com.

Forward-Looking Statements

Certain statements contained in this press release constitute forward-looking statements as such term is defined in Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended, and such statements are intended to be covered by the safe harbor provided by the same. Forward-looking statements are subject to substantial risks and uncertainties, many of which are difficult to predict and are generally beyond the Company’s control. These forward-looking statements include information about possible or assumed future results of the Company’s business, financial condition, liquidity, results of operations, plans and objectives. When used in this release, the words believe, expect, anticipate, estimate, plan, continue, intend, should, may or similar expressions, are intended to identify forward-looking statements. Statements regarding the following subjects, among others, may be forward-looking: macro- and micro-economic impact of the COVID-19 pandemic; the severity and duration of the COVID-19 pandemic; actions taken by governmental authorities to contain the COVID-19 pandemic or treat its impact; the impact of the COVID-19 pandemic on the Company’s financial condition, results of operations, liquidity and capital resources; market trends in the Company’s industry, interest rates, real estate values, the debt securities markets or the general economy; the timing and amounts of expected future fundings of unfunded commitments; the return on equity; the yield on investments; the ability to borrow to finance assets; the Company’s ability to deploy the proceeds of its capital raises or acquire its target assets; and risks associated with investing in real estate assets, including changes in business conditions and the general economy. For a further list and description of such risks and uncertainties, see the reports filed by the Company with the Securities and Exchange Commission. The forward-looking statements, and other risks, uncertainties and factors are based on the Company’s beliefs, assumptions and expectations of its future performance, taking into account all information currently available to the Company. Forward-looking statements are not predictions of future events. The Company disclaims any intention or obligation 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: Hilary Ginsberg
  Investor Relations
  (212) 822-0767



BrewBilt Orders for 1st Quarter Exceed $3.1M and $125M Strategic Partnership With BrewBilt Brewing Company

SACRAMENTO, CA, March 04, 2021 (GLOBE NEWSWIRE) — via NewMediaWire — Today BrewBilt Manufacturing Inc. (the “Company”) (OTCPINK: BBRW), announces 1st quarter revenue of $3.1M and our newest strategic partnership with BrewBilt Brewing Company.  

Jef Lewis, Chairman and CEO, stated, “Today is a historical event with BrewBilt Manufacturing. The company reports $3.1M in 1st quarter revenue, with $17M in pending orders, and growing. We have opened markets in Korea, Finland, and various parts of North America. We have millions of following globally, and the company continues to snow-ball its products and growth across the craft brew world of beer drinkers.”

Mr. Lewis further stated, “More important is that we have a strategic partnership with BrewBilt Brewing Company (Florida Corporation). This company is a reorganization of another public company, symbols SIML, and will be filing the PRE14C this month as a part of reorganization to build the brewery. SIML has purchased the facility, and the brewing facility will be licensed and in operation by summer-2021. The strategic partnership will allow revenue capture for customers who want to build a brewery and customers seeking a contract brewery to make craft beer. Both companies will cross pollinate marketing and sales. Projected beer sales are $25M-$125M over the next 36 months. Projected revenue for building brewery systems is projected to be $250M over the next 48 months.”

The company continues to repurchase stock up to $5M by 12/31/2021. Further, as a part of the SEC changes with Rule-144, the company has filed the Registration-A to avoid any toxic convertible note funding and to be compliant with its Broker-Dealer with any future funding needs under the Registration-A Offering. The company will self-fund future operations.

Watch Video Success Stories:

Who is Jef Lewis: https://www.brewbilt.com/meet-the-chairman

Visit Our Breweries: https://www.youtube.com/watch?reload=9&v=eAtMrDj7PYA&feature=youtu.be

ABOUT BREWBILT:  (www.brewbilt.com)

Located in the Sierra Foothills of Northern California, BrewBilt is one of the only California companies that custom designs, hand crafts, and integrates processing, fermentation and distillation processing systems for the craft beer, cannabis and hemp industries using “Best in Class” American made components integrated with stainless steel processing vessels using only American made steel. Founded in 2014, the company began in a backyard shop by Jef Lewis with a vision of creating a profitable company in “Rural America”. BrewBilt has built a solid foundation by having strong relationships with local suppliers of raw materials, equipment and services in California, an aggressive referral network of satisfied customers nationwide, and an Advisory Board consisting of successful business leaders that provide valuable product feedback and business expertise to management. The craft brewing & spirits industries continue to grow worldwide. California is where craft brewing began and now has over 900 operating breweries – being centrally located in this booming market was a large draw for BrewBilt to locate its manufacturing facility in the Sierra foothills. All BrewBilt products are designed and fabricated as “food grade” quality which enables the company to build vessels for food & beverage processing. More important, the company has been building systems that are pharmaceutical grade for clients involved in distillation for the cannabis and hemp industries over the past 36 months, thus making the revenue potential much greater. 

FORWARD LOOKING STATEMENTS This document contains forward-looking statements.  Forward-looking statements provide current expectations or forecasts of future events and are not guarantees of future performance, nor should they be relied upon as representing management’s views as of any subsequent date.  The forward-looking statements are based on management’s expectations and are subject to a number of risks and uncertainties.  Although management believes that the expectations reflected in such forward-looking statements are reasonable, actual results may differ materially from those expressed or implied in such statements.  Risks and uncertainties that could cause actual results to differ materially include, without limitation, the Corporation’s ability to effectively execute its business plans; changes in general economic and financial market conditions; changes in interest rates; changes in the competitive environment; continuing consolidation in the financial services industry; new litigation or changes in existing litigation; losses, customer bankruptcy, claims and assessments; changes in banking regulations or other regulatory or legislative requirements affecting the Corporation’s business; and changes in accounting policies or procedures as may be required by the Financial Accounting Standards Board or other regulatory agencies.  Management may elect to update forward-looking statements at some future point; however, it specifically disclaims any obligation to do so.

