Greenwich LifeSciences, Inc. Announces Partnership with Baylor College of Medicine for its Planned Phase III Clinical Trial

Greenwich LifeSciences, Inc. Announces Partnership with Baylor College of Medicine for its Planned Phase III Clinical Trial

STAFFORD, Texas–(BUSINESS WIRE)–
Greenwich LifeSciences, Inc. (Nasdaq: GLSI) (the “Company”), a clinical-stage biopharmaceutical company focused on the development of GP2, an immunotherapy to prevent breast cancer recurrences in patients who have previously undergone surgery, today announced the formation of a partnership with Baylor College of Medicine in Houston, Texas to act as the lead clinical site for the Company’s upcoming Phase III clinical trial. Professor Mothaffar F. Rimawi has agreed to serve as the Global Principal Investigator of the Phase III clinical trial, and Professor C. Kent Osborne and Professor Rimawi are expected to serve as the first members of the Company’s Clinical Advisory Board for the development of GP2 immunotherapy across all indications and HER2 expressing cancers.

Snehal Patel, CEO of Greenwich LifeSciences, commented, “We are pleased to have entered into this collaboration with such prominent key opinion leaders who are truly committed to evaluating the potential of GP2 immunotherapy. Due to GP2’s safety profile, GP2 immunotherapy may provide clinicians with an option to deescalate treatment of patients by reducing the use of other, more toxic and expensive standard of care treatments. Both Professors Rimawi and Osborne have already introduced us to other breast cancer clinical sites and clinical leaders who have provided input into the design of the upcoming Phase III trial and who have expressed an interest in participating in the Phase III trial as high enrollment sites. In addition, we have also been jointly exploring the addition of both US and European breast cancer cooperative groups to more rapidly expand the clinical team.”

Professor Rimawi added, “We are excited to jointly evaluate the potential of GP2 immunotherapy. We believe that our patients will seek to participate in the upcoming trial as the GP2 Phase IIb clinical trial data suggests that GP2 could be both safe and effective and could be easily administered during standard of care follow-up visits. Our patients are seeking safe preventative treatments that allow them to transition away from the trauma of surgery, trastuzumab-based therapies, other HER2 targeted therapies, chemotherapy, and radiation as they seek to return to normal and healthy lives.”

Professor Osborne commented, “Bringing new alternatives to chemotherapy and improving quality of life for patients undergoing treatment for breast cancer are primary focuses of the Breast Cancer Program. GP2 immunotherapy may represent one such opportunity, and we look forward to collaborating with Greenwich LifeSciences and supporting the planned clinical trial with the resources of both the Dan L Duncan Comprehensive Cancer Center and the Baylor College of Medicine.”

Professor Mothaffar F. Rimawi is board certified in internal medicine, hematology and medical oncology, and serves as both Executive Medical Director and Co-Leader of the Breast Cancer Program at the Dan L Duncan Comprehensive Cancer Center.

Professor C. Kent Osborne is board certified in internal medicine, hematology and medical oncology, and serves as both the Tina and Dudley Sharp Chair in Oncology and the founding Director of the Dan L Duncan Comprehensive Cancer Center. Professor Osborne is also Professor of Medicine and Molecular and Cellular Biology at Baylor College of Medicine.

About Dan L Duncan Comprehensive Cancer Center

The Dan L Duncan Comprehensive Cancer Center at Baylor College of Medicine has grown and matured over the 13 years since its original designation as a Cancer Center by the National Cancer Institute, which was followed by an NCI Comprehensive Cancer Center designation in 2015. The clinical operations have expanded with new faculty and programs, and the center moved into new clinical space on the McNair campus in January 2019. The research portfolio has grown dramatically to more than $180 million in annual cancer relevant research funding today from less than $100 million in 2007. These amazing accomplishments were made possible by the transformational gift in 2006 from Dan L Duncan and his family.

Baylor College of Medicine

Baylor College of Medicine is a leading health sciences university that creates knowledge and applies science and discoveries to further education, healthcare and community service locally and globally. The College was founded in the early 1900s, and in 1943, the MD Anderson Foundation invited Baylor University College of Medicine to join the newly formed Texas Medical Center in Houston, Texas. Four years later, the College moved into its present site in The Roy and Lillie Cullen Building, the first building completed in the new Texas Medical Center. The College’s rise in prominence began in the 1950s when Dr. Michael E. DeBakey’s innovative surgical techniques garnered international attention. In 1969, the College separated from Baylor University to become an independent institution.

About Breast Cancer and HER2/neu Positivity

One in eight U.S. women will develop invasive breast cancer over her lifetime, with approximately 266,000 new breast cancer patients and 3.1 million breast cancer survivors in 2018. HER2/neu (human epidermal growth factor receptor 2) protein is a cell surface receptor protein that is expressed in a variety of common cancers, including in 75% of breast cancers at low (1+), intermediate (2+), and high (3+ or over-expressor) levels.

About Greenwich LifeSciences, Inc.

Greenwich LifeSciences is a clinical-stage biopharmaceutical company focused on the development of GP2, an immunotherapy to prevent breast cancer recurrences in patients who have previously undergone surgery. GP2 is a 9 amino acid transmembrane peptide of the HER2/neu protein. In a randomized, single-blinded, placebo-controlled, multi-center (16 sites led by MD Anderson Cancer Center) Phase IIb clinical trial, no recurrences were observed in the HER2/neu 3+ adjuvant setting after median 5 years of follow-up, if the patient received the 6 primary intradermal injections over the first 6 months (p = 0.0338). Of the 138 patients that have been treated with GP2 to date over 4 clinical trials, GP2 treatment was well tolerated and no serious adverse events were observed related to GP2 immunotherapy. Greenwich LifeSciences is planning to commence a Phase III clinical trial using a similar treatment regime as the Phase IIb clinical trial. For more information on Greenwich LifeSciences, please visit the company’s website: www.greenwichlifesciences.com

Forward-Looking Statement Disclaimer

Statements in this press release contain “forward-looking statements” that are subject to substantial risks and uncertainties. All statements, other than statements of historical fact, contained in this press release are forward-looking statements. Forward-looking statements contained in this press release may be identified by the use of words such as “anticipate,” “believe,” “contemplate,” “could,” “estimate,” “expect,” “intend,” “seek,” “may,” “might,” “plan,” “potential,” “predict,” “project,” “target,” “aim,” “should,” “will” “would,” or the negative of these words or other similar expressions, although not all forward-looking statements contain these words. Forward-looking statements are based on Greenwich LifeSciences Inc.’s current expectations and are subject to inherent uncertainties, risks and assumptions that are difficult to predict. Further, certain forward-looking statements are based on assumptions as to future events that may not prove to be accurate. These and other risks and uncertainties are described more fully in the section titled “Risk Factors” in the final prospectus related to the public offering filed with the Securities and Exchange Commission. Forward-looking statements contained in this announcement are made as of this date, and Greenwich LifeSciences Inc. undertakes no duty to update such information except as required under applicable law.

