Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
CpG 1018-adjuvanted pandemic influenza vaccine (H5N1) is an investigational, monovalent H5N1 influenza vaccine program developed by Dynavax. It presents H5N1 hemagglutinin antigen to induce protective influenza-specific immunity and incorporates Dynavax's CpG 1018, a Toll-like receptor 9 agonist adjuvant intended to amplify innate and adaptive immune responses. Dynavax initiated the program as a pandemic-influenza proof of concept; Part 1 of its randomized Phase 1/2 study enrolled and dosed 101 adults aged 18–49 years in 2025, and a subsequent registered Phase 2 dose-finding study evaluates one- and two-dose intramuscular H5N1 hemagglutinin formulations containing CpG 1018, with some study arms also containing alum. ([biospace.com](https://www.biospace.com/press-releases/dynavax-reports-second-quarter-2025-financial-results))
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 CpG 1018-adjuvanted pandemic influenza vaccine (H5N1).