Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
LC16m8 is a next-generation, attenuated smallpox vaccine derived from the Lister vaccinia virus strain and produced in cell culture. It is designed to have an improved safety profile compared to traditional smallpox vaccines while maintaining efficacy. The vaccine lacks the B5R protein, which contributes to its attenuation. LC16m8 generates neutralizing antibody titers against multiple poxviruses—including vaccinia, monkeypox (mpox), and variola major—and elicits broad T-cell responses. It is minimally replicating in humans and has been licensed for use in Japan for both smallpox and mpox prevention. Clinical trials have demonstrated robust immunogenicity with fewer adverse effects than older vaccines, making it suitable for targeted vaccination of at-risk groups such as those with well-controlled HIV infection[1][2][3][4][5][6].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on lc16m8.