Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
TDEN F17 (Tetravalent Dengue Vaccine F17) is a live-attenuated tetravalent dengue vaccine developed by the Walter Reed Army Institute of Research (WRAIR) in collaboration with GSK, under the U.S. Army Medical Research and Development Command. The vaccine contains four attenuated dengue virus strains representing all four serotypes: DENV-1 (45AZ5), DENV-2 (S16803), DENV-3 (CH53489), and DENV-4 (341750). These strains were obtained from natural infections and attenuated through serial passages in primary dog kidney (PDK) cells. The vaccine is administered as a two-dose regimen given 180 days apart and has been shown to be safe and immunogenic in individuals ranging from 12 months to 50 years of age. The F17 formulation was developed as an optimization of the earlier F17pre formulation to improve neutralizing antibody responses and long-term immunity.
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 TDEN F17.