Rhode Island Stop & Shop Pharmacies Now Accepting Walk-Ins for COVID-19 Vaccines

QUINCY, Mass., May 04, 2021 (GLOBE NEWSWIRE) — Stop & Shop, in conjunction with the U.S. Department of Health & Human Services (HHS) and the Rhode Island Department of Health, announced that all 14 of its Rhode Island pharmacy locations are now accepting walk-ins for the COVID-19 vaccine. Customers can still schedule appointments on Stop & Shop’s website, but appointments are no longer required to receive an immunization.

Stop & Shop operates 14 pharmacies across Rhode Island, each offering either the Moderna or Johnson & Johnson (Janssen) vaccine. Customers can walk in and receive a COVID-19 vaccine at any of the following locations, though walk-ins will be determined by supply levels.

  • Cranston (Atwood Ave)        
  • Cranston (Garfield Ave)        
  • Cumberland (Mendon Road)
  • East Providence (Pawtucket Avenue)
  • Greenville (Putnam Pike)
  • Lincoln (George Washington Highway)        
  • Middletown (West Main Road)
  • North Providence (Mineral Spring Avenue)
  • North Smithfield (Smithfield Road)
  • Narragansett (Point Judith Road)
  • Pawtucket (Cottage Street)
  • Providence (Manton Avenue)
  • Warwick (Quaker Lane)        
  • Warwick (Warwick Ave)

“Stop & Shop has been proud to support Rhode Islanders throughout the pandemic, most recently by administering the COVID-19 vaccine,” said Katie Thornell, Director of Pharmacy Operations at Stop & Shop. “We are prepared to continue helping members of the community protect themselves against COVID-19 by allowing all Rhode Islanders the convenience of walking into any of our Rhode Island pharmacies to receive their immunization without needing an appointment.”

In December, Stop & Shop announced a partnership with the U.S. Department of Health & Human Services (HHS) to be among the first COVID-19 vaccine providers, making the shot available to its customers across the Northeast. The coronavirus vaccine is being administered at no out-of-pocket cost.

During immunization, customers will be required to wear PPE and pharmacists will be equipped with masks, gloves, and face shields. The pharmacy team utilizes the same thorough disinfection protocols for all patients, disinfecting and sanitizing between each patient to ensure the health & safety for all patients.

Flu, pneumonia, shingles and other immunizations are currently available to customers at all Stop & Shop Pharmacy locations. To find your nearest Stop & Shop pharmacy, visit www.stopandshop.com/pharmacy. For more information on Stop & Shop’s rollout of the COVID-19 vaccine, visit www.stopandshop.com/covid-vaccine.

About Stop & Shop:

A neighborhood grocer for more than 100 years, Stop & Shop is focused on delivering a wide assortment of fresh, healthy options at a great value through strong weekly sales and everyday low prices. Its new GO Rewards loyalty program delivers personalized offers and allows customers to earn points that can be redeemed for gas or groceries every time they shop. Stop & Shop customers can choose however they want to shop – whether it’s in-store or online, which offers both delivery and same day pickup. The company is committed to making an impact in its communities by fighting against hunger, supporting our troops and through overall incredible acts of care. The Stop & Shop Supermarket Company LLC is an Ahold Delhaize USA Company and employs 58,000 associates and operates more than 400 stores throughout Massachusetts, Connecticut, Rhode Island, New York and New Jersey. To learn more about Stop & Shop, visit www.stopandshop.com.

Media Contact:
Maria Fruci, [email protected]



PCT LTD Conveys Current Status of OTC QB Uplisting Efforts

PCT LTD Conveys Current Status of OTC QB Uplisting Efforts

LITTLE RIVER, S.C.–(BUSINESS WIRE)–
PCT LTD (“PCTL” OTC Pink) reports that its application to have its common stock quoted on OTC Markets, “QB” level, has been declined due to OTC’s requirements for PCTL to complete all prior settlement agreement terms and clear all other potentially dilutive (“toxic”) debt.

The Company’s CEO, Gary Grieco, commented, “We learned OTC Markets declined to accept our application for quotation on its QB tier for ‘various reasons,’ primarily having to do with prior convertible debt and the incremental settlement of such.” Grieco further commented, “We managed to bring the Company out of the throes of some difficult debt and we will continue to replace that type of debt with our growing revenues from licensing, fluids sales, equipment sales and other financial resources, such as RB Capital.”

PCT LTD intends to continue as a current and reporting OCT Pink company as it prepares for a September 2021 re-application for the OTC:QB quotation.

About PCT LTD:

PCT LTD (“PCTL”) focuses its business on acquiring, developing and providing sustainable, environmentally safe disinfecting, cleaning and tracking technologies. The company acquires and holds rights to innovative products and technologies, which are commercialized through its wholly-owned operating subsidiary, Paradigm Convergence Technologies Corporation (PCT Corp). The Company established entry into its target markets with commercially viable products in the United States and now continues to gain market share in the U.S. and U.K.

ADDITIONAL NEWS AND CORPORATE UPDATES:

PCTL would like to warn its stockholders and potential investors that material corporate information regarding sales, areas of business and other corporate updates will only be made through press releases or filings with the SEC. PCTL does not utilize social media, chatrooms or other online sources to disclose material information. The public should only rely on official press releases and corporate filings for accurate and up to date information regarding PCTL.

Forward-Looking Statements:

This press release contains “forward-looking statements” as defined in Section 27A of the Securities Act of 1933, as amended, and Section 21B of the Securities Exchange Act of 1934, as amended. Any statements that express or involve discussions with respect to predictions, expectations, beliefs, plans, projections, objectives, goals, assumptions or future events or performance are not statements of historical fact and may be “forward-looking statements.”

Such statements are based on expectations, estimates and projections at the time the statements are made that involve a number of risks and uncertainties, which could cause actual results or events to differ materially from those presently anticipated. Such statements involve risks and uncertainties, including but not limited to: PCTL’s ability to raise sufficient funds to satisfy its working capital requirements; the ability of PCTL to execute its business plan; the anticipated results of business contracts with regard to revenue; and any other effects resulting from the information disclosed above; risks and effects of legal and administrative proceedings and government regulation; future financial and operational results; competition; general economic conditions; and the ability to manage and continue growth. Should one or more of these risks or uncertainties materialize, or should underlying assumptions prove incorrect, actual outcomes may vary materially from those indicated. Important factors that could cause actual results to differ materially from the forward-looking statements PCTL makes in this press release include market conditions and those set forth in reports or documents it files from time to time with the SEC. PCTL undertakes no obligation to revise or update such statements to reflect current events or circumstances after the date hereof or to reflect the occurrence of unanticipated events.

