A Phase 1 Randomized, Open Label, Active-Controlled, Dose Escalation, Multi-center Study to Evaluate the Safety, Tolerability, and Immunogenicity of an Investigational Tetanus/Diphtheria/Pertussis Booster Vaccine (Tdap-1018) Compared to a Licensed Tdap Vaccine in Healthy Volunteers Between 10 and 22 Years of Age
Latest Information Update: 16 Nov 2022
At a glance
- Drugs Adjuvanted pertussis vaccine-Dynavax Technologie's/Serum Institute of India (Primary)
- Indications Diphtheria; Pertussis; Tetanus
- Focus Adverse reactions
- Sponsors Dynavax Technologies
- 03 Nov 2022 According to a Dynavax Technologies media release, data from this study were presented at the ID Week 2022.
- 04 Aug 2022 According to a Dynavax Technologies media release, the company previously reported interim adult data from an on-going Phase 1 clinical trial evaluating the Company's adjuvanted Tdap vaccine candidate demonstrated it was well tolerated without safety concerns with immunogenicity data supporting continued advancement.
- 04 Aug 2022 According to a Dynavax Technologies media release, adolescent data from this trial is anticipated in the fourth quarter of 2022.