Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Gardasil 9 + QDENGA refers to the co-administration of two distinct vaccines: Takeda's tetravalent dengue vaccine (TAK-003, brand name QDENGA) and Merck's 9-valent human papillomavirus (HPV) vaccine (Gardasil 9). TAK-003 is a live-attenuated vaccine based on a dengue virus serotype 2 (DENV-2) backbone, with chimeric strains expressing surface antigens for DENV-1, DENV-3, and DENV-4, providing protection against all four dengue serotypes. Gardasil 9 is a recombinant vaccine composed of virus-like particles (VLPs) targeting nine HPV types (6, 11, 16, 18, 31, 33, 45, 52, and 58). A Phase 3 clinical trial (NCT04313244) conducted in Thailand evaluated the safety and immunogenicity of co-administering these vaccines in healthy adolescents aged 9 to 14 years. The study demonstrated that the immune response to both vaccines was non-inferior when administered together compared to separate administration, with a safety profile consistent with the individual vaccines.
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 Gardasil 9 + QDENGA.