Investor Relations Contact

Andrew Barwicki

(516) 662-9461

[email protected]

or

[email protected]

www.para-con.com

www.pctcorphealth.com

Twitter: https://mobile.twitter.com/PCTL2021

KEYWORDS: United States North America South Carolina

INDUSTRY KEYWORDS: Medical Supplies Chemicals/Plastics Medical Devices Health Infectious Diseases Manufacturing

MEDIA:

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FIBRA Prologis Refinances US$370 million through a Green Private Placement in the US and a Green Bond in the Local Market

PR Newswire

MEXICO CITY, May 4, 2021 /PRNewswire/ — FIBRA Prologis (BMV: FIBRAPL 14), a leading owner and operator of Class-A industrial real estate in Mexico, announced today that it raised US$370 million dollars through a US$300 million green US Private Placement of senior unsecured notes (“USPP”) and a US$70 million dollars equivalent green bond offering of Long Term Trust Certificates “Certificados Bursátiles Fiduciarios de Largo Plazo” (BMV: FIBRAPL 21DV) (the “Notes”).

  • The USPP have a weighted average interest expense, including the estimated corresponding withholding tax, of approximately 3.65% per annum and are senior, unsecured obligations of FIBRAPL.
  • The Notes bear interest of approximately 3.73% per annum, and are senior, unsecured obligations of FIBRAPL.

Net proceeds from both transactions will be used to fund the repayment of term loans that are due in 2023 and 2024, and paydown outstanding borrowings on FIBRAPL’s line of credit, that were used to finance in whole or in part our “Eligible Green Project Portfolio” as defined in the CEBURES offering’s prospectus supplement.

“We are very pleased to continue increasing FIBRAPL’s green financings through various efficient and flexible types of debt, resulting in an even stronger balance sheet,” said Jorge Girault, Senior Vice-President, Fund Asset Management Prologis Property Mexico. “I am grateful for the trust put in us by our Mexican and international investors in both transactions. This refinancing opens new possibilities for us in the capital markets, with new, international investors coming into Mexico and improving the execution of all our financing options.”

ABOUT FIBRA PROLOGIS

FIBRA Prologis is a leading owner and operator of Class-A industrial real estate in Mexico. As of March 31, 2021, FIBRA Prologis was comprised of 205 logistics and manufacturing facilities in six industrial markets in Mexico totaling 40.1 million square feet (3.7 million square meters) of gross leasable area.

FORWARD-LOOKING STATEMENTS

The statements in this release that are not historical facts are forward-looking statements. These forward-looking statements are based on current expectations, estimates and projections about the industry and markets in which FIBRA Prologis operates, management’s beliefs and assumptions made by management.  Such statements involve uncertainties that could significantly impact FIBRA Prologis financial results. Words such as “expects,” “anticipates,” “intends,” “plans,” “believes,” “seeks,” “estimates,” variations of such words and similar expressions are intended to identify such forward-looking statements, which generally are not historical in nature.  All statements that address operating performance, events or developments that we expect or anticipate will occur in the future — including statements relating to rent and occupancy growth, acquisition activity, development activity, disposition activity, general conditions in the geographic areas where we operate, our debt and financial position, are forward-looking statements. These statements are not guarantees of future performance and involve certain risks, uncertainties and assumptions that are difficult to predict. Although we believe the expectations reflected in any forward-looking statements are based on reasonable assumptions, we can give no assurance that our expectations will be attained and therefore, actual outcomes and results may differ materially from what is expressed or forecasted in such forward-looking statements. Some of the factors that may affect outcomes and results include, but are not limited to: (i) national, international, regional and local economic climates, (ii) changes in financial markets, interest rates and foreign currency exchange rates, (iii) increased or unanticipated competition for our properties, (iv) risks associated with acquisitions, dispositions and development of properties, (v) maintenance of real estate investment trust (“FIBRA”) status and tax structuring, (vi) availability of financing and capital, the levels of debt that we maintain and our credit ratings, (vii) risks related to our investments (viii) environmental uncertainties, including risks of natural disasters, (ix) risks related to the coronavirus pandemic, and (x) those additional factors discussed in reports filed with the “Comisión Nacional Bancaria y de Valores” and  the Mexican Stock Exchange by FIBRA Prologis under the heading “Risk Factors.” FIBRA Prologis undertakes no duty to update any forward-looking statements appearing in this release.

Non-Solicitation – Any securities discussed herein or in the accompanying presentations, if any, have not been registered under the Securities Act of 1933 or the securities laws of any state and may not be offered or sold in the United States absent registration or an applicable exemption from the registration requirements under the Securities Act and any applicable state securities laws. Any such announcement does not constitute an offer to sell or the solicitation of an offer to buy the securities discussed herein or in the presentations, if and as applicable.

 

 

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SOURCE FIBRA Prologis

22nd Century Group and KeyGene Extend and Expand Plant Research Partnership

Updated Agreement Extends Exclusive Program to Create Valuable, New Hemp/Cannabis Varieties and Expands Collaboration to Include 22nd Century’s Two Other Plant Franchises

Partnerships Will Enable 22nd Century to Accelerate the New Development of Valuable, Commercial Hemp/Cannabis Lines and Intellectual Property to Market in Two Years

BUFFALO, N.Y., May 04, 2021 (GLOBE NEWSWIRE) — 22nd Century Group, Inc. (NYSE American: XXII), a leading plant-based biotechnology company focused on tobacco harm reduction, very low nicotine content tobacco, and hemp/cannabis research, announced today that it has reached an agreement to extend and expand its successful plant research partnership agreement with KeyGene, a global leader in plant research involving high-value genetic traits and increased crop yields. The new partnership agreement extends the length of the exclusive worldwide collaboration 22nd Century has with KeyGene to develop new, disruptive hemp/cannabis plants and intellectual property for the life science, medicinal, and pharmaceutical end-use markets. It also expands the partnership to include research and development activity for non-combustible, alternative tobacco plant applications, such as protein production, and 22nd Century’s third plant franchise, plus it establishes a new governance structure and working model to accelerate development timelines across all three crop/trait programs.

“We have a highly successful relationship with KeyGene, and we are excited to announce this expansion of our partnership that we have been referring to recently,” said James A. Mish, chief executive officer of 22nd Century Group. “Our KeyGene partnership has proven to be crucial for 22nd Century’s growth and success in the hemp/cannabis space. Since launching our collaboration in 2019, we have achieved much together, including a breakthrough in molecular breeding that will significantly reduce the time needed to develop new hemp/cannabis plant lines with commercially valuable traits. We are pleased to extend our exclusive, global hemp/cannabis research agreement with KeyGene and expand our partnership with KeyGene’s world-class team of plant scientists, geneticists, molecular biologists, and bioinformaticians to achieve the same levels of success with biotechnology applications for plant-based protein production as well as our yet-to-be-announced third plant franchise.“

“Our partnership with 22nd Century Group has been mutually beneficial, as we have worked together to make game-changing discoveries in hemp/cannabis genetic research,” said Walter Nelson, chief executive officer of KeyGene USA. “This expanded partnership fits well into KeyGene’s push into integrating metabolomics and proteomics with our capabilities in genomics using innovative informatics tools. I am excited to build on this successful relationship and look forward to what we will be able to accomplish in other crops using our technology innovation platforms.”

