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Bristol Myers Squibb and The Rockefeller University Announce License Agreement for SARS-CoV-2 Neutralizing Monoclonal Antibody Combination for the Treatment of COVID-19

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Bristol Myers Squibb (NYSE: BMY) has secured a global exclusive license from The Rockefeller University to develop and commercialize a new monoclonal antibody (mAb) treatment targeting the SARS-CoV-2 virus. This novel therapy combines two highly potent mAbs designed to neutralize the virus and block its spike protein, making it effective against various variants. Phase 1 clinical trials are currently underway to determine dosing and safety. Should the trials succeed, Bristol Myers Squibb aims to ensure the treatment's global accessibility and affordability.

Positive
  • Exclusive license from Rockefeller University for mAb COVID-19 treatment.
  • Potential for effective treatment against multiple SARS-CoV-2 variants.
  • Phase 1 clinical trials initiated, moving towards registrational program.
Negative
  • Regulatory approval for the mAb treatment remains uncertain.
  • Potential delays in realizing expected benefits from the agreement.

Bristol Myers Squibb (NYSE: BMY) and The Rockefeller University today announced that they have entered into a definitive agreement under which Bristol Myers Squibb has been granted a global exclusive license to develop, manufacture and commercialize Rockefeller’s novel monoclonal antibody (“mAb”) duo treatment that neutralizes the SARS-CoV-2 virus for therapy or prevention of COVID-19.

Despite the increasing availability of the vaccines, there will continue to be patients who contract COVID-19 and will need treatment for their infection. This novel treatment is a combination of two mAbs directed at blocking the SARS-CoV-2 spike protein and neutralizing the virus. The mAbs have been engineered to be highly potent and stable, allowing them to last longer in the bloodstream. Preclinical data suggest that this could enable effective treatment against multiple variants of the virus using a low dose subcutaneous administration, which would increase access to the medicine by eliminating the need for intravenous infusion.

Ultimately, should the clinical development be successful, these advantages could potentially help expand access globally, including to low- and middle-income countries and to communities where healthcare resources are limited—a goal that both institutions will jointly work towards.

Phase 1 clinical trials to assess dosing for IV and subcutaneous formulations, and to assess safety for the mAb duo, were initiated by Rockefeller in mid-January. Planning is underway with the goal of moving rapidly to a registrational program following readout of the phase 1 study taking place at Rockefeller University Hospital.

“We look forward to continuing to work with The Rockefeller University in this crucial effort,” said Ho Sung Cho, Ph.D., Senior Vice President, Discovery Biotherapeutics, Bristol Myers Squibb. “Bristol Myers Squibb has supported the development and manufacturing of clinical supplies for Rockefeller to begin the Phase 1 trial and we are committed to leveraging our capabilities and resources in an effort to expeditiously develop and bring this potential treatment to patients and further address the challenges of the pandemic.”

“The two highly potent antibodies against SARS-CoV-2, discovered by Rockefeller scientists, have the potential to play an important role in treating COVID-19 patients,” said Richard P. Lifton, President, The Rockefeller University. “New treatment options are urgently needed that treat mild to moderate disease and prevent development of severe disease in high-risk patients. Our collaboration with BMS will help us accelerate development timelines and support rapid delivery to patients.”

Included in the terms of the agreement, Rockefeller is entitled to receive royalty payments on future sales. Should the clinical development be successful, Bristol Myers Squibb will work to enable availability and affordability of this potential treatment to patients globally.

About SARS-CoV-2 mAb Combo

Rockefeller has discovered two complementary antibodies to the SARS-CoV-2 spike protein that synergistically neutralize the virus in vitro and in animal models. The two antibodies have shown activity against several known SARS-CoV-2 mutants and it is believed that their co-administration could reduce the possibility of mutant virus escape. The two antibodies are potentially unique as pertains to their long half-life in humans and high affinity for the spike protein. The longer half-life has been enabled by leveraging Xencor’s Fc engineering technology.

About Bristol Myers Squibb

Bristol Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases. For more information about Bristol Myers Squibb, visit us at BMS.com or follow us on LinkedIn, Twitter, YouTube, Facebook and Instagram.

Celgene and Juno Therapeutics are wholly owned subsidiaries of Bristol-Myers Squibb Company. In certain countries outside the U.S., due to local laws, Celgene and Juno Therapeutics are referred to as, Celgene, a Bristol Myers Squibb company and Juno Therapeutics, a Bristol Myers Squibb company.

About The Rockefeller University

The Rockefeller University is the world’s leading biomedical research university and is dedicated to conducting innovative, high-impact research to improve the understanding of life for the benefit of humanity. The university’s unique approach to science, with only 70 faculty, each selected for pursuit of highly innovative ideas, has led to many of the world’s most revolutionary and transformative contributions to biology and medicine. During Rockefeller’s 120-year history, Rockefeller scientists have won 26 Nobel Prizes, 24 Albert Lasker Medical Research Awards, and 20 National Medals of Science.

Cautionary Statement Regarding Forward-Looking Statements

This press release contains “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995 regarding, among other things, the research, development and commercialization of pharmaceutical products and the agreement with The Rockefeller University. All statements that are not statements of historical facts are, or may be deemed to be, forward-looking statements. Such forward-looking statements are based on historical performance and current expectations and projections about our future financial results, goals, plans and objectives and involve inherent risks, assumptions and uncertainties, including internal or external factors that could delay, divert or change any of them in the next several years, that are difficult to predict, may be beyond our control and could cause our future financial results, goals, plans and objectives to differ materially from those expressed in, or implied by, the statements. These risks, assumptions, uncertainties and other factors include, among others, that the expected benefits of, and opportunities related to, the agreement with The Rockefeller University may not be realized by Bristol Myers Squibb or may take longer to realize than anticipated and that Rockefeller’s novel monoclonal antibody duo treatment may not receive regulatory approval for the treatment of COVID-19. No forward-looking statement can be guaranteed. Forward-looking statements in this press release should be evaluated together with the many risks and uncertainties that affect Bristol Myers Squibb’s business and market, particularly those identified in the cautionary statement and risk factors discussion in Bristol Myers Squibb’s Annual Report on Form 10-K for the year ended December 31, 2019, as updated by our subsequent Quarterly Reports on Form 10-Q, Current Reports on Form 8-K and other filings with the Securities and Exchange Commission. The forward-looking statements included in this document are made only as of the date of this document and except as otherwise required by applicable law, Bristol Myers Squibb undertakes no obligation to publicly update or revise any forward-looking statement, whether as a result of new information, future events, changed circumstances or otherwise.

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FAQ

What treatment has Bristol Myers Squibb licensed from Rockefeller University?

Bristol Myers Squibb has licensed a novel monoclonal antibody duo treatment for COVID-19.

What is the significance of the mAb duo developed by Rockefeller University?

The mAb duo is designed to neutralize SARS-CoV-2 and may work against multiple virus variants.

What are the next steps for the COVID-19 mAb treatment by Bristol Myers Squibb?

Phase 1 trials are underway to assess dosing and safety, with plans for a registrational program.

How will Bristol Myers Squibb ensure global access to the mAb treatment?

The company aims to make the potential treatment accessible and affordable globally, especially in low- and middle-income countries.

When did Bristol Myers Squibb initiate clinical trials for the mAb treatment?

Phase 1 clinical trials were initiated by Rockefeller University in mid-January.

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