Tetanus toxoid adsorbed
As of the edition of 20 October 2026, Tetanus toxoid adsorbed is a vaccine component: marketed, first approved in 1999 (US); US protection ended in 2011.
Sources: FDA Orange Book and Purple Book, other approval registers, ClinicalTrials.gov, ChEMBL.
The drug
- Status
- Marketed; latest approval 2004
- Kind
- Vaccine component
- Brand name
- Infanrix Hexa
- First approved
- 9 December 1999 (US)
- Approvals on record
- 4 in 2 regions
- Holder of the most recent approval
- Sanofi; 3 holders in all
- Registered trials
- 1, 0 stopped early
- Disease areas
- Blood and lymph; Cancer; Immune system
US protection
US protection ended in 2011.
US protection ended in 2011, computed as 12 years from the first US licence because FDA publishes no date for this product. The application that gives this date is held by Sanofi. The date is computed, not published.
This is the US only, and it is not the date generics or biosimilars can enter.
The exact date and the listings behind it
In the product1 listing counts towards this date. The exact date and each listing are in the product.
See the exact date and the 1 listing behind itRequest access. Nothing is shown until you do.
Registered trials
| Phase | Trials | Completed | Active | Stopped early |
|---|---|---|---|---|
| Phase 1 | 1 | 1 | 0 | 0 |
| All trials | 1 |