Through this successful, expanded partnership, 22nd Century has access to KeyGene’s unique suite of crop innovation platforms, including genomics, molecular breeding, trait discovery, and metabolomics technologies. KeyGene’s team of scientists also possess unmatched expertise and a strong track record of success in plant biotechnology, providing 22nd Century the ability to co-develop groundbreaking genetic solutions for commercial traits in plant technology that differentiate it from other plant-based biotechnology companies.

“We have worked with KeyGene to develop platforms and tools that have allowed us to identify plant lines with unique profiles of various major cannabinoids in hemp/cannabis plants. We also found that these strains have minor cannabinoids that may have potential medicinal applications. This expanded partnership will give us the exclusive rights to develop and commercialize these unique cannabinoids traits,” said Juan Sanchez Tamburrino, vice president of research and development at 22nd Century Group.

The renewed partnership will help to accelerate the development of new plant lines across 22nd Century’s three franchises by enhancing the working process between the two organizations. 22nd Century and KeyGene will form an executive steering committee to establish and refine targeted traits, technologies, intellectual property, and other deliverables and ensure collaboration achieves its objectives and timelines. With the extended and expanded partnership with KeyGene, 22nd Century has secured and enhanced four of the five key partnerships needed in the upstream segments of the cannabinoid value chain. Combining the Company’s core strength in plant science and its network of operational partnerships will enable 22nd Century to drive differentiation and value by delivering new valuable plant lines and IP in two years. The Company will tailor its solutions for the hemp/cannabis industry to the unique needs of its customers and consumers across a wide range of end-use markets, including the life science, consumer product, and pharmaceutical industries.

22nd Century’s hemp/cannabis strategy targets the upstream segments of the cannabinoid value chain and related intellectual property in the areas of plant biotechnology research, gene modification and engineering, modern plant breeding and development, and extraction. The Company is focused on developing intellectual property and proprietary hemp/cannabis plants with high-value genetic and agronomic traits, including lines with stable, ultra-high specific cannabinoid levels, lines with rare cannabinoids, and lines with ultra-high and ultra-low terpene levels. This new agreement with KeyGene aligns with the Company’s focus and its updated strategy to be more aggressive with the development of commercially valuable hemp/cannabis lines.

22nd Century also believes the new agreement with KeyGene will place the two organizations in a better position to build on their partnership’s success to date. Over the past year, KeyGene and 22nd Century have made tremendous progress in hemp/cannabis research. In March 2020, the Company announced that it built a proprietary bioinformatics platform, allowing 22nd Century to monetize a portion of the vast knowledge foundation and intellectual property it has developed. In February of this year, the partners announced the launch of an advanced cannabis biotechnology platform that will enable 22nd Century and its strategic partners to quickly identify and incorporate commercially valuable traits into new, stable hemp/cannabis lines to be commercialized in two-year cycles. The platform includes a suite of proprietary molecular tools and an extensive library of reference genomes, molecular markers, and gene-trait correlations that the Company will begin to monetize by later this year. 22nd Century has already characterized millions of high-value single nucleotide polymorphisms (SNPs). By targeting SNPs newly identified through this platform, the Company has sequenced large numbers of cannabis varieties and assembled them into reference genomes. This has enabled 22nd Century to find the genes responsible quickly and easily for specific traits in a plant, proving the power of this tool for the Company and the hemp/cannabis industry.

22nd Century’s third franchise, with a total addressable market of $500 billion, operates in an industry less regulated than tobacco and hemp/cannabis. It is large, growing, and a natural extension of the Company’s core strength and expertise with a faster route to commercialization than the Company’s first two franchises. The third franchise also has a similar genome to the hemp/cannabis plant. 22nd Century is leveraging its know-how in plant science, securing valuable intellectual property, and pursuing strategic partnerships to support the development of this franchise. Combined, 22nd Century’s three franchises have a total addressable market of well over $1.3 trillion. There is a natural intersection of adjacencies across 22nd Century’s three plant-based franchises. The Company will turn attention to the development of its third, plant-based franchise after securing MRTP authorization for VLN®.

About 22nd Century Group, Inc.

22nd Century Group, Inc. (NYSE American: XXII) is a leading plant biotechnology company focused on technologies that alter the level of nicotine in tobacco plants and the level of cannabinoids in hemp/cannabis plants through genetic engineering, gene-editing, and modern plant breeding. 22nd Century’s primary mission in tobacco is to reduce the harm caused by smoking through the Company’s proprietary reduced nicotine content tobacco cigarettes – containing 95% less nicotine than conventional cigarettes. The Company’s primary mission in hemp/cannabis is to develop and commercialize proprietary hemp/cannabis plants with valuable cannabinoid profiles and desirable agronomic traits.

Learn more at xxiicentury.com, on Twitter @_xxiicentury, and on LinkedIn.

About KeyGene

KeyGene is a leading plant research company for higher crop yield and quality that revolutionized plant breeding using proprietary DNA technologies. Through the development and use of cutting-edge breeding technologies, bioinformatics, and data science expertise, KeyGene provides organizations with solutions to R&D challenges as well as plant-based trait platforms to deliver novel crop solutions. KeyGene was founded in 1989 and has locations in the Netherlands, United States, and India.

Learn more at keygene.com, on Twitter @KeyGeneInfo, and on LinkedIn.

Cautionary Note Regarding Forward-Looking Statements

Except for historical information, all of the statements, expectations, and assumptions contained in this press release are forward-looking statements. Forward-looking statements typically contain terms such as “anticipate,” “believe,” “consider,” “continue,” “could,” “estimate,” “expect,” “explore,” “foresee,” “goal,” “guidance,” “intend,” “likely,” “may,” “plan,” “potential,” “predict,” “preliminary,” “probable,” “project,” “promising,” “seek,” “should,” “will,” “would,” and similar expressions. Actual results might differ materially from those explicit or implicit in forward-looking statements. Important factors that could cause actual results to differ materially are set forth in “Risk Factors” in the Company’s Annual Report on Form 10-K filed on March 11, 2021. All information provided in this release is as of the date hereof, and the Company assumes no obligation to and does not intend to update these forward-looking statements, except as required by law.