Investor & Public Relations Team

Snehal Patel

Investor Relations

(832) 819-3232

[email protected]

KEYWORDS: United States North America Texas

INDUSTRY KEYWORDS: Oncology Education Health Hospitals Clinical Trials University Biotechnology

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SYKES Announces Launch of SYKES Digital Services Division

SYKES Announces Launch of SYKES Digital Services Division

SYKES Digital Services (SDS) consolidates capabilities spanning automation, self-service, insight analytics, and digital learning to transform the customer experience

TAMPA, Fla.–(BUSINESS WIRE)–Sykes Enterprises, Incorporated (“SYKES” or the “Company”) (NASDAQ: SYKE), a leading full life cycle provider of global customer engagement services, multichannel demand generation, and digital transformation, today announced the launch of SYKES Digital Services (https://www.sykes.com/digital/).

This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20201112005155/en/

SYKES Digital Services (Graphic: Business Wire)

SYKES Digital Services (Graphic: Business Wire)

Over the past decade, SYKES’ acquisition of market-leading digital capabilities in combination with core business process expertise has established it as a true customer experience management powerhouse. SYKES Digital Services (SDS) consolidates capabilities spanning automation, self-service, insight analytics, and digital learning to reimagine the future of work. With a strategic focus on transforming the customer experience, SYKES enables clients to outpace disruption, and win in a digital world.

The launch of SYKES Digital Services comes at a critical time when businesses across the globe are facing an onslaught of new challenges and are increasingly focused on remaining competitive in a rapidly evolving landscape.

With proven expertise in optimizing customer experience, and a heritage of excellenceacross all disciplines, SYKES Digital Services is uniquely positioned to deliver solutions that supercharge workforces, reduce operating costs, improve customer experience, and unlock growth with a holistic approach that encompasses:

  • SYKES’ tradition of delivering world-class customer experiences while exploring opportunities for continuous improvement and operational innovation.
  • Symphony Ventures’ pedigree in deploying RPA and Intelligent Automation with unrivalled execution and accountability to transform processes with certainty of outcome.
  • Qelp’s expertise in serving customers on their preferred self-service channels, providing efficient and effective customer support experiences.
  • TalentSprout’s legacy of engaging and supporting employees through fundamental changes in the workplace along with essential work-at-home support and training.
  • SYKES Insight Analytics’ award winning CX analytics solution enabling the collation of disparate, unstructured data to effectively connect the dots, gain efficiencies and ultimately increase the lifetime value of customers.

Many leading organizations are citing intelligent automation and robust digital strategies as being key to increased agility and resiliency now and for years to come. The integrated, yet nimble structure of SDS will allow us to anticipate and meet the needs of its clients with a firm commitment to operational excellence through a focused and programmatic approach to digital transformation.

“For over 40 years, outpacing disruption to better serve the customer has been at the heart of everything we do. Thanks to our vision and targeted investments in market-leading digital capabilities, we believe SYKES Digital Services is uniquely positioned as the transformation partner of choice for enterprises looking to create more meaningful and impactful intelligent customer experiences,” said Chuck Sykes, President & CEO at SYKES.

“The SYKES Digital Services division is the culmination of careful thought and consideration of how to best align the capabilities amassed through SYKES’ strategic acquisition strategy to continue delivering upon our unique mission of helping consumers find and use the product and services they need by combining the power of machine intelligence and human ingenuity. I am honored to lead this team of dedicated and talented individuals,” said David Brain, Chief Digital Officer at SYKES.

For more information, please visit https://www.sykes.com/digital/.

About Sykes Enterprises, Incorporated

Sykes Enterprises, Incorporated (“SYKES” or “the Company”) is a leading provider of multi-channel demand generation and global customer engagement services. The Company provides differentiated full lifecycle customer engagement solutions and services primarily to Global 2000 companies and their end customers principally in the financial services, communications, technology, transportation & leisure and healthcare industries. SYKES’ differentiated full lifecycle management services platform effectively engages customers at every touchpoint within the customer journey, including digital marketing and acquisition, sales expertise, customer service, technical support and retention, many of which can be optimized by a suite of robotic process automation (“RPA”) and artificial intelligence (“AI”) solutions. The Company serves its clients through two geographic operating regions: the Americas (United States, Canada, Latin America, South Asia and Asia Pacific) and EMEA (Europe, the Middle East and Africa). Its Americas and EMEA regions primarily provide customer-engagement solutions and services with an emphasis on inbound multichannel demand generation, customer service and technical support to its clients’ customers. These services are delivered through multiple communication channels including phone, email, social media, text messaging, chat and digital self-service. The Company also provides various enterprise support services in the United States that include services for its clients’ internal support operations, from technical staffing services to outsourced corporate help desk services. In Europe, the Company provides fulfillment services, which includes order processing, payment processing, inventory control, product delivery and product returns handling. Additionally, through the acquisition of RPA provider Symphony Ventures Ltd (“Symphony”) coupled with its investment in AI through XSell Technologies, Inc. (“XSell”), the Company also provides a suite of solutions such as consulting, implementation, hosting and managed services that optimizes its differentiated full lifecycle management services platform. SYKES’ complete service offering helps its clients acquire, retain and increase the lifetime value of their customer relationships. The Company has developed an extensive global reach with customer engagement centers across six continents, including North America, South America, Europe, Asia, Australia and Africa. It delivers cost-effective solutions that generate demand, enhance the customer service experience, promote stronger brand loyalty, and bring about high levels of performance and profitability. For additional information please visit www.sykes.com.

Jesse Himsworth

Senior Vice President, Global Marketing

Sykes Enterprises, Incorporated

[email protected]

801-874-9390

Subhaash Kumar

Global VP of Finance & Investor Relations

Sykes Enterprises, Incorporated

[email protected]

813-233-7143

KEYWORDS: United States North America Florida

INDUSTRY KEYWORDS: Technology Human Resources Other Communications Consulting Marketing Communications Professional Services Software Data Management

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SYKES Digital Services (Graphic: Business Wire)

Amazon In-Garage Delivery Expands to Millions More Prime Members in Over 4,000 Cities

Amazon In-Garage Delivery Expands to Millions More Prime Members in Over 4,000 Cities

Originally launched in 50 cities, Key by Amazon’s secure, convenient, and contactless In-Garage Delivery service is expanding to tens of millions of Prime members in over 4,000 cities across the U.S.