Contact:

Jef Lewis, Chairman and CEO 

BrewBilt Manufacturing Inc. –  BBRW 

Call or Text: 530-802-5023

[email protected]

Source: BrewBilt Manufacturing Inc.



Oncology Pharma Moves to Fund Lead Drug Formulation & IND-Enabling Studies

San Francisco, CA, March 04, 2021 (GLOBE NEWSWIRE) — via NewMediaWire — Oncology Pharma Inc. (OTC: ONPH) is pleased to announce initiation of formal drug development and preclinical planning for its lead drug product, based upon proprietary nanoemulsion technology licensed from NanoSmart Pharmaceuticals.  Oncology Pharma will be providing the initial funds to develop and evaluate a dactinomycin nanoemulsion drug product.  A version of this product originally received FDA Orphan Drug Designation in 2015.

Oncology Pharma has secured access to a broad range of proprietary intellectual property with the potential to make novel drug products to treat cancer that are both safer and more effective than the original drug(s) currently in the market.  Oncology Pharma has initiated discussions with NanoSmart on near-term goals including analytical method validation and drug product characterization.  Once complete, formal preclinical safety and veterinary clinical studies will be pursued. Veterinary drug development will serve a current and growing need for better treatment options.  Data from this project may also be applied towards future regulatory approval to initial human clinical studies for the same drug formulation.

ABOUT ONCOLOGY PHARMA, INC.

ONCOLOGY PHARMA, INC. (OTCPK: ONPH) (the “Company”) is currently engaging in research and development of therapeutics for oncology and prides itself for having a world-class Advisory Board that keeps the Company in the forefront of developing technologies in cancer research, biotechnology, and healthcare.

ABOUT NANOSMART PHARMACEUTICALS, INC.

NanoSmart® Pharmaceuticals is a privately-held California corporation that is developing nanoparticle drug delivery platforms that utilize anti-nuclear antibody (ANA) to target existing drug therapies to areas of necrosis present in virtually all solid cancer tumors.

FORWARD LOOKING STATEMENTS

Certain of the matters discussed in this announcement contain forward-looking statements that involve material risks to and uncertainties in the Company’s business that may cause actual results to differ materially from those anticipated by the statements made herein. Such risks and uncertainties include risks related to licensing arrangements and joint ventures, including the need to negotiate the definitive agreements for the relationships; possible failure to realize anticipated benefits of business relationships; and, costs of providing funding to these business relationships. Other risks and uncertainties relating to the Company include, among other things, current negative operating cash flows and a need for additional funding to finance our operating plan; the terms of any further financing, which may be highly dilutive and may include onerous terms; unexpected costs and operating deficits, and lower than expected sales and revenues; uncertain willingness and ability of customers to adopt new technologies and other factors that may affect further market acceptance; adverse economic conditions; adverse results of any legal proceedings; the volatility of our operating results and financial condition; inability to attract or retain qualified senior management personnel, including sales and marketing personnel; our ability to establish and maintain the proprietary nature of our technology through the patent process, as well as our ability to possibly license from others patents and patent applications necessary to develop products; the Company’s ability to implement its long range business plan for various applications of its technology; the Company’s ability to enter into agreements with any necessary marketing and/or distribution partners and with any strategic or joint venture partners; the impact of competition; the obtaining and maintenance of any necessary regulatory clearances applicable to applications of the Company’s technology; management of growth; and, other risks and uncertainties. This is not a solicitation to buy or sell securities and does not purport to be an analysis of the Company’s financial position.

CONTACTS:

For additional Information, please contact the Oncology Pharma at:

One Sansome Street, Suite 3500

San Francisco, CA 94104

Phone: 415-869-1038 

Fax: 415-946-8801 

website: www.oncology-pharma.com

email: [email protected]



X4 Pharmaceuticals Reports Fourth Quarter and Full Year 2020 Financial Results and Provides Corporate Update


2021 expected to be a year of key value-driving catalysts as company advances multiple 


clinical programs with lead candidate mavorixafor


Company anticipates completing full enrollment in WHIM Phase 3 trial in 2021 and presenting clinical data from the ongoing Phase 1b Waldenström’s trial throughout the year


Conference call today at 8:30 a.m. ET

BOSTON, March 04, 2021 (GLOBE NEWSWIRE) — X4 Pharmaceuticals, Inc. (Nasdaq: XFOR), a leader in the discovery and development of novel therapies targeting diseases resulting from dysfunction of the CXCR4 pathway, today reported financial results for the fourth quarter and full year ended December 31, 2020. The company also provided an update on its lead product candidate, mavorixafor, a novel small molecule currently being evaluated in a Phase 3 clinical trial (4WHIM) for patients with WHIM (warts, hypogammaglobulinemia, infections, and myelokathexis) syndrome and in two Phase 1b trials for patients with Waldenström’s macroglobulinemia (Waldenström’s) and Severe Congenital Neutropenia (SCN), respectively.

“As many companies did, we encountered a number of unexpected challenges in 2020, most notably the COVID-19 pandemic. However, I could not be prouder of our accomplishments, as we remained steadfast in our commitment to advance our lead candidate, mavorixafor, in a number of rare disease indications,” said Paula Ragan, Ph.D., President and Chief Executive Officer of X4 Pharmaceuticals. “We believe that we have much to look forward to this year, as we have overcome these obstacles, have made significant progress in advancing our clinical and research programs, and assembled an exceptional team to execute on our 2021 goals and beyond.

“On the clinical front, we continue to expect top-line data from our Phase 3 WHIM trial in 2022 and, as our Phase 1b Waldenström’s trial is progressing well, we continue to expect initial data from that study in the first half of 2021, with a more fulsome dataset expected towards the end of 2021. We also anticipate initial data from our SCN Phase 1b trial in 2021.”