Investor Relations & Media Contact:

Mei Kuo
Director, Communications & Investor Relations
22nd Century Group, Inc.
(716) 300-1221
[email protected]



First quarter of 2021: All business areas achieve sales and profit growth

PR Newswire

TOREKOV, Sweden, May 4, 2021 /PRNewswire/ —

  • Sales increased to SEK 2,645 million (2,065)
  • Operating profit (EBITA) rose to SEK 308 million (227)
  • EBITA margin of 11.6% (11.0)
  • Profit after tax was SEK 226 million (177)
  • Diluted earnings per share increased to SEK 8.43 (6.67)
  • Cash flow after investments amounted to SEK 71 million (–73)

“All business areas achieved good performance in the first quarter, with very strong growth in Medical Solutions and Integrated Solutions,” said Nolato President and CEO Christer Wahlquist. “Adjusted for currency and acquisitions, Group sales increased by a considerable 22%, and EBITA exceeded SEK 300 million for the first time in a single quarter.”

“This is once again a testament to our close customer relationships and our strong position as a global strategic partner for a raft of leading companies,” said Christer Wahlquist.

Medical Solutions sales for the quarter totaled SEK 1,006 million (642), corresponding to organic growth of a notable 17%. Operating profit (EBITA) rose by a remarkable 39% to SEK 121 million (87) and the EBITA margin was 12.0% (13.6).

“Growth was good in most areas, particularly in diagnostics, for which demand has increased partly because of the pandemic,” noted Christer Wahlquist. “The quarter also included a larger proportion of billing for development work and production equipment, which was around SEK 70 million higher than normal. The surgery segment continued to be negatively affected by the pandemic, particularly in the US business, but it showed an improvement towards the end of the quarter.”

“The strong growth in Medical Solutions has led us to recently take decisions to further expand our production capacity. In addition to the expansions we have already started in Switzerland, Hungary and Sweden, we will also be expanding the existing plants in Poland and the US.”

Integrated Solutions sales totaled SEK 1,045 million (854), corresponding to organic growth of an impressive 40%. Operating profit (EBITA) rose to SEK 125 million (111) and the EBITA margin was 12.0% (13.0).

“Sales were fueled by strong growth in Vaporiser Heating Products (VHP) and EMC,” said Christer Wahlquist. “In line with our previous assessment, VHP volumes ramped up in the quarter, while EMC benefited from both the 5G roll-out and our initiatives within Automotive. We expect VHP volumes to continue growing and sees sales for this business area increasing by around 15% in the second quarter compared with the first quarter of the year.”

Industrial Solutions sales totaled SEK 595 million (570), corresponding to organic growth of 1%. Operating profit (EBITA) rose by a remarkable 40% to SEK 66 million (47) and the EBITA margin was a strong 11.1% (8.2).

“There was a slightly negative impact from a components shortage in the automotive industry and effects of the pandemic in some areas,” added Christer Wahlquist. “However, our efficiency improvements have generated the desired effect, which is reflected by the sharp increase in earnings and the strong EBITA margin.”

For further information, please contact:

Christer Wahlquist, President and CEO, +46 (0)705 804848

Per-Ola Holmström, CFO, +46 (0)705 763340, [email protected]

Nolato is a Swedish group with operations in Europe, Asia and North America. We develop and manufacture products in polymer materials such as plastic, silicone and TPE for leading customers within medical technology, pharmaceuticals, consumer electronics, telecom, automotive, hygiene and other selected industrial sectors. Nolato’s shares are listed on Nasdaq Stockholm in the Large Cap segment, where they are included in the Industrials sector. www.nolato.com  

Prior to publication this information constituted inside information that Nolato AB is obliged to publish pursuant to the EU Market Abuse Regulation. This information is submitted through the agency of the above contact persons for publication on May 4, 2021 at 3.00 p.m. CET.

This information was brought to you by Cision http://news.cision.com

https://news.cision.com/nolato/r/first-quarter-of-2021–all-business-areas-achieve-sales-and-profit-growth,c3339712

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SOURCE Nolato

Arbill Offers Recommendations for HR Teams Eager to Protect Returning Employees

PHILADELPHIA, May 04, 2021 (GLOBE NEWSWIRE) — Companies are bringing employees back to the office, factory and/or facility through varying strategies₁:

  • Ford, with more than 30,000 U.S. employees working remotely, will transition to a “flexible hybrid work model” and will start this new approach in July.
  • IBM hasn’t set a specific timetable for asking workers to return to the office and expects about 80% of its 346,000 employees to return to a combination of remote and office schedules, determined by their roles.
  • Walmart’s approximately 15.1 million employees mostly work at its stores and many worked in-store throughout the pandemic. It plans to bring workers back to its Bentonville, Ark. campus no earlier than July.

As companies move forward with plans to bring employees back to work, HR teams and business owners will be responsible for ensuring that the workplace remains safe and employees are not subjected to an increased risk of contracting COVID-19. Arbill Industries, Inc. remains steadfast in its mission to educate employers and ensure that everyone returns home safely, every day.

“The safety needs of every company environment are different, even two offices that are of a similar size and configuration may have differing needs,” said Julie Copeland, CEO of Arbill, a U.S. and women-owned industrial safety company that has been providing personal protective equipment (PPE) to business and government agencies for more than 75 years. “In addition to understanding what specific PPE employees need, HR teams and employers must make certain they procure these products from companies with a reputation for high-quality and reliability.”

Masks are the first line of defense and despite their appearance, not all masks are alike. Arbill created its “Together” mask to meet the European Afnor standard, among the most stringent performance standards in the world.

The “Together” mask achieves 95% fabric filtration protection and is more breathable and comfortable than disposable medical masks. It remains 95% effective up to an average of 10-20 washes and remains 90% effective after 50 washes. With effectiveness lasting up to 50 washes, the masks’ cost per use averages eight cents, around 1/6 the cost of the cheapest disposable mask available at leading retail stores. The masks have also been treated with SILVADUR antimicrobial technology which inhibits the growth of microorganisms in the fabric. Masks are available to employees in a 6-pack or 12-pack, which will give employees enough product for every day of the week, including swapping in fresh products after lunch breaks.

In addition, because the Together mask is cotton, it biodegrades in approximately five months, versus 450 years for synthetic masks.

Arbill continues to look to medical and scientific professionals for guidance as products are continually tested and new consumer PPE products are developed.

For more information on “Together,” please visit HERE.


About Together

Launched in 2020 as a result of the COVID-19 pandemic, “Together” was founded by PPE manufacturing leader Arbill Industries. With more than 75 years of experience in protecting industry and government workers, Arbill understood a need for adequate protection for everyday people.

Born out of a timely need for a facial covering that offered unparalleled protection and all-day comfort, the industrial safety experts at Arbill engineered The Safety Mask℠. The first proprietary product in a forthcoming full line of consumer products that all start with an industrial safety standard. “Together” features professional-level protective apparel and accessories available to all.


