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Osivax pairs Phase II flu vaccine with GC Biopharma's marketed shot in combination deal

Osivax pairs Phase II flu vaccine with GC Biopharma's marketed shot in combination deal

France-based Osivax and South Korea-based GC Biopharma (KRX: 006280) have announced a long-term collaboration to develop a single-injection combination influenza vaccine, pairing Osivax's Phase II nucleoprotein-targeting candidate OVX836 with GC Biopharma's WHO-prequalified inactivated seasonal vaccine GC FLU.

Under the agreement, GC Biopharma grants Osivax a non-exclusive, sublicensable global license to use GC FLU in combination with OVX836, excluding Korea and Japan. Osivax will lead global development and commercialization outside Korea; GC Biopharma retains exclusive Korean rights, receives royalties, and commits to long-term GC FLU supply. Financial terms were not disclosed.

Unlike a conventional biotech out-license, the agreement gives Osivax rights to incorporate GC Biopharma's marketed vaccine into a combination product that Osivax will develop and commercialize outside Korea.

OVX836 is described by Osivax as targeting the nucleoprotein (NP), a conserved internal influenza A antigen, via the company's oligoDOM self-assembling nanoparticle platform, with the aim of eliciting broad T-cell responses across influenza A strains. GC FLU targets the variable hemagglutinin surface antigen, generating antibody responses. The companies assert the combination is designed to produce complementary immune coverage. Osivax published Phase IIa co-administration data in Vaccines in July 2025, reporting that OVX836 was well tolerated alongside a standard-dose inactivated influenza vaccine and induced complementary immune responses — the direct scientific basis for the GC FLU combination approach.

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OVX836 has now been tested in seven clinical trials with more than 4,000 participants. Osivax dosed the first participant in its Phase IIb trial in September 2025, meaning the GC Biopharma deal was structured during active Phase IIb enrollment, before efficacy readout. Osivax also completed last patient last visit in a Phase IIa booster trial in June 2025 and secured a USD 19.5 million award from the US Biomedical Advanced Research and Development Authority (BARDA) in August 2025 to advance OVX836 for pandemic and seasonal preparedness.

The GC Biopharma deal represents Osivax's first commercial licensing arrangement for OVX836. The sublicensable nature of the license gives Osivax flexibility to bring in future commercial partners without renegotiating with GC Biopharma.


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