Recent Highlights

  • Received Fast Track and Rare Pediatric Designations (RPD) from the FDA for Mavorixafor for the treatment of WHIM Syndrome: These FDA designations further recognize WHIM as a serious condition with a clear unmet need in both adult and pediatric populations.

    • Through the Fast Track program, X4 will be eligible for more frequent meetings with the FDA to discuss the drug’s development plan, protocols and clinical data that would support mavorixafor’s potential approval for WHIM.
    • Under the RPD program, a sponsor who receives an approval for a drug for a “rare pediatric disease” and a Fast Track designation may qualify for a voucher that can be redeemed to receive a priority review by the FDA for any subsequent marketing application for a different product. Such a voucher is transferable and may be sold.
    • Mavorixafor was previously granted Breakthrough Therapy Designation by the FDA, as well as Orphan Drug status by the FDA and the European Commission for the treatment of WHIM syndrome.
  • Strengthened Leadership Team: During the Fourth Quarter of 2020:

    • Diego Cadavid, M.D., joined as Chief Medical Officer, bringing more than 20 years of industry experience and having led multiple programs through all phases of clinical development, including small molecules and biologics for the treatment of rare and immunological diseases.
    • Art Taveras, Ph.D., joined as Chief Scientific Officer with more than 30 years of experience leading small molecule research and development programs focused on cancer, dysregulated immune disorders, neurodegeneration, and metabolic diseases.
    • Alison Lawton was appointed to the company’s Board of Directors, bringing more than 30 years of experience across a full spectrum of drug development and commercial roles and having previously served on X4’s corporate advisory board and as consulting Chief Operating Officer.


Fourth Quarter 2020 Financial Results

  • Cash, Cash Equivalents & Restricted Cash: X4 had $80.7 million in cash, cash equivalents and restricted cash as of December 31, 2020. X4 continues to expect that its cash and cash equivalents will fund company operations into 2022.
  • Research and Development Expenses were $12.3 million and $41.9 million for the fourth quarter and full year ended December 31, 2020, respectively, as compared to $7.1 million and $30.2 million for the comparable periods in 2019, respectively. R&D expenses include $0.6 million and $2.3 million of certain non-cash expenses for the fourth quarter and fully year ended December 31, 2020, respectively.
  • General and Administrative Expenses were $5.4 million and $20.9 million for the fourth quarter and full year ended December 31, 2020, respectively, as compared to $3.9 million and $17.6 million for the comparable periods in 2019, respectively. G&A expenses include $0.8 million and $3.1 million of certain non-cash expenses for the fourth quarter and full year ended December 31, 2020, respectively.
  • Net Loss: X4 reported net losses of $18.4 million and $62.1 million for the fourth quarter and full year ended December 31, 2020 as compared to net losses of $10.8 million and $52.8 million for the comparable periods in 2019, respectively. Net losses include $1.4 million and $5.4 million of certain non-cash expenses for the fourth quarter and full year ended December 31, 2020, respectively. Net losses in the full year of 2019 included a $3.9 million loss on the sale of non-financial assets.


Conference Call and Webcast


The Company will host a conference call and webcast today at 8:30 a.m. ET to discuss these financial results and business highlights. The conference call can be accessed by dialing (866) 721-7655 from the United States or (409) 216-0009 internationally, followed by the conference ID: 1053189. The live webcast can be accessed on the investor relations section of X4 Pharmaceuticals’ website at www.x4pharma.com. Following the completion of the call, a webcast replay of the conference call will be available on the website.

About X4 Pharmaceuticals

X4 Pharmaceuticals is a late-stage clinical biopharmaceutical company and a leader in the discovery and development of novel therapies for the treatment of diseases resulting from dysfunction of the CXCR4 pathway, with a focus on rare diseases and those with limited treatment options. The company’s lead candidate, mavorixafor, is a first-in-class, small molecule antagonist of chemokine receptor CXCR4 being developed as a once-daily oral therapy. X4 believes that inhibition of the CXCR4 receptor creates the potential for mavorixafor to provide therapeutic benefit across a wide variety of diseases, including primary immunodeficiencies and certain types of cancer. The efficacy and safety of mavorixafor, dosed once daily, is currently being evaluated in a global Phase 3 clinical trial in patients with WHIM syndrome, and in two Phase 1b clinical trials – in combination with ibrutinib in patients with Waldenström’s macroglobulinemia, and as monotherapy in patients with Severe Congenital Neutropenia. X4 is continuing to leverage its insights into CXCR4 biology at its corporate headquarters in Boston, Massachusetts and at its research facility in Vienna, Austria, and is discovering and developing additional product candidates. For more information, please visit www.x4pharma.com.

Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, as amended. These statements may be identified by the words “may,” “will,” “could,” “would,” “should,” “expect,” “plan,” “anticipate,” “intend,” “believe,” “estimate,” “predict,” “project,” “potential,” “continue,” “target,” or other similar terms or expressions that concern X4’s expectations, strategy, plans or intentions. Forward-looking statements include, without limitation, statements regarding the clinical development of mavorixafor and X4’s other product candidates or programs, the potential benefits resulting from Fast Track and Rare Pediatric Disease designations, and the company’s cash runway. Any forward-looking statements in this press release are based on management’s current expectations and beliefs. Actual events or results may differ materially from those expressed or implied by any forward-looking statements contained herein, including, without limitation, the risks and uncertainties described in the section entitled “Risk Factors” in X4’s Quarterly Report on Form 10-Q filed with the Securities and Exchange Commission (SEC) on November 5, 2020, and in other filings X4 makes with the SEC from time to time. X4 undertakes no obligation to update the information contained in this press release to reflect new events or circumstances, except as required by law.

