Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
tetanus toxoid reduced diphtheria toxoid acellular pertussis-Sanofi Pasteur, a Sanofi Company-dengue refers to the co-administration or combined study of Sanofi Pasteur's Tdap vaccine (Adacel) and its tetravalent dengue vaccine (Dengvaxia/CYD-TDV). Adacel is a sterile isotonic suspension of tetanus and diphtheria toxoids and adsorbed acellular pertussis antigens, used for booster immunization. Dengvaxia is a live-attenuated chimeric vaccine using a yellow fever 17D virus backbone to express the pre-membrane and envelope proteins of the four dengue virus serotypes (DENV-1, 2, 3, and 4). This combination was specifically evaluated in Phase 2 clinical trials (such as NCT00842530) to determine the safety and immunogenicity of simultaneous or sequential administration in pediatric populations in endemic regions.
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 tetanus toxoid reduced diphtheria toxoid acellular pertussis-Sanofi Pasteur, a Sanofi Company-dengue.