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Clinical Trial Summary

The purpose of this study is to evaluate the immunogenicity and safety of co-immunization with recombinant human papillomavirus bivalent (Types 16,18) vaccine (Escherichia coli) and Hepatitis E vaccine (Escherichia coli)


Clinical Trial Description

Cecolin is the first Chinese domestic human papillomavirus (HPV) vaccine. Cecolin is designed to protect against HPV types 16 and 18, the most common virus types that lead to cervical cancer. Hecolin is the first prophylactic vaccine against hepatitis E virus (HEV). The purpose of this study is to evaluate the immunogenicity and safety of co-immunization with Cecolin and Hecolin. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05415345
Study type Interventional
Source Xiamen Innovax Biotech Co., Ltd
Contact
Status Active, not recruiting
Phase Phase 4
Start date October 25, 2021
Completion date June 10, 2023

See also
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Completed NCT02733068 - A Phase III Study of Human Papillomavirus (HPV)-16/18 Vaccine. Phase 3
Completed NCT02558803 - HPV Vaccination: Evaluation of Reminder Prompts for Doses 2 & 3 N/A
Completed NCT02551887 - HPV Vaccination: An Investigation of Physician Reminders and Recommendation Scripts N/A
Active, not recruiting NCT05669911 - Development of a Self-collection Device for Cervical Cancer Screening N/A
Active, not recruiting NCT05279248 - The Immunogenicity and Safety of the Vaccination of Human Papillomavirus Vaccine and Measles-Mumps-Rubella Vaccine Phase 4