About Arbill

As the leading provider of safety services, safety technology and safety products, Arbill is saving lives every day at industrial worksites throughout the United States. An award-winning supplier of all-things safety for more than 75 years, Arbill’s clients have counted on Arbill to make sure their employees go home safely after every shift. To assure our clients meet their safety goals, Arbill’s safety professionals are revolutionizing the way companies incorporate safety into their daily routines. Through Arbill’s comprehensive SafetyCare offering – Arbill provides more than 200,000 safety products (including nearly 1,000 items manufactured under Arbill’s highly-respected Truline brand), over 160 Environmental Health and Safety Training Courses and Safety Technologies that pull the entire offering together to create the best in safety. Arbill is a WBENC certified (women owned & certified business), ISO 9001 certified and FDA approved.

For more information about Arbill, visit: www.arbill.com


Media Contacts

Arbill

Sari Pollack
516.578.3381
[email protected]

UPRAISE Marketing + Public Relations

Tim Johnson / Madi Olivé / Victoria Cintra
[email protected]

The New York Times



Cobb County, Georgia, Selects Tyler Technologies for Commercial Privatization Appraisal Project

Cobb County, Georgia, Selects Tyler Technologies for Commercial Privatization Appraisal Project

County will also use Assessment Connect to better visualize property data

PLANO, Texas–(BUSINESS WIRE)–Tyler Technologies, Inc. (NYSE: TYL) announced today it has signed a five-year, $7.8 million agreement with the Cobb County Board of Tax Assessors in Georgia for Tyler’s CLT Appraisal Services and Assessment Connect solution. Tyler will be responsible for all phases of commercial property valuation in Cobb County, in addition to the implementation of Assessment Connect, a solution built on Tyler’s Socrata® open data platform that provides assessing offices with data access and analysis tools to help ensure fair and equitable property valuations.

As a long-standing client of Tyler, Cobb County already uses Tyler’s appraisal services to assist with residential property inspections and uses Tyler’s iasWorld® appraisal and tax administration software to manage assessment data. Tyler responded to Cobb County’s RFP for its commercial privatization appraisal project and was selected by the board of tax assessors.

“We are pleased to continue our great relationship with Tyler for this commercial privatization appraisal project,” said Stephen White, director and chief appraiser for Cobb County Tax Assessors. “We look forward to continuing work with Tyler to maintain fair market values for the county’s commercial properties, bringing equity to property owners. The addition of Assessment Connect will allow us to have an additional tool that will assist us in our valuation of many of the unique and complex properties in Cobb County.”

Tyler manages the valuation of all 13,800 commercial properties in Cobb County, representing more than $30 billion in value. The appraisal project also includes exempt properties such as schools, courthouses, utility, and other public buildings. Tyler’s dedicated team of 20 staff members support both the residential and commercial efforts. For residential, staff will conduct onsite data collection and verification of each property in the county; and for commercial properties, they will work to establish assessments based on the fair market value. Tyler will also manage the commercial appeals process with Cobb County once values are established.

Cobb County will also be using Tyler’s Assessment Connect solution – the first in Georgia to use this data solution. The county will be able to visualize data from its iasWorld solution to help identify trends in both residential and commercial properties. Assessment Connect will provide county assessors with real-time data and insights into appraisals, appeals, and property development efforts.

“We’ve been able to improve the appraisal process for Cobb County through prior property assessment projects, and we’re pleased to have the opportunity to continue doing so for the county’s commercial properties,” said Jake Wilson, senior vice president and general manager of appraisal services for Tyler. “We’re equally excited to introduce Assessment Connect to our first county in Georgia. We believe it will bring valuable insights around property trends to Cobb County immediately upon implementation and for many years to come.”

Cobb County is located in the Atlanta metropolitan area. It has a population of roughly 760,000, making it Georgia’s third most-populous county. Tyler also provides its EnerGov civic services solution to the county and its Munis® enterprise resource planning solution to Cobb County School District. In addition to Cobb County, Tyler also currently provides appraisal services to the counties of DeKalb, Fulton, Gwinnett, and Clayton in the Atlanta area.

About Tyler Technologies, Inc.

Tyler Technologies (NYSE: TYL) provides integrated software and technology services to the public sector. Tyler’s end-to-end solutions empower local, state, and federal government entities to operate more efficiently and connect more transparently with their constituents and with each other. By connecting data and processes across disparate systems, Tyler’s solutions are transforming how clients gain actionable insights that solve problems in their communities. Tyler has more than 27,000 successful installations across more than 11,000 sites, with clients in all 50 states, Canada, the Caribbean, Australia, and other international locations. Tyler has been named to Government Technology’s GovTech 100 list five times and has been recognized three times on Forbes’ “Most Innovative Growth Companies” list. More information about Tyler Technologies, an S&P 500 company headquartered in Plano, Texas, can be found at tylertech.com.

Jennifer Kepler

Tyler Technologies

972.713.3770

[email protected]

KEYWORDS: United States North America Texas Georgia

INDUSTRY KEYWORDS: Commercial Building & Real Estate Software Construction & Property Data Management Accounting Professional Services Technology Residential Building & Real Estate

MEDIA:

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MIMEDX Urges Shareholders to Consider Prescience Point’s Motivations Before Voting Their Shares at the Company’s Annual Meeting

Questions Every Shareholder Should Ask Prescience Point

Prescience Point’s Trading History Tells the Real Story

MARIETTA, Ga., May 04, 2021 (GLOBE NEWSWIRE) — MIMEDX Group, Inc. (NASDAQ: MDXG) (“MIMEDX” or the “Company”), an industry leader in utilizing amniotic tissue as a platform for regenerative medicine, today urged shareholders to consider several key questions about Prescience Point’s interests, motivations and actions regarding the disruptive proxy fight it is waging to gain undue influence over the MIMEDX Board of Directors. MIMEDX believes shareholders deserve to have the facts before voting their shares at the Company’s 2021 Annual Meeting of Shareholders (“Annual Meeting”).

Before voting their shares, MIMEDX shareholders should consider what motivations truly drive Prescience Point’s campaign.

THE QUESTIONS:

1. Is it ethical or appropriate to buy shares, publish a promotional “report” hyping a nearly $32 price target, and quickly sell shares for a profit when the stock price rises after the “report” is disseminated?

  • Prescience Point bought shares before it issued its December 2020 “report,”

    1

    then quickly flipped an equivalent amount of shares following the stock rise that occurred after issuing its “report.”

2. Is Prescience Point acting on behalf of all MIMEDX shareholders or only its own interests?

3. Why is Prescience Point seeking to replace its OWN director nominees, appointed just two years ago — Board Chair, Dr. M. Kathleen Behrens and Audit Committee Chair, K. Todd Newton – both of whom Prescience Point itself said add value to the Board in view of their “immense credibility and reputational capital”, are “world-class” and would “bring value to all shareholders”?2 Why does Prescience Point now seek to oust its OWN director nominees who have been outstanding leaders on the Board?

