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Not Yet RecruitingNCT06961721

A Multicenter, Randomized, Double-Blind, Placebo-Controlled Phase IV Clinical Trial to Evaluate the Immunogenicity and Safety of a Live Attenuated Herpes Zoster Vaccine in Adults Aged 40 Years and Older

Status
Not Yet Recruiting
Phase
Phase 4
Study type
Interventional
Enrollment
600 (estimated)
Sponsor
Changchun BCHT Biotechnology Co. · Industry
Sex
All
Age
40 Years
Healthy volunteers
Accepted

Summary

To evaluate the immunogenicity 42 days after vaccination with the live attenuated herpes zoster vaccine. To evaluate the safety of the live attenuated herpes zoster vaccine.

Conditions

Interventions

TypeNameDescription
BIOLOGICALHerpes Zoster Vaccine, Liveassigned to the vaccine group and placebo group in a 2:1 ratio.
BIOLOGICALPlaceboassigned to the vaccine group and placebo group in a 2:1 ratio.

Timeline

Start date
2025-05-01
Primary completion
2025-07-01
Completion
2025-12-01
First posted
2025-05-08
Last updated
2025-05-08

Source: ClinicalTrials.gov record NCT06961721. Inclusion in this directory is not an endorsement.

A Multicenter, Randomized, Double-Blind, Placebo-Controlled Phase IV Clinical Trial to Evaluate the Immunogenicity and S (NCT06961721) · Clinical Trials Directory