Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Diphtheria toxoid + tetanus toxoid + acellular pertussis is a trivalent combination vaccine used for active immunization against diphtheria, tetanus, and pertussis. It is composed of inactivated toxins (toxoids) from *Corynebacterium diphtheriae* and *Clostridium tetani*, along with purified components of *Bordetella pertussis*. The acellular pertussis component typically includes pertussis toxoid (PT) and filamentous haemagglutinin (FHA), and may also contain pertactin (PRN) and fimbriae (FIM). There are two primary formulations: **DTaP**, which contains higher concentrations of antigens for the initial pediatric series in infants and children up to 6 years of age; and **Tdap** (or dTpa), which contains reduced amounts of diphtheria and pertussis antigens for booster doses in adolescents, adults, and pregnant women. The vaccine is typically adsorbed onto an aluminum-based adjuvant to enhance the immune response. Major developers and manufacturers include GSK, Sanofi, and Mitsubishi Tanabe Pharma.
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 diphtheria toxoid + tetanus toxoid + acellular pertussis.