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Not Yet RecruitingNCT07492303

A Phase I Clinical Trial of Absorbed Acellular Pertussis (Two-Component) Diphtheria-Tetanus Combined Vaccine (For Adults and Adolescents)

A Phase I Clinical Trial to Evaluate the Safety and Immunogenicity of Different Doses of Adsorbed Acellular Pertussis (Two-component) Diphtheria-tetanus Combined Vaccine (for Adults and Adolescents) in People Aged 10 Years and Older in a Randomized, Blinded, Placebo-controlled Manner

Status
Not Yet Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
96 (estimated)
Sponsor
Changchun BCHT Biotechnology Co. · Industry
Sex
All
Age
10 Years
Healthy volunteers
Accepted

Summary

the safety and tolerability of different dosages of adsorbed acellular pertussis (two-component) diphtheria-tetanus combined vaccine

Detailed description

14day and 30 days after exemption

Conditions

Interventions

TypeNameDescription
BIOLOGICALTdap vaccineintramuscular injection only, and the preferred inoculation site is the deltoid muscle of the upper arm.

Timeline

Start date
2026-04-20
Primary completion
2026-07-10
Completion
2027-08-20
First posted
2026-03-25
Last updated
2026-03-25

Source: ClinicalTrials.gov record NCT07492303. Inclusion in this directory is not an endorsement.