4. What is Prescience Point’s shelf life for director designees? Less than two years?

5. Why has Prescience Point nominated candidates with no or very little public company board experience?

6. Why did Prescience Point turn down our settlement offer that addressed its demand for board representation and additional investment by the Company in our shareholder communications program?

7. Is Prescience Point actually seeking control when it seeks to replace the board seats of key board leaders – Chair, CEO, and Audit Committee Chair?

8. Is Prescience Point just pushing for a fire-sale of the Company because their fund is so heavily invested in MIMEDX?

  • Prescience Point’s portfolio is extremely concentrated in MDXG – more than 73% of its estimated assets under management (AUM) as of December 31, 2020 are invested in MDXG.

9. What are Prescience Point’s motivations behind pursuing a quick sale, at this stage in the Company’s clinical trial pipeline?

  • It is more likely shareholders capture substantially greater value through a transaction after a company has clinical data results in a U.S. Food & Drug Administration (FDA) approved treatment for indications which command a sizeable market with commercialization plans underway.

10. Why would Prescience Point push a company to take overly-aggressive positions regarding our products that may be counter to FDA best practices – especially now, when the Company has finally restored its credibility with both the FDA and Securities and Exchange Commission (SEC)?




THE FACTS

Publicly reported trading activity shows that Prescience Point has generated short-term trading profits driven by its promotional, self-publication, of a “report” with lofty share price targets:

  • Prescience Point purchased approximately 200,697 shares of MIMEDX common stock between December 08, 2020 and December 10, 2020.3 They admit this in their January 13, 2021 Schedule 13D filing with the SEC.
  • On December 16, 2020, Prescience Point authored and self-published an opinion piece4 stylized to resemble the professional, digital packaging of a sell-side analyst report issued by a prominent Wall Street firm. In their “report”, Prescience Point commends MIMEDX’s turnaround success, leadership team and the “blockbuster, game-changing” potential of AMNIOFIX for the treatment of knee osteoarthritis, disclosing a stock price target of nearly $32.
  • MIMEDX’s share price at the time of the Prescience Point promotional “report” was $6.58.
  • Within two days of releasing its “report,” Prescience Point opportunistically sold 214,597 shares of MIMEDX’s common stock, at prices ranging from $8.12 to $9.61, despite having a target price of nearly $32. These price points represent a premium range of 23% to 46% over the Company’s closing stock price on the trading day immediately prior to the self-publication of Prescience Point’s “report.” (See chart. https://www.globenewswire.com/NewsRoom/AttachmentNg/22300c39-ca08-4222-91df-569e53ae8c30)

In its Proxy statement, Prescience Point takes credit for the stock price increase following the publication of its promotional “report” but neglects to disclose its subsequent stock sales at a higher price. 5

Do not allow Prescience Point to put your investment at risk by giving them further and undeserved influence over the Board and therefore, the business of MIMEDX. Prescience Point’s demands and commentary indicate that they do not understand responsible or compliant public pharmaceutical company disclosure, and instead are advocating for speculative actions designed to satisfy their own agenda.

The MIMEDX Board and management team have the opportunity to continue the successful execution of the Company’s clear strategic plan to accelerate its late-stage pipeline, achieve its stated top-line growth objectives in its core business and drive shareholder value.

The Company’s Board of Directors and management team have taken decisive and positive actions to create shareholder value by restoring the Company’s integrity, improving business liquidity, and transforming the culture of the organization. MIMEDX stock has appreciated 237% since the Company appointed Timothy R. Wright as CEO in May of 2019.

Today, MIMEDX is a much stronger company that is very well-positioned to capitalize on the growing opportunities in the regenerative medicine industry.

Our transformation is not complete. MIMEDX’s future success is dependent on continuing to execute and operate our business in a compliant and transparent manner. Any action that puts this approach at risk puts the Company’s progress, and the future of its shareholders’ investment, at risk.

The MIMEDX Board of Directors unanimously recommends that shareholders vote the WHITE proxy card FOR MIMEDX’s four highly qualified directors standing for election – Dr. M. Kathleen Behrens, Mr. Todd Newton, Mr. Timothy R. Wright, and Dr. Phyllis Gardner.

PROTECT YOUR INVESTMENT! VOTE THE WHITE PROXY CARD TODAY “FOR ALL” FOUR OF MIMEDX’S HIGHLY QUALIFIED DIRECTOR NOMINEES


Your Vote Is Important, No Matter How Many

or How Few Shares You Own
 
You can vote by Internet, telephone or by signing and dating the WHITE proxy card and mailing it in the envelope provided.
 
If you have any questions about how to vote your shares, or need additional assistance, please contact:
 
MORROW
SODALI
 
[email protected] 
(203) 658-9400
or

Toll-Free (800) 662-5200

 

MIMEDX will be holding its Annual Meeting virtually on May 27, 2021 at 10:00 a.m. Eastern Time at www.cesonlineservices.com/mdxg21_vm. MIMEDX shareholders of record as of 5:00 p.m. Eastern Time on April 16, 2021 are entitled to vote at the Annual Meeting.

MIMEDX’s definitive proxy materials, letter to shareholders and other relevant information can be found at https://votemimedx.com/.

Important Cautionary Statement

This communication contains forward-looking statements, including, among other things, statements regarding: (i) our strategic plan, as illustrated by our current business priorities, and our ability to implement these priorities; (ii) our expectations regarding the sufficiency of our liquidity and existing capital resources to implement our current business priorities; (iii) the advantages of our products and development of new products; (iv) our expectation regarding the size of the potential market and any growth in such market; (v) the likelihood, timing, and scope of possible regulatory approval and commercial launch of our late-stage product candidates and new indications for our products; (vi) the status, timing, and expected results of the Company’s clinical trials and planned regulatory submissions, and our expectations regarding our ability to potentially accelerate the timing of any trial or regulatory submission; (vii) our ability to transform the Company’s culture while maintaining its integrity; (viii) the effectiveness of amniotic tissue as a therapy for any particular indication or condition; (ix) estimates of potential addressable markets for our potential future products; and (x) our expectations regarding the effects of the proxy contest launched by Prescience Point. Additional forward-looking statements may be identified by words such as “believe,” “expect,” “may,” “plan,” “goal,” “outlook,” “potential,” “will,” “preliminary,” and similar expressions, and are based on management’s current beliefs and expectations.