Key by Amazon is also launching Key In-Garage Grocery Delivery, allowing eligible Prime members to have grocery orders from Whole Foods Market or Amazon Fresh delivered securely inside their garage

SEATTLE–(BUSINESS WIRE)–
(NASDAQ:AMZN)— Today, Amazon announced that tens of millions of Amazon Prime members will now have access to Key by Amazon’s In-Garage Delivery service in more than 4,000 cities across the United States. Key In-Garage Delivery lets eligible Prime members enjoy contactless package delivery securely inside their garage, and offers convenient delivery confirmation for customers using the Key by Amazon app.

This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20201112005630/en/

Originally launched in 50 cities, the Key In-Garage Delivery service is expanding to Prime members in over 4,000 cities and towns across the U.S. including: New York, Los Angeles, Chicago, Philadelphia, Dallas, Washington D.C., Houston, Boston, Atlanta and Phoenix; and thousands of surrounding areas. (Photo: Business Wire)

Originally launched in 50 cities, the Key In-Garage Delivery service is expanding to Prime members in over 4,000 cities and towns across the U.S. including: New York, Los Angeles, Chicago, Philadelphia, Dallas, Washington D.C., Houston, Boston, Atlanta and Phoenix; and thousands of surrounding areas. (Photo: Business Wire)

“Customers tell us they appreciate the convenience and peace of mind that in-garage delivery offers, and we’re happy to expand the service to thousands of additional cities,” said Pete Gerstberger, Head of Key by Amazon. “With this latest expansion, Amazon customers in thousands of big cities and small towns across the U.S. can now enjoy another Prime benefit with convenient, contactless deliveries right in their garage, all backed by the Key by Amazon Happiness Guarantee.”

Key In-Garage Delivery lets eligible Prime members with a myQ smart garage door opener receive packages securely inside their garage. Once they link their myQ app with Key, customers simply select “FREE In-Garage Delivery” at checkout on Amazon.com. Packages are securely delivered by a delivery service professional, and customers can easily use the Key by Amazon app or the Amazon mobile shopping app to be notified when their package is delivered. To view videos of their delivery, customers can also use a compatible Ring smart home camera with their Ring Protect Plan, or LiftMaster Smart Garage Camera powered by myQ with a myQ Video Storage Subscription.

Originally launched in 50 cities, the Key In-Garage Delivery service is expanding to Prime members in over 4,000 cities and towns across the U.S. including: New York, Los Angeles, Chicago, Philadelphia, Dallas, Washington D.C., Houston, Boston, Atlanta and Phoenix; and thousands of surrounding areas such as Astoria, NY; Valencia, CA; Oswego, IL; Elverson, PA; Farmersville, TX; Frederick, MD; Magnolia, TX; Salisbury, MA; Peachtree City, GA; and Casa Grande, AZ, among many others.

In addition to expanding in-garage delivery, Amazon is also launching Key In-Garage Grocery Delivery. Beginning today in five cities, this new service enables eligible Prime members to have their grocery orders from Whole Foods Market or Amazon Fresh delivered securely into their garage. The service will be available in select areas of Chicago, Dallas, Los Angeles, San Francisco, and Seattle before expanding to other cities in the U.S. For more information, customers can visit www.amazon.com/keygrocery to check their eligibility and enjoy a limited-time offer of a $20 Amazon credit after their first in-garage grocery order. 1

To learn more about delivery options for their zip code and how to sign up for Key In-Garage Delivery, customers can visit www.amazon.com/keypromo. For a limited time, new Key by Amazon customers can receive $30 in Amazon credits after their first in-garage delivery.2

About Amazon

Amazon is guided by four principles: customer obsession rather than competitor focus, passion for invention, commitment to operational excellence, and long-term thinking. Customer reviews, 1-Click shopping, personalized recommendations, Prime, Fulfillment by Amazon, AWS, Kindle Direct Publishing, Kindle, Fire tablets, Fire TV, Amazon Echo, and Alexa are some of the products and services pioneered by Amazon. For more information, visit amazon.com/about and follow @AmazonNews.

1 Terms and conditions apply. Find them at www.amazon.com/keygrocery to learn more.

2 Terms and conditions apply. Find them at amazon.com/keypromo to learn more.

Amazon.com, Inc.

Media Hotline

[email protected]

www.amazon.com/pr

KEYWORDS: United States North America Washington

INDUSTRY KEYWORDS: Men Mobile/Wireless Online Retail Internet Hardware Supermarket Consumer Electronics Consumer Technology Food/Beverage Retail Women

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Originally launched in 50 cities, the Key In-Garage Delivery service is expanding to Prime members in over 4,000 cities and towns across the U.S. including: New York, Los Angeles, Chicago, Philadelphia, Dallas, Washington D.C., Houston, Boston, Atlanta and Phoenix; and thousands of surrounding areas. (Photo: Business Wire)

AJR Ready to Make a ‘BANG!’ on UScellular’s Instagram

AJR Ready to Make a ‘BANG!’ on UScellular’s Instagram

Pop Trio to Take Part in National Sweepstakes, Free Acoustic Virtual Performance as Part of Wireless Carrier’s Campaign for Customers and Fans

CHICAGO–(BUSINESS WIRE)–
UScellular™ announced it is teaming with pop trio AJR to encourage others to use their voice and technology to drive positive change in the world. While attending concerts in-person haven’t been possible these last few months, through the power of wireless tech, UScellular and AJR will look to bring the positivity to fans instead.

This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20201112005646/en/

AJR to Take Part in National Sweepstakes, Free Acoustic Virtual Performance as Part of UScellular Campaign for Customers and Fans (Photo courtesy of AJR)

AJR to Take Part in National Sweepstakes, Free Acoustic Virtual Performance as Part of UScellular Campaign for Customers and Fans (Photo courtesy of AJR)

UScellular is creating several opportunities for customers and fans across the country to connect with AJR. Fans will have a chance to score an exclusive virtual meet-and-greet with the “Burn the House Down” and “BANG!” artists. Registration for the giveaway ends on December 13. The band will also perform an acoustic virtual concert on December 18 at 8 p.m. CT., where AJR will perform a free 30-minute acoustic set available to anyone who registers.