(Tables Follow)



X4 PHARMACEUTICALS, INC.

CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS

(in thousands, except per share amounts)

(unaudited)

  Three Months Ended   Year Ended
  December 31,   December 31,
  2020   2019   2020   2019
License revenue $     $     $ 3,000     $  
Operating expenses:              
Research and development 12,298     7,065     41,932     30,163  
General and administrative 5,357     3,914     20,942     17,640  
Loss on transfer of non-financial assets     (104 )       3,900  
Total operating expenses 17,655     10,875     62,874     51,703  
Loss from operations (17,655 )   (10,875 )   (59,874 )   (51,703 )
Other income (expense), net (745 )   38     (2,109 )   (1,104 )
Loss before provision for income taxes (18,400 )   (10,837 )   (61,983 )   (52,807 )
Provision for income taxes         148      
Net loss (18,400 )   (10,837 )   (62,131 )   (52,807 )
Adjustments related to convertible preferred stock             (592 )
Net loss attributable to common stockholders $ (18,400 )   $ (10,837 )   $ (62,131 )   $ (53,399 )
Net loss per share attributable to common stockholders- basic and diluted $ (0.91 )   $ (0.66 )   $ (3.09 )   $ (4.63 )
Weighted average common shares outstanding-basic and diluted 20,174     16,466     20,077     11,530  





X4 PHARMACEUTICALS, INC.

CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS

(in thousands)

(unaudited)

  Year ended December 31,
  2020   2019
Net loss $ (62,131 )   $ (52,807 )
Adjustments to reconcile net loss to net cash used in operating activities 7,376      7,988   
Changes in operating assets and liabilities (4,063 )   (3,236 )
Net cash used in operating activities (58,818 )   (48,055 )
Net cash (used in) provided by investing activities (1,362 )   27,232   
Net cash provided by financing activities 12,394      140,661   
Impact of foreign exchange on cash, cash equivalents and restricted cash 402     (250 )
Net (decrease) increase in cash, cash equivalents and restricted cash (47,384 )   119,588   
Cash, cash equivalents and restricted cash at beginning of period 128,086      8,498   
Cash, cash equivalents and restricted cash at end of period $ 80,702      $ 128,086   





X4 PHARMACEUTICALS, INC.

CONSOLIDATED BALANCE SHEETS

(in thousands)

(unaudited)

  December 31, 2020   December 31, 2019
Current assets:      
Cash and cash equivalents $ 78,708     $ 126,184  
Research and development incentive receivable 917     1,998  
Prepaid expenses and other current assets 3,682     1,096  
Total current assets 83,307     129,278  
Property and equipment, net 1,237     403  
Goodwill 27,109     27,109  
Right-of-use assets 7,960     1,959  
Other assets 3,258     1,949  
Total assets $ 122,871     $ 160,698  
Current liabilities:      
Accounts payable $ 3,144     $ 2,088  
Accrued expenses 8,018     6,461  
Current portion of lease liability 786     898  
Total current liabilities 11,948     9,447  
Long-term debt, including accretion, net of discount 33,178     20,097  
Lease liabilities 4,484     1,918  
Other liabilities 462     16  
Total liabilities 50,072     31,478  
Total stockholders’ equity 72,799     129,220  
Total liabilities and stockholders’ equity $ 122,871     $ 160,698  


Contacts:

Daniel Ferry (Investors)

Managing Director
LifeSci Advisors
[email protected]
(617) 430-7576

Mónica Rouco Molina (Media)

Senior Account Executive
LifeSci Communications
[email protected]

 



Decibel Therapeutics to Present at the Barclays Global Healthcare Conference

BOSTON, March 04, 2021 (GLOBE NEWSWIRE) — Decibel Therapeutics (Nasdaq: DBTX), a clinical-stage biotechnology company dedicated to discovering and developing transformative treatments to restore and improve hearing and balance, announced today that Laurence Reid, Ph.D., Chief Executive Officer of Decibel, will present at the Barclays Global Healthcare Conference on Thursday, March 11, 2021 at 9:10 a.m. ET.

A live webcast of the presentation may be accessed by visiting the Investors section of the Decibel Therapeutics website at https://ir.decibeltx.com. An archived replay of the webcast will be available on the company’s website for approximately 90 days following the presentation.

About Decibel Therapeutics

Decibel Therapeutics is a clinical-stage biotechnology company dedicated to discovering and developing transformative treatments to restore and improve hearing and balance, one of the largest areas of unmet need in medicine. Decibel has built a proprietary platform that integrates single-cell genomics and bioinformatic analyses, precision gene therapy technologies and expertise in inner ear biology. Decibel is leveraging its platform to advance gene therapies designed to selectively replace genes for the treatment of congenital, monogenic hearing loss and to regenerate inner ear hair cells for the treatment of acquired hearing and balance disorders. Decibel’s pipeline, including its lead gene therapy program, DB-OTO, to treat congenital, monogenic hearing loss, is designed to deliver on our vision of a world in which the privileges of hearing and balance are available to all.

Investor Contact:

Julie Seidel
Stern Investor Relations, Inc.
[email protected]
212-362-1200

Media Contact:

Stephanie Simon
Ten Bridge Communications
[email protected]
617-581-9333



GridGain Offers New Training and Certification Programs for GridGain and Apache Ignite Architects and Developers

Programs offered for organizations and individuals provide fast track to in-memory computing platform expertise

FOSTER CITY, Calif., March 04, 2021 (GLOBE NEWSWIRE) — GridGain® Systems, provider of enterprise-grade in-memory computing solutions powered by the Apache® Ignite® distributed database, today announced GridGain Training, a new training and certification program for application architects, developers and system administrators who want to master GridGain and Apache Ignite. GridGain Training is the only training program that lets attendees learn about GridGain and Apache Ignite from the team that contributed Apache Ignite to the Apache Software Foundation. GridGain Training includes both free and low-cost programs for individuals and organizations. Training program attendees will receive badges and certificates so they can share their Apache Ignite proficiency with peers and prospective employers.