Forward-looking statements are subject to risks and uncertainties, and the Company cautions investors against placing undue reliance on such statements. Actual results may differ materially from those set forth in the forward-looking statements. Factors that could cause actual results to differ from expectations include: (i) notwithstanding the FDA’s statement on April 21, 2021, there remain a number of uncertainties regarding the application of the FDA’s regulations to the Company’s products and practices, and the Company may adjust its plans to comply with FDA’s requirements; (ii) there can be no assurance that the FDA will further extend enforcement discretion to cover products that have a regulatory approval pending, nor can there be any assurance that the Company will even be able to engage with the FDA on the subject; (iii) the Company’s estimate of the impact of enforcement discretion assumes that the Company is able to sell its products through May 31, 2021, and that the Company may continue to sell its cord products thereafter; (iv) the status, timing, and expected results of the Company’s clinical trials and planned regulatory submissions, and our expectations regarding our ability to potentially accelerate the timing of any trial or regulatory submission depend on a number of factors including favorable trial results, patient access, and our ability to manufacture in accordance with CGMP and appropriate chemistry and manufacturing controls; (v) the Company may change its plans due to unforeseen circumstances, and delay or alter the timeline for future trials, analyses, or public announcements; (vi) generally any meeting with the FDA depends on successful clinical trial results and the availability of such a meeting and its timing is outside of the Company’s control; (vii) the results of a clinical trial or trials may have little or no statistical value, or may fail to demonstrate that the product is safe or effective; (viii) our estimates of potential addressable markets for our potential future products are merely estimates and will depend on market acceptance of our potential, future products; (ix) we depend on our senior leadership team and may not be able to retain or replace these employees or recruit additional qualified personnel; and (x) actions that Prescience Point may take in connection with the proxy contest, which are outside our control. The Company describes additional risks and uncertainties in the Risk Factors section of its most recent annual report and quarterly reports filed with the SEC. Any forward-looking statements speak only as of the date of this communication and the Company assumes no obligation to update any forward-looking statement.

Important Information

The Company, its directors, director nominees and certain of its executive officers are participants in the solicitation of proxies from shareholders in respect of the Annual Meeting. The Company has filed a definitive proxy statement and associated WHITE proxy card in connection with the solicitation of proxies for the Annual Meeting with the SEC. Details concerning the nominees of the Company’s board of directors for election at the Annual Meeting are set forth in the definitive proxy statement. BEFORE MAKING ANY VOTING DECISION, SHAREHOLDERS OF THE COMPANY ARE URGED TO READ ALL RELEVANT DOCUMENTS FILED WITH OR FURNISHED TO THE SEC, INCLUDING THE COMPANY’S DEFINITIVE PROXY STATEMENT AND ANY SUPPLEMENTS THERETO, AS THEY CONTAIN IMPORTANT INFORMATION. Information regarding the identity of the Company’s participants and their respective interests in the matters to be voted on at the Annual Meeting, by security holdings or otherwise, are set forth in the definitive proxy statement and other documents filed with the SEC in connection with the Annual Meeting. Investors and shareholders can obtain a copy of the definitive proxy statement and other documents filed by the Company free of charge from the SEC’s website at www.sec.gov. The Company’s shareholders can also obtain, without charge, a copy of the definitive proxy statement and other relevant filed documents from the “SEC Filings” section of the Company’s website at www.mimedx.com.

About MIMEDX

MIMEDX is an industry leader in utilizing amniotic tissue as a platform for regenerative medicine, developing and distributing placental tissue allografts with patent-protected, proprietary processes for multiple sectors of healthcare. As a pioneer in placental biologics, we have both a core business, focused on addressing the needs of patients with acute and chronic non-healing wounds, and a promising late-stage pipeline targeted at decreasing pain and improving function for patients with degenerative musculoskeletal conditions. We derive our products from human placental tissues and process these tissues using our proprietary methods, including the PURION® process. We employ Current Good Tissue Practices, Current Good Manufacturing Practices, and terminal sterilization to produce our allografts. MIMEDX has supplied over two million allografts, through both direct and consignment shipments. For additional information, please visit www.mimedx.com.

Contacts:

Investors:

Jack Howarth
Investor Relations
404-360-5681
[email protected]   

Media:

Hilary Dixon
Corporate Communications
770-651-9307
[email protected]


1
https://www.presciencepoint.com/wp-content/uploads/2020/12/MDXG-Amniofix-Report-FINAL.pdf

2 Prescience Schedule 13D/A, filed with the SEC on May 8, 2019
3https://www.sec.gov/Archives/edgar/data/0001765316/000101143821000032/form_sc13d-mimedx.htm
4https://www.presciencepoint.com/wp-content/uploads/2020/12/MDXG-Amniofix-Report-FINAL.pdf
5 Prescience Schedule 14A, page 4, filed with the SEC on May 03, 2021.



Elbit Systems of America and Textron Systems team on Advanced Reconnaissance Vehicle prototype for USMC

PR Newswire

FORT WORTH, Texas, May 4, 2021 /PRNewswire/ — As the United States Marine Corps (USMC) Systems Command works toward the next phase of replacing the legacy Light Armored Vehicle with a modern, robust Advanced Reconnaissance Vehicle (ARV), Elbit Systems of America has teamed with Textron Systems to produce a solution that provides Marines with transformational capabilities, including enhanced situational understanding technologies.

The USMC has identified characteristics their new ARV must include as the core-manned next-generation system for light armored reconnaissance battalions. In response, Textron Systems has partnered with Elbit Systems of America and others to create the Cottonmouth prototype ARV.

“Elbit Systems of America is excited to be teamed with Textron Systems as a key partner for building the Advanced Reconnaissance Vehicle for the United States Marine Corps,” said Ridge Sower, Vice President of Ground Combat and Precision Targeting at Elbit Systems of America. “Our ARV concept will provide a key and critical capability to the USMC and include advanced technologies that will make it relevant both today and for decades to come. Our 360-degree multi-domain situational awareness suite will provide significant increases in the lethality and survivability of Marines.”

Building off the success of Elbit Systems of America’s IronVision and gimbaled sight solutions, the company will provide the 360° Situational Awareness vision suite for the Cottonmouth prototype ARV. The system will bring together video images from outside the ARV, overlay terrain and obstacle information, along with navigation and battlespace symbology, and present a single image of the ARV’s surroundings to all crew members within the vehicle. This comprehensive and intuitive view of their surroundings, available both on crew workstations and the IronVision Helmet Mounted Display, gives the crew the ability to “see-through” the armor of the Cottonmouth, empowering them with unparalleled situational understanding while under armor.

The successful ARV prototype will ultimately replace the USMC’s Light Armored Vehicle that’s been in use since the 1980s.

More information:

About Elbit Systems of America, LLC

Elbit Systems of America, headquartered in Fort Worth, Texas, is a leading provider of high-performance products, system solutions, and support services focusing on the defense, homeland security, law enforcement, commercial aviation, and medical instrumentation markets. With facilities throughout the U.S., Elbit Systems of America is dedicated to supporting those who contribute daily to the safety and security of the United States. Elbit Systems of America, LLC is wholly owned by Elbit Systems Ltd. (NASDAQ: ESLT and TASE: ESLT), a global high technology company engaged in a wide range of programs for innovative defense and commercial applications. For additional information, visit: www.ElbitAmerica.com or follow us on Twitter, LinkedIn and Instagram.

