Clinical Trials Directory

Trials / Unknown

UnknownNCT03659110

Post-Approval Safety Monitoring Program to Assess the Safety Profile of GARDASIL in China Usual Practice

Status
Unknown
Phase
Study type
Observational
Enrollment
1,000 (estimated)
Sponsor
Beijing Chaoyang District Centre for Disease Control and Prevention · Academic / Other
Sex
Female
Age
20 Years – 45 Years
Healthy volunteers
Accepted

Summary

This is a post-Approval Safety Monitoring Program to assess the safety profile of GARDASIL in china usual practice.

Conditions

Interventions

TypeNameDescription
BIOLOGICALHPV 41000 subjects will be received the HPV 4 vaccine

Timeline

Start date
2018-10-01
Primary completion
2021-07-30
Completion
2021-12-30
First posted
2018-09-06
Last updated
2018-09-27

Source: ClinicalTrials.gov record NCT03659110. Inclusion in this directory is not an endorsement.