“The pace of adoption of GridGain and Apache Ignite continues to soar, increasing the demand for expertise required to deploy these solutions,” said Lalit Ahuja, Vice President of Solutions and Services at GridGain. “GridGain Training sessions are conducted by GridGain engineers and solution architects with deep technical expertise and real-world experience solving customer problems. During the sessions, attendees will use the actual products, and learn how to unlock the full potential of the Ignite platform and the advanced capabilities of GridGain. Whether for an individual who wants to become a GridGain certified expert or for an entire team at an organization, GridGain Training is the fastest and most cost-effective way to become an in-memory computing platform expert.”

GridGain Training – Foundation Courses

Register for these complimentary 2-hour virtual programs at https://www.gridgain.com/training.

  • Apache Ignite Essentials: Key Design Principles for Building Data-Intensive Applications – A two-hour training program that introduces three essential Ignite capabilities – data partitioning, affinity co-location, and co-located processing – and shows how these capabilities increase application speed and scale.

    • 03/17/21 – 10 a.m. PDT
    • 04/14/21 – 8 a.m. GMT
    • 05/24/21 – 8 a.m. PDT
  • How to Monitor and Manage Apache Ignite with GridGain Control Center – A two-hour, hands-on training session on how to monitor and manage Apache Ignite clusters in production, including understanding key metrics, setting up alerts, and troubleshooting performance.

    • 03/24/21 – 10 a.m. PDT
    • 04/21/21 – 8 a.m. GMT
    • 05/24/21 – 10 a.m. PDT
  • Apache Ignite for Spring Boot and Spring Data Development – A two-hour training program for Java developers and architects who want to explore best practices and nuances of using Spring Boot and Spring Data with Apache Ignite. Attendees will build a RESTful web service that uses Apache Ignite as an in-memory database.

    • 04/07/21 – 10 a.m. PDT

GridGain Training – Certification Courses
These virtual, intensive programs offer more hands-on training in smaller groups. Attendees who successfully complete these classes will earn GridGain certificates. Register at https://www.gridgain.com/training.

  • Apache Ignite Platform Training – A full-day hands-on course designed to provide an overview of the Apache Ignite platform, covering basic product functionality, common use-cases and APIs. Attendees will participate in lab exercises to reinforce the learning.

    • 4/29/21 – 8 a.m. to 4 p.m. PDT
    • Cost: $1,000 USD per attendee
  • GridGain Developer Training – This 3-day course, geared to help attendees architect and build scalable applications using the GridGain platform, will cover basic and advanced platform functionality, available APIs, tools and utilities through a series of lectures and hands-on lab exercises.

    • 5/18/21-5/20/21 – 8 a.m. to 4 p.m. PDT
    • Cost: $3,000 USD per attendee
  • GridGain Administrator Training – This 3-day course will provide a deeper understanding of the GridGain features, capabilities and utilities for monitoring, maintaining and administering the GridGain platform. Through a series of interactive sessions and hands-on lab exercises, attendees will learn to perform upgrades, tune and secure the GridGain cluster, perform cluster and data backup and restore tasks, and debug and troubleshoot any issues that may come up.
    • 6/8/21-6/10/21 – 8 a.m. to 4 p.m. PDT
    • Cost: $3,000 USD per attendee

GridGain Corporate Training

For business customers and partners, certification courses are offered at group rates and at convenient times. This is a cost-effective way to train a team of developers, architects, or administrators from the same organization to accelerate the pace of deployment, ensure optimal use of the platform and enable effective troubleshooting. Available in a virtual or on-site format, each private training program is led by a seasoned GridGain product specialist and enables attendees to discuss issues and challenges that are specific to their organization.

For more information about Corporate Training options, contact GridGain at https://www.gridgain.com/contact.

Additional Resources

To learn more about the GridGain in-memory computing platform:  

About GridGain Systems

GridGain Systems is revolutionizing real-time data access and processing by offering the leading in-memory computing platform, powered by the Apache® Ignite® distributed database. Common use cases for the GridGain platform include application acceleration and digital integration hubs for real-time data access across data sources and applications. GridGain solutions are used by global enterprises in financial services, software, e-commerce, retail, online business services, healthcare, telecom, transportation and other major sectors, with a client list that includes ING, Citibank, American Express, Finastra, UPS, Hewlett Packard Enterprise, Microsoft, American Airlines, Agilent and UnitedHealthcare.

GridGain delivers unprecedented speed, massive scalability, and real-time data access for both legacy and greenfield applications. Deployed on a distributed cluster of commodity servers, GridGain software can reside between the application and data layers (RDBMS, NoSQL and Apache® Hadoop®), requiring no rip-and-replace of the existing databases, or it can be deployed as a distributed database for high performance computing with in-memory speed. For more information, visit gridgain.com.

CONTACT:

Brigit Valencia
For GridGain Systems
[email protected]
(360) 597-4516

The Apache Software Foundation has no affiliation with and does not endorse, or review the materials provided in these training courses.

GridGain is a trademark or registered trademark of GridGain Systems, Inc. Apache, Apache Ignite, and Ignite are trademarks of The Apache Software Foundation. All other product and company names herein may be trademarks of their registered owners.



Independence Gold Recovers Up to 97.9% Gold From 3Ts Property, British Columbia

VANCOUVER, British Columbia, March 04, 2021 (GLOBE NEWSWIRE) — Independence Gold Corp. (TSX.V: IGO) (“Independence” or “the Company”) is pleased to announce the results from metallurgical test work completed on mineralized quartz vein material from its 100% owned 3Ts Project, located approximately 185 kilometres (“km”) southwest of Prince George, British Columbia and situated 20 km southwest of Artemis Gold Inc.’s Blackwater Project.

