Safety and Immunogenicity Study of the Recombinant Human Papillomavirus Virus Type 6/11 Bivalent Vaccine
A Phase I Randomized, Double-Blinded, Placebo Controlled Study to Evaluate the Safety and Immunogenicity of the Recombinant (E.Coli) Human Papillomavirus Type 6/11 Bivalent Vaccine in Healthy Volunteers Aged 18-55 Years
Sponsor: Beijing Wantai Biological Pharmacy Enterprise Co., Ltd.
This PHASE1 trial investigates Condylomata Acuminata and is currently completed. Beijing Wantai Biological Pharmacy Enterprise Co., Ltd. leads this study, which shows 12 recorded versions since 2015 — indicating substantial longitudinal coverage. The change history captured here reflects the iterative nature of clinical trial conduct.
Status Flow
Change History
12 versions recorded-
Sep 2024 — Present [monthly]
Completed PHASE1
-
Jul 2024 — Sep 2024 [monthly]
Completed PHASE1
-
Jun 2022 — Jul 2024 [monthly]
Completed PHASE1
Status: Active Not Recruiting → Completed
-
Mar 2022 — Jun 2022 [monthly]
Active Not Recruiting PHASE1
-
Jan 2021 — Mar 2022 [monthly]
Active Not Recruiting PHASE1
▶ Show 7 earlier versions
-
Oct 2020 — Jan 2021 [monthly]
Active Not Recruiting PHASE1
-
May 2020 — Oct 2020 [monthly]
Active Not Recruiting PHASE1
-
Jan 2020 — May 2020 [monthly]
Active Not Recruiting PHASE1
-
Sep 2018 — Jan 2020 [monthly]
Active Not Recruiting PHASE1
Status: Unknown Status → Active Not Recruiting
-
Jun 2018 — Sep 2018 [monthly]
Unknown Status PHASE1
-
Feb 2018 — Jun 2018 [monthly]
Unknown Status PHASE1
Status: Active Not Recruiting → Unknown Status
-
Jan 2017 — Feb 2018 [monthly]
Active Not Recruiting PHASE1
First recorded
Mar 2015
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- Beijing Wantai Biological Pharmacy Enterprise Co., Ltd.
- Jun Zhang
- Xiamen Innovax Biotech Co., Ltd
For direct contact, visit the study record on ClinicalTrials.gov .
Study Locations
No location information available.