“One of the most fulfilling aspects about working with musical talents like AJR, is sharing their interests and passions outside of music,” said Shelly Pluta, senior director of brand marketing for UScellular. “These brothers create positive energy, supporting those in need and righting wrongs that impact local communities. UScellular has a similar focus to connect customers in its communities to who and what is most important in their lives. We hope that through this campaign, we’re able to bring enjoyment and a sense of connection to those that have needed it this past year.”

To help celebrate the campaign launch, UScellular will host an “Ask Me Anything” Instagram live session featuring AJR on Monday, November 16, where fans will have a chance to ask questions and interact with the band at 8 p.m. CT.

“From the very beginning, we’ve wanted to maintain relationships with our fans that have helped us build a community over the last 8-10 years since we started playing live shows,” said Adam Met of AJR. “We feel like UScellular does the same thing — really supporting their community as much as possible, so there’s a lot of overlap.”

To register for the concert, enter the meet-and-greet sweepstakes and to find out more details, go to UScellularconnects.com.

NO PURCHASE NECESSARY. Open to residents of the 50 United States/D.C. 18 yrs+ (19+ in AL & NE). Void where prohibited. Ends 12/13/20. See Official Rules at uscellularconnects.com/rules/ for full details.

About AJR

AJR is a genre bending multi-Platinum band from New York City. The band’s music has crossed more than two billion streams worldwide and 200 million YouTube views. They’ve earned numerous accolades including “Sober Up” as Spotify’s ‘Best Rock Songs of 2010’s’ and “Weak” included in Apple Music‘s ‘Best Alternative Songs of 2010’s’ list. They’ve appeared at festivals including Forecastle, Lollapalooza, Reading and Leeds, Bumbershoot, sold more than 150,000 tickets in 2019, and performed on Jimmy Kimmel Live!, Good Morning America and Today.

About UScellular

UScellular is the fourth-largest full-service wireless carrier in the United States, providing national network coverage and industry-leading innovations designed to elevate the customer experience. The Chicago-based carrier is building a stronger network with the latest 5G technology and offers a wide range of communication services that enhance consumers’ lives, increase the competitiveness of local businesses and improve the efficiency of government operations. It is ranked #1 in the North Central Region in the J.D. Power 2020 Wireless Network Quality Performance Study – Volume 2. To learn more about UScellular, visit one of its retail stores or www.uscellular.com. To get the latest news, promos and videos, connect with UScellular on Facebook.com/uscellular, Twitter.com/uscellular and YouTube.com/uscellularcorp.

Anthony Garcia

UScellular Media Relations

Office: 773-399-4871

[email protected]

KEYWORDS: United States North America Illinois

INDUSTRY KEYWORDS: Telecommunications Social Media Music Communications Technology Events/Concerts Mobile/Wireless Entertainment

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AJR to Take Part in National Sweepstakes, Free Acoustic Virtual Performance as Part of UScellular Campaign for Customers and Fans (Photo courtesy of AJR)

Akers Biosciences and MyMD Pharmaceuticals Sign Definitive Merger Agreement

Akers Biosciences and MyMD Pharmaceuticals Sign Definitive Merger Agreement

Immunotherapies focused on age-related disorders and autoimmune diseases entering Phase 2 clinical trials

Lead molecule MYMD-1 inhibits production of tumor necrosis factor alpha (TNF-α), a cell signaling protein involved in systemic inflammation, in preclinical studies

Entered into Securities Purchase Agreement for $18M private placement of common stock and warrants priced at-the-market under Nasdaq Rules

BALTIMORE & THOROFARE, N.J.–(BUSINESS WIRE)–MyMD Pharmaceuticals, Inc. (“MyMD”) and Akers Biosciences, Inc. (“Akers”) (NASDAQ: AKER) today jointly announced that they have entered into a definitive merger agreement. Upon closing the transaction, the combined company is expected to be renamed MyMD Pharmaceuticals, Inc. and remain listed on the Nasdaq under the new ticker symbol “MYMD.”

The companies plan to hold a video conference for investors on Wednesday, November 18, 2020 at 4:15 p.m. ET to provide additional context on the integrated company, the clinical pipeline and drug development plan, and the commercial potential of the targeted indications. To participate in the briefing session, please click on the link below to register.

Following the merger, the two companies will join as one to focus on developing and commercializing MyMD’s novel immunotherapy pipeline assets, including MYMD-1, a first-in-class drug being developed to treat autoimmune and age-related diseases, including extending the human lifespan. MYMD-1 has been shown to be effective in regulating the immune system from causing age-related diseases in preclinical studies and MyMD believes that it is the first oral small molecule regulator of tumor necrosis factor alpha (TNF-α) capable of crossing the blood-brain barrier. Looking forward, MyMD intends to also continue to develop its second asset, SUPERA-1R, a drug platform based on a patent-protected, synthetic derivative of cannabidiol (CBD) that seeks to target key cannabinoid receptors.

A Phase 1 study on MYMD-1 has been completed, with plans to begin two Phase 2 clinical trials in Q1 2021 and additional Phase 2 clinical trials throughout 2021. Preclinical data, showing the effectiveness of MyMD-1 in treating autoimmune diseases, were compiled by nationally recognized researchers and laid the foundation for the studies, securing peer-reviewed publications in The Journal of Immunology and the Journal of Neuroimmunology.

“Over the last seven years, MyMD has advanced its robust drug development program, achieving very encouraging preclinical and Phase 1 clinical data,” said Chris Chapman, M.D., Chief Medical Officer of MyMD. “As we enter Phase 2 clinical trials and continue to advance our drug candidates toward commercialization–we believe this merger is the natural next step for us. Gaining access to the public capital markets, along with Akers’ capital resources, should allow us to accelerate our plans and elevate MyMD within the emerging fields of aging, immunometabolic regulation and TNFα inhibition.”

The mechanism of action for MYMD-1 involves shutting down the production of TNF-α, offering the potential to reshape clinical guidelines and treatment approaches for aging and a number of autoimmune diseases including diabetes, rheumatoid arthritis and multiple sclerosis.

Reflecting on the rationale for the merger, Chris Schreiber, Executive Chairman and President of Akers, stated, “We are excited about this strategic opportunity to focus on MyMD’s promising clinical development program and worldwide patent position. Through this transaction, the company will be committed to delivering novel, multi-indication platform drugs designed to extend healthy lifespan and treat the source of chronic autoimmune diseases. We are highly excited about MyMD’s broad development program focused on two drug platforms that address enormous market potential. We believe that our merger with MyMD should provide us with additional value creation opportunities, in addition to our COVID-19 vaccine candidate that we have been working with our partners in India to develop.”