This study was initiated to confirm the results from a previous metallurgical study conducted for Independence by SGS Canada Inc. (see news release dated July 9th, 2013). This study used composite sample from drill core material from the Ted-Mint vein system and subjected it to a three-stage recovery (gravity, floatation, and cyanide leaching). The 2013 study yielded 97.3% gold recovery and 94.9% silver recovery.

Sample Selection and Preparation

Composite samples comprised of sample rejects of mineralized vein material were collected from drill core recovered during the 2020 program. The first composite comprised material from the Tommy Vein (drill holes 3T-20-01 and 3T-20-02), and the second composite from the Ted-Mint offset vein (drill hole 3T-20-10). These veins yielded gold assay values up to 68.7 grams per tonne (“g/t”) and silver assay values up to 2,550 g/t from meter-scale samples (see news release dated November 4th, 2019).

Head Results

The following table summarizes the assays results for both composite samples:

Sample

Screened Metallics
Au g/t Ag g/t
Composite 1 (Tommy Vein) 4.9 34.3
Composite 2 (Ted-Mint Offset Vein) 4.2 139.0

The metallurgical study from 2013 returned head results 2.28 g/t gold and 66.6 g/t silver from the Ted-Mint vein, therefore the 2021 results appear to show an improvement in grade.

Gravity Separation
A single gravity separation test was completed on each composite to evaluate the potential for gravity recoverable gold and silver using a Knelson concentrator. The initial concentrate was then further upgraded to a Mozley shaking table. The Mozley concentrate was submitted for assaying and the tailings used for floatation testing. Gravity methods were poor in Composite 1, managing to recover 1.46% gold and 0.57% silver. Composite 2 showed improved recovery for gold with 27.6%, but silver recovery remained low at 3.62%.

Floatation Testwork

A single test was conducted on each of the gravity tailings to assess further recoverability of gold and silver, with the concentrate being submitted for assaying and mineralogy. From these tailings, Composite 1 recovered 76.0% gold and 74.8% silver remaining in the stream, while Composite 2 recovered 64.1% gold and 84.8% silver.

Cyanide Leaching
The floatation tailings were submitted for bottle roll cyanide leaching tests, lasting for 48-hours with a pH of 10.5 to 11. Both composites performed well and recovered additional gold in the pregnant leach solution. Composite 1 recovered 16.4% gold and 17.1% silver from the floatation tailings, while Composite 2 recovered 6.18% gold and 7.07% silver.

Overall Results

The following table summarizes the results of the metallurgical test work:

  Composite 1 (Tommy Vein) Composite 2 (Ted-Mint Offset Vein)
Total Gold
Recovery
Total Silver
Recovery
Total Gold
Recovery
Total Silver
Recovery
Gravity Concentrate 1.46%   0.57%   27.6%   3.62%  
Floatation Concentrate 76.0%   74.8%   64.1%   84.8%  
Leach Concentrate 16.4%   17.1%   6.18%   7.07%  
TOTAL RECOVERY 93.9
%
  92.4
%
  97.9
%
  95.5
%
 

It is believed that recoverability could be further improved by modifying the processes and with additional mineralogical studies to understand deportment of the gold and silver within the Tommy Vein compared to the Ted-Mint Offset Vein.

Methodology

Samples rejects were blended, crushed to minus 10-micron mesh, and split into 2 kilogram (“kg”) and 10 kg test charges. For each composite, a 2 kg test charge was selected at random and submitted for head chemical and screened metallics. The 2 kg test charges were split into two, with the first half being used for gold and silver analysis by the screened metallics protocol. The sample was stage pulverized to pass a 150 mesh screen until less than 30 grams remained in the oversize fraction. The oversize fraction, as well as two representative cuts of the undersize, were submitted for gold and silver analysis by fire assay to extinction.


About Independence

Independence Gold Corp. (TSX.V:IGO) is a mineral exploration company listed on the TSX Venture Exchange. The Company’s holdings range from early-stage grassroots exploration to advanced-stage resource expansion in British Columbia and Yukon. For additional information, visit the Company’s website www.ingold.ca.

Andy Randell, P.Geo., the Company’s Qualified Person as defined by National Instrument 43-101, has reviewed the technical information in this news release.

ON BEHALF OF THE BOARD OF INDEPENDENCE GOLD CORP.

“Randy Turner”

Randy Turner, President & CEO

Neither the TSX Venture Exchange nor its Regulation Services Provider (as that term is defined in policies of the TSX Venture Exchange) accepts responsibility for the adequacy or accuracy of this release.

All statements in this press release, other than statements of historical fact, are “forward-looking information” with respect to Independence within the meaning of applicable securities laws, including statements with respect to the Company’s planned drilling and exploration activities. The Company provides forward-looking statements for the purpose of conveying information about current expectations and plans relating to the future and readers are cautioned that such statements may not be appropriate for other purposes. By its nature, this information is subject to inherent risks and uncertainties that may be general or specific and which give rise to the possibility that expectations, forecasts, predictions, projections or conclusions will not prove to be accurate, that assumptions may not be correct and that objectives, strategic goals and priorities will not be achieved. These risks and uncertainties include but are not limited to those identified and reported in Independence’s public filings under Independence Gold Corp.’s SEDAR profile at
www.sedar.com
.  Although Independence has attempted to identify important factors that could cause actual actions, events or results to differ materially from those described in forward-looking information, there may be other factors that cause actions, events or results not to be as anticipated, estimated or intended. There can be no assurance that such information will prove to be accurate as actual results and future events could differ materially from those anticipated in such statements. Independence disclaims any intention or obligation to update or revise any forward-looking information, whether as a result of new information, future events or otherwise unless required by law. 

