Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Tetadif is an adsorbed tetanus-diphtheria toxoid (Td) vaccine with reduced-dose diphtheria content, developed and manufactured by the Bulgarian state-owned company BB-NCIPD Ltd (BulBio). The vaccine is a combination biologic containing purified tetanus and diphtheria toxoids adsorbed onto an aluminum hydroxide gel adjuvant, with thiomersal included as a preservative. It is specifically formulated for the active immunization of adults and children aged 7 years and older against tetanus and diphtheria. The vaccine works by inducing the production of neutralizing antibodies against the tetanus toxin produced by *Clostridium tetani* and the diphtheria toxin produced by *Corynebacterium diphtheriae*. Tetadif has been WHO prequalified since 2006 and serves as a significant supplier for global immunization programs through UNICEF.
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 Tetadif.