Management and Organization

The combined company will be led by Chris Chapman, M.D., who will become President and Chief Medical Officer of MyMD, and Adam Kaplin, M.D., who will become Chief Scientific Officer of MyMD, and is planned to be headquartered in Baltimore, Maryland. Dr. Chapman is the founder and CEO of Chapman Pharmaceutical Consulting Inc. and will bring extensive experience working with biotechnology companies in the design of clinical trial protocols, conducting clinical trials and advising on regulatory and medical affairs. Dr. Kaplin, the prior founder and chief of the Neuropsychiatric CNS Autoimmune Consultation Clinic, at the Johns Hopkins Multiple Sclerosis Center of Excellence, and an assistant professor of psychiatry and behavioral sciences at the Johns Hopkins University School of Medicine, has consulted with multiple hospitals, biotechnology companies and non-profit organizations on medical and development matters.

Transaction Details

On a pro forma basis and based upon the number of shares of Akers common stock to be issued in the merger, current Akers’ shareholders will own approximately 20% of the combined company, on a fully diluted basis, and current MyMD’s shareholders will own approximately 80% of the combined company on a fully diluted basis (excluding the effect of warrants issued in the below described private placement). The merger agreement also provides for additional contingent payments in cash and shares to the stockholders of MyMD under certain circumstances. The merger is expected to close in the first half of 2021, subject to the approval of Akers’ shareholders at a special shareholder meeting, as well as other customary closing conditions.

In connection with the definitive merger agreement, Akers agreed to loan MyMD up to $3 million pursuant to a secured promissory note. The note bears interest at 5% per annum, has a maturity date of April 15, 2022 and is secured by a first lien on MyMD’s assets.

Private Placement

Concurrently with the execution of the merger agreement with MyMD, Akers entered into a securities purchase agreement with certain accredited investors to raise $18 million through the issuance of up to 9,765,933 shares of common stock (or common stock equivalents) and accompanying warrants to purchase an aggregate of up to 9,765,933 shares of common stock at $1.85 per share of common stock and accompanying warrant. The warrants are immediately exercisable at an exercise price of $2.06 per share, with an expiration date of five and one-half years after the date of issuance. The offer and sale of the foregoing securities are being made in a transaction not involving a public offering and have not been registered under the Securities Act of 1933, as amended (the “Securities Act”), or applicable state securities laws.

Accordingly, the securities may not be reoffered or resold in the United States except pursuant to an effective registration statement or an applicable exemption from the registration requirements of the Securities Act and such applicable state securities laws.

Under an agreement with the investors, the Company is required to file a registration statement with the Securities and Exchange Commission covering the resale of the shares of common stock to be issued to the investors and to use best efforts to have the registration statement declared effective as promptly as practical thereafter.

The closing of the private placement is subject to the satisfaction of certain customary closing conditions set forth in the securities purchase agreement.

About Akers Biosciences Inc.

Akers Biosciences is pursuing rapid development and manufacturing of a COVID-19 vaccine candidate in collaboration with Premas Biotech PVT Ltd.

About MyMD Pharmaceuticals, Inc:

MyMD is a clinical stage pharmaceutical company committed to extending healthy lifespan by focusing on developing two therapeutic platforms. MYMD-1 is a drug platform based on a clinical stage small molecule that regulates the immunometabolic system to control TNF-α and other pro-inflammatory cytokines. MYMD-1 is being developed to treat autoimmune diseases, including those currently treated with TNF-α blocking drugs, and aging and longevity. SUPERA-1R is a drug platform based on a novel (patent pending) synthetic derivative of cannabidiol (CBD) that targets numerous key receptors including CB2 and opioid receptors and inhibits monoamine oxidase. SUPERA-1R is being developed to address the rapidly growing CBD market, that includes FDA approved drugs and CBD products not currently regulated as a drug. For more information, visit www.mymd.com.

No Offer or Solicitation

This communication shall not constitute an offer to sell or the solicitation of an offer to sell or the solicitation of an offer to buy any securities, nor shall there be any sale of securities in any jurisdiction in which such offer, solicitation or sale would be unlawful prior to registration or qualification under the securities laws of any such jurisdiction. No public offer of securities shall be made except by means of a prospectus meeting the requirements of Section 10 of the Securities Act of 1933, as amended.

Important Additional Information Will be Filed with the SEC

In connection with the proposed transaction between Akers and MyMD, Akers intends to file relevant materials with the SEC, including a registration statement that will contain a proxy statement and prospectus. AKERS URGES INVESTORS AND STOCKHOLDERS TO READ THESE MATERIALS CAREFULLY AND IN THEIR ENTIRETY WHEN THEY BECOME AVAILABLE BECAUSE THEY WILL CONTAIN IMPORTANT INFORMATION ABOUT AKERS, THE PROPOSED TRANSACTION AND RELATED MATTERS. Investors and shareholders will be able to obtain free copies of the proxy statement, prospectus and other documents filed by Akers with the SEC (when they become available) through the website maintained by the SEC at www.sec.gov. In addition, investors and shareholders will be able to obtain free copies of the proxy statement, prospectus and other documents filed by Akers with the SEC by contacting Investor Relations by mail at Akers Biosciences, Inc., Attn: Investor Relations, 201 Grove Road, West Deptford, NJ 08086. Investors and stockholders are urged to read the proxy statement, prospectus and the other relevant materials when they become available before making any voting or investment decision with respect to the proposed transaction.

Participants in the Solicitation

Akers and MyMD, and each of their respective directors and executive officers and certain of their other members of management and employees, may be deemed to be participants in the solicitation of proxies in connection with the proposed transaction. Information about Akers’ directors and executive officers is included in Akers’ Annual Report on Form 10-K for the year ended December 31, 2019, filed with the SEC on March 25, 2020, as amended on October 21, 2020, and the proxy statement for Akers’ 2020 annual meeting of stockholders, filed with the SEC on July 29, 2020. Additional information regarding these persons and their interests in the transaction will be included in the proxy statement relating to the transaction when it is filed with the SEC. These documents can be obtained free of charge from the sources indicated above.