Contact:
Telephone: 604-687-3959
Facsimile: 604-687-1448
E-Mail: [email protected] 



TALOS WELCOMES ALFONSE MANDESE AS HEAD OF SALES AND BUSINESS DEVELOPMENT

Institutional crypto trading platform expands team following successful 2020

New York, NY, March 04, 2021 (GLOBE NEWSWIRE) — Talos, an end-to-end technology infrastructure provider that supports the institutional trading of digital assets, today announced the hire of Alfonse Mandese as Head of Sales and Business Development.

Mr. Mandese will be responsible for executing Talos’ go-to-market strategy, building partnerships and driving future revenue growth. Mr. Mandese’s hire comes at a time of tremendous growth for the Talos platform, which has been live since early 2019 and was publicly announced last fall. Talos’ extensive suite of solutions supports clients through the full crypto trading lifecycle, from price discovery to execution through clearing and settlement and across spot, futures and FX markets.

Prior to joining Talos, Mr. Mandese led sales and business development in the Americas for Ledger Enterprise Solutions. There, he focused on the rollout of the company’s enterprise custody technology product, Ledger Vault. Before that, Mr. Mandese spent seven years in the traditional capital markets space. He formerly held positions across Institutional Sales and Trading at Citigroup in both New York and Boston. After Citi, he became a Regional Head of Account Management and Business Development at BCA Research. At both companies, he covered some of the world’s leading asset managers and hedge funds. He holds a degree in Economics from Franklin & Marshall College.

Commenting on Mr. Mandese’s hire, Talos Co-Founder and CEO Anton Katz said: “The acceleration of institutional participation in digital assets over the past year has completely transformed our firm. As large institutions and service providers continue to enter this space and use our platform, we are really excited to have Alfonse join the team and lead our Business Development and Sales efforts going forward. His portfolio of experience has the ideal combination of traditional capital markets and institutional crypto, which will be crucial to our ongoing effort to scale our business. We could not be more excited to have him as part of our team, and look forward to setting the bar even higher in 2021.”

Mr. Mandese said: “Having worked in business development and sales within both the traditional finance and digital assets space, I’ve had the opportunity to learn the importance of a defined, yet flexible, growth strategy that will position me to thrive in this role. Talos’ recent success is nothing short of inspiring and I am looking forward to contributing to the company’s continued expansion. Anton Katz, Ethan Feldman and the Talos team have built an offering unlike anything this industry has seen before. Talos is truly pioneering the institutional crypto space, and I’m eager to get started.”

  

About Talos

Talos provides an institutional-grade technology infrastructure that supports the full lifecycle of digital assets trading, from price discovery to execution through to settlement. Engineered by a team with unmatched experience building institutional trading systems, the Talos platform connects the diverse group of participants involved in today’s crypto-asset market structure – institutional investors, prime brokers, exchanges, OTC desks, lenders, and custodians – through a single point of entry. This streamlines the entire trading process, eliminates unnecessary intermediary risk, and provides institutions a clear path to best execution. For additional information, visit www.talos.com.



Richard Franco
Forefront Communications for Talos
917-309-8951
[email protected]

Fortress Biotech to Participate in Four March 2021 Virtual Investor Conferences

NEW YORK, March 04, 2021 (GLOBE NEWSWIRE) — Fortress Biotech, Inc. (NASDAQ: FBIO) (“Fortress”), an innovative revenue-generating company focused on acquiring, developing and commercializing or monetizing promising biopharmaceutical products and product candidates cost-effectively, today announced that Lindsay A. Rosenwald, M.D., Chairman, President and Chief Executive Officer, will participate in four virtual investor conferences in March 2021.

Details of the events are as follows:

  • H.C. Wainwright Global Life Sciences Virtual Conference: The company’s presentation will be available for on-demand viewing on Fortress’ website beginning on Tuesday, March 9, 2021, at 7:00 a.m. ET and will remain available on the Events page under the News & Media section of Fortress’ website: www.fortressbiotech.com for approximately 30 days following the presentation.
  • Barclays Global Healthcare Virtual Conference: The company will present on Thursday, March 11, 2021, at 3:00 p.m. ET and will participate in one-on-one meetings during the conference.
  • Virtual 33rd Annual ROTH Conference: The company will participate in a fireside chat on Tuesday, March 16, 2021, at 11:00 AM ET and will attend one-on-one meetings during the conference. A webcast of the fireside chat will be available on the Events page under the News & Media section of Fortress’ website: www.fortressbiotech.com for approximately 30 days following the chat.
  • Oppenheimer 31st Annual Virtual Healthcare Conference: The company will present on Thursday, March 18, 2021, at 10:40 a.m. ET and will participate in one-on-one meetings during the conference.

About Fortress Biotech

Fortress Biotech, Inc. (“Fortress”) is an innovative biopharmaceutical company that was ranked in Deloitte’s 2019 and 2020 Technology Fast 500™, annual rankings of the fastest-growing North American companies in the technology, media, telecommunications, life sciences and energy tech sectors, based on percentages of fiscal year revenue growth over three-year periods. Fortress is focused on acquiring, developing and commercializing high-potential marketed and development-stage drugs and drug candidates. The company has five marketed prescription pharmaceutical products and over 25 programs in development at Fortress, at its majority-owned and majority-controlled partners and at partners it founded and in which it holds significant minority ownership positions. Such product candidates span six large-market areas, including oncology, rare diseases and gene therapy, which allow it to create value for shareholders. Fortress advances its diversified pipeline through a streamlined operating structure that fosters efficient drug development. The Fortress model is driven by a world-class business development team that is focused on leveraging its significant biopharmaceutical industry expertise to further expand the company’s portfolio of product opportunities. Fortress has established partnerships with some of the world’s leading academic research institutions and biopharmaceutical companies to maximize each opportunity to its full potential, including Alexion Pharmaceuticals, Inc., AstraZeneca, City of Hope, Fred Hutchinson Cancer Research Center, St. Jude Children’s Research Hospital and Nationwide Children’s Hospital. For more information, visit www.fortressbiotech.com.

