Osivax announced that it has entered a research collaboration with the National Institute of Allergy and Infectious Diseases, part of the National Institutes of Health, to conduct a preclinical evaluation combining Osivax’ T-cell based influenza candidate, OVX836, with a range of the NIAID Vaccine Research Center ’s influenza vaccine candidates.
“This research collaboration is an extension of our ongoing interactions with NIAID and represents a critical step forward in addressing the urgent need for an improved influenza vaccine to protect against influenza strains with pandemic potential,” commented Alexandre Le Vert, CEO and Co-Founder of Osivax. “In combining OVX836 with the NIAID candidates, we intend to unlock the synergy of pairing T- and B-cell activation to drastically improve influenza protection against future pandemic outbreaks. The data we will gather from this collaboration will be invaluable to this effort.”
Osivax’ OVX836 is a nucleoprotein-targeting influenza vaccine developed using the company’s proprietary oligoDOM® technology. Recently published clinical data from the company’s Phase 2a trial revealed that OVX836 induced a significant increase of NP-specific cellular immune responses, including CD4+ and CD8+ T-cells, and initial efficacy signals while being safe and well-tolerated. Osivax is pursuing the combination with the NIAID’s next-generation vaccine candidates as a strategy to significantly improve the efficacy and cross-protection against existing and future pandemic influenza strains.
Under the terms of the collaboration, NIAID will provide its novel, self-assembling ferritin nanoparticles that serve as scaffolding to display multiple copies of HA protein, a protein expressed on the surface of influenza viruses, to Osivax for in vivo preclinical studies in combination with OVX836. Preclinical data from the NIAID vaccine candidates indicate an enhanced breadth of the immune response in animal models compared to traditional seasonal vaccines, thus also offering potential protection against influenza strains not included in the vaccine. NIAID is currently conducting Phase 1 clinical trials to assess safety and immunogenicity in humans (NCT03814720 and NCT04579250).
About OVX836
Osivax’ influenza vaccine, OVX836 targets the nucleoprotein (NP), a highly conserved internal antigen. Unlike surface antigens, NP is much less likely to mutate, providing a broader and more universal immune response. Osivax’ oligoDOM® technology enables the design and production of recombinant version of the NP which self-assembles into a nanoparticle, thus triggering powerful T-and B-cell immune responses. OVX836 has shown promising safety, immunogenicity, and efficacy in preclinical and clinical trials (Phase 1 and Phase 2a).
About Osivax
Osivax is a biopharmaceutical company leveraging its novel, self-assembling nanoparticle platform technology, oligoDOM®, to transform current and new vaccines by generating superior T-cell responses in addition to strong and sustained B cell responses against highly mutating viruses. The company is establishing proof of concept with its highly validated lead influenza candidate, OVX836, which is currently in Phase 2 testing with over 500 subjects tested. Osivax is also exploring the broader application of its technology in both mRNA and subunit vaccines against a variety of indications. The company will expand into other infectious disease indications through combinations and collaborations worldwide.
About NIAID
NIAID conducts and supports basic and applied research to better understand, treat, and ultimately prevent infectious, immunologic, and allergic diseases. For more than 60 years, NIAID research has led to new therapies, vaccines, diagnostic tests, and other technologies that have improved the health of millions of people in the United States and around the world. News releases, fact sheets and other NIAID-related materials are available on the NIAID website.
For further information: www.osivax.com
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Alexandre LE VERT, CEO
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Valeria Fisher or Desmond James
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Source: Osivax
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