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Clinical Trial Summary

The primary objective of this study is to evaluate the durability of protection of Recombinant Human Papillomavirus Bivalent (Types 16,18) Vaccine administered in females aged 18-45 years.


Clinical Trial Description

This is a follow-up study that is based on phase III clinical study of a recombinant human papillomavirus 16/18 bivalent vaccine in females aged 18-45 years (Unique Protocol ID: HPV-PRO-003, Identifiers: NCT01735006). The investigators will recruit people who have participated in phase III clinical study on Hebei Province before and to evaluate the durability of protection of the bivalent HPV vaccine on 90m and 114m after dose 1. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04969445
Study type Observational
Source Xiamen University
Contact Chao Zhao, Doctor
Phone +86-010-88324354
Email zhaochaocjr@163.com
Status Recruiting
Phase
Start date March 30, 2021
Completion date January 2024

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