Forward-Looking Statements

This press release may contain “forward-looking statements” within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934, as amended. As used below and throughout this press release, the words “we”, “us” and “our” may refer to Fortress individually or together with one or more partner companies, as dictated by context. Such statements include, but are not limited to, any statements relating to our growth strategy and product development programs and any other statements that are not historical facts. Forward-looking statements are based on management’s current expectations and are subject to risks and uncertainties that could negatively affect our business, operating results, financial condition and stock price. Factors that could cause actual results to differ materially from those currently anticipated include: risks relating to our growth strategy; our ability to obtain, perform under and maintain financing and strategic agreements and relationships; risks relating to the results of research and development activities; uncertainties relating to preclinical and clinical testing; risks relating to the timing of starting and completing clinical trials; our dependence on third-party suppliers; risks relating to the COVID-19 outbreak and its potential impact on our employees’ and consultants’ ability to complete work in a timely manner and on our ability to obtain additional financing on favorable terms or at all; our ability to attract, integrate and retain key personnel; the early stage of products under development; our need for substantial additional funds; government regulation; patent and intellectual property matters; competition; as well as other risks described in our SEC filings. We expressly disclaim any obligation or undertaking to release publicly any updates or revisions to any forward-looking statements contained herein to reflect any change in our expectations or any changes in events, conditions or circumstances on which any such statement is based, except as may be required by law, and we claim the protection of the safe harbor for forward-looking statements contained in the Private Securities Litigation Reform Act of 1995. The information contained herein is intended to be reviewed in its totality, and any stipulations, conditions or provisos that apply to a given piece of information in one part of this press release should be read as applying mutatis mutandis to every other instance of such information appearing herein.

Company Contacts:

Jaclyn Jaffe and William Begien
Fortress Biotech, Inc.
(781) 652-4500
[email protected]

Investor Relations Contact:

Daniel Ferry
LifeSci Advisors, LLC
(617) 430-7576
[email protected]

Media Relations Contact:

Tony Plohoros
6 Degrees
(908) 591-2839
[email protected]  



Herborium® Group Inc. Skin Health Products to Enter $250 Million Pacific Asian Market

Unique Acne Treatment AcnEase® to Target Half a Billion Consumers

Houston, March 04, 2021 (GLOBE NEWSWIRE) —  March 4, 2021 Houston, Texas. Herborium® Group, Inc. (OTC Pink: HBRM),  www.Herborium.com, www.acnease.com a Botanical Therapeutics® Company and the provider of proprietary, all botanical medicinal products (Botanical Therapeutics®) and interactive advanced content targeting dermatological concerns including  acne, oily skin, acne scars,  Rosacea and skin aging and health , as well as other health and wellness concerns, is happy to announce its unique herbal acne treatment -AcnEase® to enter the fastest growing Asia Pacific market.

As the global dietary supplements market is poised to grow by $26.7 billion during the period spanning 2020-2024, the major shift lies in where this growth will come from. In 2017, 31% of the world’s consumer disposable income originates from Asia. By 2030, Asia is expected to add an additional USD12 trillion in disposable income, which is almost 55% of the global increment. The Asian skincare market is expected to grow by 6% by 2022. South East Asia also has a high percent of the young people between 15-24 year of age that constitute the most promising target market for AcnEase. This market, across the region but excluding India and Russia but including Australia, is about 0.5 billion individuals. Targeting just 0.5% of this population with a minimal sales of 5 bottles a year and the 75% price reduction in comparison to US market, provides for the estimated market potential of $250 Million.

To harness this opportunity, Herborium ®signed a distribution agreement with Phinix Global Pte. Ltd. (“Phinix”).  Phinix Global Pte. Ltd. is a part of GPS Alliance Holdings Limited (AU:GPS) which is listed on the Sydney Stock Exchange. GPS has extensive reach throughout South East Asia .  We expect the sales of AcnEase to commence in South East Asia in early 3rd quarter of 2021. In addition to marketing and distributing Herborium’s products Herborium and GPS are presently discussing additional partnership to foster Herborium stronger presence in South East Asia and possibly – the company presence on South East Asia capital markets.

About Herborium Group, Inc.

Herborium Group, Inc. is a botanical therapeutics® company that develops, licenses and markets proprietary, botanical based medicinal products to consumers and healthcare professionals. The Company’s business model focuses on emerging market opportunities spearheaded by the growth of a new market sector located between high-cost, high-risk, ethical pharmaceuticals and commoditized classic nutraceuticals (supplements).  The Company uses clinical validation,  a proactive regulatory strategy and a innovative , interactive content to establish and maintain a differential advantage.  Herborium has secured a pipeline of botanical ingredients based products Herborium Group sells its products in the United States, the United Kingdom, and continental Europe through a network of distributors, specialty retailers, and e-commerce. For more information, please visit www.herborium.com, www.acnease.com , www.acnease.fr,   and www.acnease.eu    

Safe Harbor Statement:  This release contains forward-looking statements with respect to the results of operations and business of Herborium Group, Inc., which involves risks and uncertainties.  The Company’s actual future results could materially differ from those discussed.   The Company intends that such statements about the Company’s future expectations, including future revenues and earnings, and all other forward looking statements be subject to the “Safe Harbors” provision of the Private Securities Litigation Reform Act of 1995.

Attachment



Contact Information:

Herborium Group, Inc.

Email: [email protected]  or [email protected]