Cautionary Statement Regarding Forward-Looking Statements

Certain statements contained in this communication regarding matters that are not historical facts are forward-looking statements within the meaning of Section 21E of the Securities and Exchange Act of 1934, as amended, and the Private Securities Litigation Reform Act of 1995, known as the PSLRA. These include statements regarding management’s intentions, plans, beliefs, expectations or forecasts for the future, and, therefore, you are cautioned not to place undue reliance on them. No forward-looking statement can be guaranteed, and actual results may differ materially from those projected. Akers and MyMD undertake no obligation to publicly update any forward-looking statement, whether as a result of new information, future events or otherwise, except to the extent required by law. We use words such as “anticipates,” “believes,” “plans,” “expects,” “projects,” “future,” “intends,” “may,” “will,” “should,” “could,” “estimates,” “predicts,” “potential,” “continue,” “guidance,” and similar expressions to identify these forward-looking statements that are intended to be covered by the safe-harbor provisions of the PSLRA. Such forward-looking statements are based on our expectations and involve risks and uncertainties; consequently, actual results may differ materially from those expressed or implied in the statements due to a number of factors, including, but not limited to, risks relating to the completion of the merger, including the need for stockholder approval and the satisfaction of closing conditions; Aker’s inability to consummate the private placement; the cash balances of the combined company following the closing of the merger; the ability of Akers to remain listed on the Nasdaq Capital Market in connection with the merger; and expected merger-related cash outlays, including the timing and amount of those outlays. Risks and uncertainties related to MyMD that may cause actual results to differ materially from those expressed or implied in any forward-looking statement include, but are not limited to: the timing of, and MyMD’s ability to, obtain and maintain regulatory approvals for clinical trials of MyMD’s pharmaceutical candidates, the timing and results of MyMD’s planned clinical trials for its pharmaceutical candidates, the amount of funds MyMD requires for its pharmaceutical candidates; increased levels of competition; changes in political, economic or regulatory conditions generally and in the markets in which MyMD operates; MyMD’s ability to retain and attract senior management and other key employees; MyMD’s ability to quickly and effectively respond to new technological developments; MyMD’s ability to protect its trade secrets or other proprietary rights, operate without infringing upon the proprietary rights of others and prevent others from infringing on MyMD’s proprietary rights; and the impact of the ongoing COVID-19 pandemic on MyMD’s results of operations, business plan and the global economy.

New factors emerge from time to time and it is not possible for us to predict all such factors, nor can we assess the impact of each such factor on the business or the extent to which any factor, or combination of factors, may cause actual results to differ materially from those contained in any forward-looking statements. These risks, as well as other risks associated with the combination, will be more fully discussed in the proxy statement/prospectus that will be included in the registration statement that will be filed with the SEC in connection with the proposed transaction. Additional risks and uncertainties are identified and discussed in the “Risk Factors” section of Akers’ Annual Report on Form 10-K, Quarterly Reports on Form 10-Q and other documents filed from time to time with the SEC. Forward-looking statements included in this release are based on information available to Akers and MyMD as of the date of this release. Neither Akers nor MyMD undertakes any obligation to update such forward- looking statements to reflect events or circumstances after the date of this release.

Investor Contact:

Brett Mass

646-536-7331

[email protected]

www.haydenir.com

Media Contact:

Will Johnson

201-465-8019

[email protected]

www.antennagroup.com

KEYWORDS: Maryland New Jersey United States North America

INDUSTRY KEYWORDS: Clinical Trials Biotechnology Managed Care Health Pharmaceutical General Health Other Science Science Oncology

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AIG Announces Executive Promotions

AIG Announces Executive Promotions

NEW YORK–(BUSINESS WIRE)–
American International Group, Inc. (NYSE: AIG) today announced that Lucy Fato, Executive Vice President & General Counsel, has taken on additional responsibilities in the newly created position Global Head of Communications and Government Affairs.

This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20201112005627/en/

Lucy Fato (Photo: Business Wire)

Lucy Fato (Photo: Business Wire)

In her expanded role, Ms. Fato has assumed responsibility for Global Communications in addition to the Government Relations and Public Policy group, which she has overseen since May. Ms. Fato will continue to report to Brian Duperreault, Chief Executive Officer of AIG, and, with respect to Global Communications, will report to Peter S. Zaffino, President and CEO-elect of AIG.

Mr. Zaffino stated, “Achieving excellence in all that we do requires exceptional talent and I am delighted to recognize Lucy’s important contributions to AIG with this well-deserved promotion. Lucy has a deep understanding of the complex environment we operate in and already plays a central role in communicating with AIG’s stakeholders. I look forward to continuing to partner with Lucy and know she will bring the same level of rigor and discipline to this new role as she has throughout her legal career.”

The Company also announced that Emily Garbaccio has been promoted to Global Head of Corporate Communications, AIG, and Global Chief Marketing & Communications Officer, General Insurance, and has joined the General Insurance Executive Leadership Team. She will report to Lucy Fato and David McElroy, Chief Executive Officer, General Insurance and Executive Vice President, AIG.

Mr. McElroy said, “Since joining AIG in 2018, Emily has been a strategic and effective leader, making significant contributions to the Marketing & Communications function in General Insurance. She has deep experience developing communications strategies for a range of organizations going through significant periods of change and growth and we look forward to her continued leadership and perspective.”

Ms. Fato said, “As we strengthen AIG’s long-term strategic positioning, it is increasingly important that our stakeholders have a clear picture of our businesses, strategy and value proposition. I look forward to working with Emily and our global marketing and communications colleagues as we continue to work toward becoming a top performing company.”

Ms. Fato joined AIG in October 2017 as Executive Vice President & General Counsel. She was previously Managing Director, Head of the Americas and General Counsel at Nardello & Co., a global private investigative firm, where she remains on the Advisory Board. Prior to that, she was Executive Vice President & General Counsel of McGraw Hill Financial (now known as S&P Global) and Vice President, Deputy General Counsel and Corporate Secretary at Marsh & McLennan Companies. Ms. Fato began her legal career at the law firm Davis Polk & Wardwell, where she spent 14 years, including five as a partner in the capital markets group.

Ms. Garbaccio joined AIG in August 2018 as Global Head of Leadership and Transformation Communications, General Insurance and, in 2019, took on responsibility for communications related to AIG 200. Her background includes more than 20 years of in-house and agency leadership roles for both privately held and publicly traded companies, including Kate Spade, J.C. Penney, LaForce + Stevens and Burson-Marsteller.

American International Group, Inc. (AIG) is a leading global insurance organization. AIG member companies provide a wide range of property casualty insurance, life insurance, retirement solutions, and other financial services to customers in more than 80 countries and jurisdictions. These diverse offerings include products and services that help businesses and individuals protect their assets, manage risks and provide for retirement security. AIG common stock is listed on the New York Stock Exchange.

