Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
The WRAIR Tetravalent Dengue Vaccine (T-DEN) is a live-attenuated vaccine candidate developed by the Walter Reed Army Institute of Research (WRAIR) and the U.S. Army Medical Research and Development Command (USAMRDC). It is designed to provide protection against all four serotypes of the dengue virus (DENV-1, DENV-2, DENV-3, and DENV-4). The vaccine strains were attenuated through serial passage in primary dog kidney (PDK) cells. In specific clinical formulations, such as F17 and F19, Humulin R (regular human insulin) is added to the vaccine diluent as a stabilizer to prevent viral adsorption to the surfaces of vials and syringes. The vaccine is typically administered subcutaneously on a two-dose schedule (0 and 6 months) and aims to elicit a balanced neutralizing antibody response to prevent dengue fever and severe dengue disease.
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 WRAIR Tetravalent Dengue Vaccine.