About Elbit Systems

Elbit Systems Ltd. is an international high technology company engaged in a wide range of defense, homeland security and commercial programs throughout the world. The Company, which includes Elbit Systems and its subsidiaries, operates in the areas of aerospace, land and naval systems, command, control, communications, computers, intelligence surveillance and reconnaissance (“C4ISR”), unmanned aircraft systems, advanced electro-optics, electro-optic space systems, EW suites, signal intelligence systems, data links and communications systems, radios, cyber-based systems and munitions. The Company also focuses on the upgrading of existing platforms, developing new technologies for defense, homeland security and commercial applications and providing a range of support services, including training and simulation systems. For additional information, visit: https://elbitsystems.com/, follow us on Twitter or visit our official Facebook, YouTube and LinkedIn Channels.

Trademarks

Elbit Systems of America and other trademarks, service marks and logos are registered or unregistered marks of Elbit Systems of America companies in the United States and in foreign countries. Copyright ©2021Elbit Systems of America. All rights reserved.

Forward Looking Statement

This press release may contain forward–looking statements (within the meaning of Section 27A of the Securities Act of 1933, as amended, Section 21E of the Securities Exchange Act of 1934, as amended and the Israeli Securities Law, 1968) regarding Elbit Systems Ltd. and/or its subsidiaries (collectively the Company), to the extent such statements do not relate to historical or current facts. Forward-looking statements are based on management’s current expectations, estimates, projections and assumptions about future events. Forward–looking statements are made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995, as amended. These statements are not guarantees of future performance and involve certain risks, uncertainties and assumptions about the Company, which are difficult to predict, including projections of the Company’s future financial results, its anticipated growth strategies and anticipated trends in its business.  Therefore, actual future results, performance and trends may differ materially from these forward–looking statements due to a variety of factors, including, without limitation: scope and length of customer contracts; governmental regulations and approvals; changes in governmental budgeting priorities; general market, political and economic conditions in the countries in which the Company operates or sells, including Israel and the United States among others; changes in global health and macro-economic conditions; differences in anticipated and actual program performance, including the ability to perform under long-term fixed-price contracts; changes in the competitive environment; and the outcome of legal and/or regulatory proceedings.  The factors listed above are not all-inclusive, and further information is contained in Elbit Systems Ltd.’s latest annual report on Form 20-F, which is on file with the U.S. Securities and Exchange Commission. All forward–looking statements speak only as of the date of this release. Although the Company believes the expectations reflected in the forward-looking statements contained herein are reasonable, it cannot guarantee future results, level of activity, performance or achievements. Moreover, neither the Company nor any other person assumes responsibility for the accuracy and completeness of any of these forward-looking statements. The Company does not undertake to update its forward-looking statements.

Elbit Systems Ltd., its logo, brand, product, service and process names appearing in this Press Release are the trademarks or service marks of Elbit Systems Ltd. or its affiliated companies.  All other brand, product, service and process names appearing are the trademarks of their respective holders.  Reference to or use of a product, service or process other than those of Elbit Systems Ltd. does not imply recommendation, approval, affiliation or sponsorship of that product, service or process by Elbit Systems Ltd. Nothing contained herein shall be construed as conferring by implication, estoppel or otherwise any license or right under any patent, copyright, trademark or other intellectual property right of Elbit Systems Ltd. or any third party, except as expressly granted herein.

Media Contacts:

Greg Caires | 682-286-2299 | [email protected]

Amy Hartley I 682-286-2411 I [email protected]

 

Cision View original content to download multimedia:http://www.prnewswire.com/news-releases/elbit-systems-of-america-and-textron-systems-team-on-advanced-reconnaissance-vehicle-prototype-for-usmc-301282840.html

SOURCE Elbit Systems of America, LLC

Citius Pharmaceuticals to Present Mino-Lok® and COVID-related Respiratory Treatment Update at Benzinga Global Small Cap Conference on Thursday, May 13

Citius to highlight corporate strategy and pipeline progress

Citius advances Mino-Lok®, an antibiotic lock solution for the treatment of catheter-related bloodstream infections, through a Phase 3 pivotal superiority clinical trial

Preclinical activities underway for Citius’s unique, proprietary stem cell therapy for Acute Respiratory Distress Syndrome (ARDS) associated with COVID-19

PR Newswire

CRANFORD, N.J., May 4, 2021 /PRNewswire/ — Citius Pharmaceuticals, Inc. (“Citius” or the “Company”) (Nasdaq: CTXR), a specialty pharmaceutical company dedicated to the development and commercialization of critical care products with a focus on anti-infective products in adjunct cancer care, unique prescription products and stem cell therapy, today announced that it will participate in the virtual Benzinga Global Small Cap Conference being held May 13-14, 2021.

Citius President and Chief Executive Officer Myron Holubiak will present at 1:50 p.m. ET on Thursday, May 13. Investors may register for the conference at the event website, and Mr. Holubiak’s presentation may be viewed live on the Benzinga YouTube channel.

During his presentation, Mr. Holubiak will focus on the Company’s pipeline strategy and highlight Citius’s novel stem-cell program for the treatment of Acute Respiratory Distress Syndrome (ARDS), a life-threatening condition, and the most common cause of respiratory failure and death in COVID-19 patients. Currently, there is no FDA-approved drug therapy available for ARDS.

About Citius Pharmaceuticals, Inc.
Citius is a late-stage specialty pharmaceutical company dedicated to the development and commercialization of critical care products, with a focus on anti-infectives in adjunct cancer care, unique prescription products, and stem cell therapy. The Company’s lead product candidate, Mino-Lok®, an antibiotic lock solution for the treatment of patients with catheter-related bloodstream infections (CRBSIs), is currently enrolling patients in a Phase 3 pivotal superiority trial.  Mino-Lok® was granted Fast Track designation by the U.S. Food and Drug Administration (FDA). Through its subsidiary, NoveCite, Inc., Citius is developing a novel proprietary stem cell treatment derived from induced pluripotent stem cells (iPSCs) for acute respiratory conditions, with a near-term focus on Acute Respiratory Distress Syndrome (ARDS) associated with COVID-19.  For more information, please visit www.citiuspharma.com.

Investor Relations for Citius Pharmaceuticals:

Andrew Scott

Vice President, Special Projects
T: 908-967-6677 x105
E: [email protected]

Ilanit Allen

T: 908-967-6677 x113
E: [email protected]

Cision View original content:http://www.prnewswire.com/news-releases/citius-pharmaceuticals-to-present-mino-lok-and-covid-related-respiratory-treatment-update-at-benzinga-global-small-cap-conference-on-thursday-may-13-301283314.html

SOURCE Citius Pharmaceuticals, Inc.