Additional information about AIG can be found at www.aig.com | YouTube: www.youtube.com/aig | Twitter: @AIGinsurance www.twitter.com/AIGinsurance | LinkedIn: www.linkedin.com/company/aig. These references with additional information about AIG have been provided as a convenience, and the information contained on such websites is not incorporated by reference into this press release.

AIG is the marketing name for the worldwide property-casualty, life and retirement, and general insurance operations of American International Group, Inc. For additional information, please visit our website at www.aig.com. All products and services are written or provided by subsidiaries or affiliates of American International Group, Inc. Products or services may not be available in all countries and jurisdictions, and coverage is subject to underwriting requirements and actual policy language. Non-insurance products and services may be provided by independent third parties. Certain property-casualty coverages may be provided by a surplus lines insurer. Surplus lines insurers do not generally participate in state guaranty funds, and insureds are therefore not protected by such funds.

Sabra Purtill (Investors): [email protected]

Shelley Singh (Investors): [email protected]

Jordan Robbins (Media): [email protected]

Claire Talcott (Media): [email protected]

KEYWORDS: United States North America New York

INDUSTRY KEYWORDS: Banking Professional Services Insurance Finance

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Lucy Fato (Photo: Business Wire)
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Emily Garbaccio (Photo: Business Wire)

TFF Pharmaceuticals to Present at the Jefferies Virtual London Healthcare Conference

TFF Pharmaceuticals to Present at the Jefferies Virtual London Healthcare Conference

Corporate presentation and live webcast scheduled for Thursday, November 19, 2020 at 2:55 PM ET

AUSTIN, Texas–(BUSINESS WIRE)–
TFF Pharmaceuticals, Inc. (NASDAQ: TFFP), a clinical-stage biopharmaceutical company focused on developing and commercializing innovative drug products based on its patented Thin Film Freezing (TFF) technology platform, has been invited to present at the Jefferies Virtual London Healthcare Conference, taking place virtually from November 17-19, 2020.

Glenn Mattes, President & CEO of TFF Pharmaceuticals, is scheduled to give a corporate overview on Thursday, November 19, 2020 at 2:55 PM ET, and will participate in one-on-one partnering meetings with investors and other conference attendees.

A live webcast of the presentation will be available at the following link: https://wsw.com/webcast/jeff141/tffp/1846800. Following the conference, an archived version of the webcast will be available under the Events Calendar tab in the Investors section of the Company’s website.

About TFF Pharmaceuticals’ Thin Film Freezing technology platform

TFF Pharmaceuticals’ Thin Film Freezing (TFF) platform was designed to improve the solubility and absorption of poorly water-soluble drugs and is particularly suited to generate dry powder particles with properties targeted for inhalation delivery, especially to the deep lung, an area of extreme interest in respiratory medicine. The TFF process results in a “Brittle Matrix Particle,” which possesses low bulk density, high surface area, and typically an amorphous morphology. allowing the particles to supersaturate when contacting the target site, such as lung tissue. Based upon laboratory experiments the aerodynamic properties of the particles are such that the portion of a drug deposited to the deep lung has the potential to reach as high as 75 percent.

About TFF Pharmaceuticals

TFF Pharmaceuticals, Inc. is a clinical-stage biopharmaceutical company focused on developing and commercializing innovative drug products based on its patented Thin Film Freezing, or TFF, technology platform. Early testing confirms that the TFF platform can significantly improve the solubility and absorption of poorly water-soluble drugs, a class of drugs that comprises approximately one-third of the major pharmaceuticals worldwide, thereby improving their pharmacokinetics. TFF Pharmaceuticals has two lead drug candidates: Voriconazole Inhalation Powder and Tac-Lac Inhalation Powder. The Company plans to add to this pipeline by collaborating with large pharmaceutical partners. The TFF Platform is protected by 42 patents issued or pending in the US and internationally. To learn more about TFF Pharmaceuticals and its product candidates, visit the Company’s website at https://tffpharma.com.

Company Contacts:

Glenn Mattes

President and CEO

TFF Pharmaceuticals, Inc.

[email protected]

737-802-1973

Kirk Coleman

Chief Financial Officer

TFF Pharmaceuticals, Inc.

[email protected]

817-989-6358

Investor Relations and Media Contact:

Paul Sagan

LaVoieHealthScience

[email protected]

617-953-4779

KEYWORDS: United States North America Texas

INDUSTRY KEYWORDS: Biotechnology Pharmaceutical Health

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AngioDynamics Announces Presentation of Positive Safety, Efficacy Results from RAPID Outcomes Database

AngioDynamics Announces Presentation of Positive Safety, Efficacy Results from RAPID Outcomes Database

Represents Largest Catheter Based Thromboaspiration Study Completed to Date

LATHAM, N.Y.–(BUSINESS WIRE)–
AngioDynamics, Inc. (NASDAQ: ANGO), a leading provider of innovative, minimally invasive medical devices for vascular access, peripheral vascular disease, and oncology, announced the safety and efficacy results from the Registry of AngioVac* System Procedures In Detail (RAPID) database. Results were shared by principal investigator John Moriarty, MD, FSIR, FSVM (Associate Professor of Radiology and Medicine, Cardiology—UCLA Interventional Radiology, David Geffen School of Medicine at UCLA), at the Vascular Interventional Advances (VIVA) 2020 meeting.

The registry was designed to evaluate the patterns of use, safety and efficacy of the AngioVac System in the bulk removal of undesirable intravascular material. The registry enrolled 234 patients across 21 sites, surpassing its 200-patient enrollment goal. Among enrolled patients, 48.3% had a mass in the right heart, 35.9% had caval thromboemboli, 8.5 % had catheter related thrombi, 1.7% had a pulmonary embolism** and 5.6% had a combination of the above.

“RAPID represents the largest catheter based thromboaspiration study completed to date, and we are pleased to share its positive findings,” said Scott Centea, AngioDynamics Sr. Vice President and General Manager, VIT/PAD. “A growing number of providers are recognizing the AngioVac System as a critically important tool in the treatment and removal of thrombi and emboli. The overwhelmingly positive results from the RAPID Registry demonstrate that the AngioVac System is appropriate for use by a wide range of providers treating thrombus, clot and vegetations in both peripheral deep vein thrombosis (DVT) and the right heart.”

Findings from the RAPID Registry have been accepted for publication in the Journal of Vascular and Interventional Radiology1.

The primary objective of the registry was to capture data on the use of the AngioVac System for various anatomic locations. Greater than 70% of clot/mass removal was achieved in a majority of the patient population. Overall, the study confirmed the AngioVac System to be versatile, safe and effective for the removal of vascular thrombi and cardiac masses across a broad range of patient populations.

“Our goal threshold was to remove over 70% of the clot, which we felt was clinically relevant, and each of the three main groups—the caval group, the right heart group, and the catheter associated clot group—were associated with very high rates of clot removal,” commented Dr. Moriarty. “In the first two years of the Registry, there were more caval thrombectomies than right heart mass procedures, and that flipped in the latter two years. If we were to extrapolate our trajectory, we would say that close to 70% of all procedures are being performed in the right heart. Additionally, the AngioVac System was successfully tested by a number of different practitioners, including cardiologists, EP cardiologists, cardiac surgeons, vascular surgeons, and interventional radiologists. Ultimately, the diversity of providers, combined with the efficacy and safety results, demonstrates the unique and versatile nature of the AngioVac System.”

Learn more about the AngioVac System at AngioVac.com.

About AngioDynamics, Inc.

AngioDynamics, Inc. is a leading provider of innovative, minimally invasive medical devices used by professional healthcare providers for vascular access, peripheral vascular disease, and oncology. AngioDynamics’ diverse product lines include market-leading ablation systems, vascular access products, angiographic products and accessories, drainage products, thrombolytic products and venous products. For more information, visit www.angiodynamics.com.

*AngioDynamics, the AngioDynamics logo, and AngioVac are trademarks and/or registered trademarks of AngioDynamics, Inc., an affiliate or subsidiary. All other trademarks are property of their respective owners.

**Indications for Use: The AngioVac Cannula is indicated for use as a venous drainage cannula and for removal of fresh, soft thrombi or emboli during extracorporeal bypass for up to 6 hours. The AngioVac Circuit is indicated for use in procedures requiring extracorporeal circulatory support for periods of up to six hours. For important AngioVac Cannula risk information, visit https://www.angiodynamics.com/about-us/risk-information/#bangiovaccann. For important AngioVac Circuit risk information, visit https://www.angiodynamics.com/about-us/risk-information/#cangiovac.

1. Moriarty et al, Endovascular removal of thrombus and right heart masses using the AngioVac system. Results of 234 patients from the prospective multicenter registry of AngioVac procedures in detail (RAPID). JVIR. Accepted for publication.

Investor Relations Contact:

AngioDynamics, Inc.

Stephen Trowbridge

518-795-1408

[email protected]

Media Contact:

AngioDynamics, Inc.

Saleem Cheeks

518-795-1174

[email protected]

KEYWORDS: United States North America New York

INDUSTRY KEYWORDS: Surgery Medical Devices Health Clinical Trials Oncology

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SailPoint to Participate at the RBC Capital Markets Global Technology, Internet, Media and Telecom Virtual Conference

SailPoint to Participate at the RBC Capital Markets Global Technology, Internet, Media and Telecom Virtual Conference

AUSTIN, Texas–(BUSINESS WIRE)–SailPoint Technologies Holdings, Inc. (NYSE: SAIL), the leader in identity management, today announced that Chief Financial Officer Jason Ream will participate in a fireside chat at the RBC Capital Markets Global Technology, Internet, Media and Telecom Virtual Conference on Wednesday, November 18, 2020 at 3:20 p.m. ET.

The presentations will be webcast live at https://investors.sailpoint.com. A replay of the presentations will be made available for a limited time.

About SailPoint

SailPoint, the leader in identity management, delivers an innovative approach to securing access across the enterprise with the SailPoint Predictive IdentityTM platform. With SailPoint, enterprises can ensure that everyone and everything has the exact access they need, exactly when they need it, intuitively and automatically. Powered by patented Artificial Intelligence (AI) and Machine Learning (ML) technologies, the SailPoint Predictive IdentityTM platform is designed to securely accelerate the business while delivering adaptive security, continuous compliance, and improved business efficiency. As an identity pioneer and market leader serving some of the world’s most prominent global companies, SailPoint consistently pushes the industry to rethink identity to the benefit of their customers’ dynamic business needs.

Stay up-to-date on SailPoint by following us on Twitter and LinkedIn and by subscribing to the SailPoint blog.

Investor Relations

ICR for SailPoint

Brian Denyeau, 512-664-8916

[email protected]

Media Relations

SailPoint Technologies Holdings, Inc.

Jessica Sutera, 978-278-5411

[email protected]

KEYWORDS: Texas United States North America

INDUSTRY KEYWORDS: Telecommunications Software Networks Internet Data Management Technology Mobile/Wireless Other Technology

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CyberArk to Webcast Needham Virtual Security, Networking, and Communications Conference

CyberArk to Webcast Needham Virtual Security, Networking, and Communications Conference

NEWTON, Mass. & PETACH TIKVA, Israel–(BUSINESS WIRE)–CyberArk (NASDAQ: CYBR), the global leader in privileged access management, today announced that it will webcast its presentation at the upcoming virtual conference:

Needham Virtual Security, Networking, and Communications Conference

Tuesday, November 17, 2020

9:30 a.m. ET

The presentation will be webcast, and an archive of the presentation will be available for a limited time under the “Events & Presentations” section on the company’s investor relations website (http://investors.cyberark.com/).

About CyberArk

CyberArk(NASDAQ: CYBR) is the global leader in privileged access management, a critical layer of IT security to protect data, infrastructure and assets across cloud and hybrid environments, and throughout the DevOps pipeline. CyberArk delivers the industry’s most complete solution to reduce risk created by privileged credentials and secrets. The company is trusted by the world’s leading organizations, including more than 50 percent of the Fortune 500, to protect against external attackers and malicious insiders. A global company, CyberArk is headquartered in Petach Tikva, Israel, with U.S. headquarters located in Newton, Mass. The company also has offices throughout the Americas, EMEA, Asia Pacific and Japan. To learn more about CyberArk, visit www.cyberark.com, read the CyberArk blogs or follow on Twitter via @CyberArk, LinkedIn or Facebook.

Copyright © 2020 CyberArk Software. All Rights Reserved.All other brand names, product names, or trademarks belong to their respective holders.

Investor Relations Contact:

Erica Smith

CyberArk

617-558-2132

[email protected]

Media Contact:

Liz Campbell

CyberArk

617-558-2191

[email protected]

KEYWORDS: United States North America Israel Middle East Massachusetts

INDUSTRY KEYWORDS: Technology Networks Internet Security

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