Immunobridging Study of 9- Valent Human Papillomavirus (9vHPV) Vaccine (V503) in Chinese Females 9 to 45 Years of Age (V503-024)
A Phase 3 Open-Label Clinical Trial to Study the Immunogenicity and Safety of 9- Valent Human Papillomavirus (HPV) L1 Virus-Like Particle (VLP) Vaccine (V503) in Chinese Females 9 to 45 Years of Age
Sponsor: Merck Sharp & Dohme LLC
A PHASE3 clinical study on Papillomavirus Infections, this trial is completed. The trial is conducted by Merck Sharp & Dohme LLC and has accumulated 18 data snapshots since 2019. Infectious disease trials contribute critical data for public health response and treatment development.
Status Flow
Change History
18 versions recorded-
Apr 2025 — Present [monthly]
Completed PHASE3
Status: Active Not Recruiting → Completed
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Feb 2025 — Apr 2025 [monthly]
Active Not Recruiting PHASE3
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Sep 2024 — Feb 2025 [monthly]
Active Not Recruiting PHASE3
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Jul 2024 — Sep 2024 [monthly]
Active Not Recruiting PHASE3
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Feb 2023 — Jul 2024 [monthly]
Active Not Recruiting PHASE3
▶ Show 13 earlier versions
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Sep 2022 — Feb 2023 [monthly]
Active Not Recruiting PHASE3
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Jun 2022 — Sep 2022 [monthly]
Active Not Recruiting PHASE3
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Feb 2021 — Jun 2022 [monthly]
Active Not Recruiting PHASE3
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Jan 2021 — Feb 2021 [monthly]
Active Not Recruiting PHASE3
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Dec 2020 — Jan 2021 [monthly]
Active Not Recruiting PHASE3
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Oct 2020 — Dec 2020 [monthly]
Active Not Recruiting PHASE3
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Sep 2020 — Oct 2020 [monthly]
Active Not Recruiting PHASE3
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Jul 2020 — Sep 2020 [monthly]
Active Not Recruiting PHASE3
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Apr 2020 — Jul 2020 [monthly]
Active Not Recruiting PHASE3
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Nov 2019 — Apr 2020 [monthly]
Active Not Recruiting PHASE3
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Oct 2019 — Nov 2019 [monthly]
Active Not Recruiting PHASE3
Status: Recruiting → Active Not Recruiting
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Jun 2019 — Oct 2019 [monthly]
Recruiting PHASE3
Status: Not Yet Recruiting → Recruiting
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May 2019 — Jun 2019 [monthly]
Not Yet Recruiting PHASE3
First recorded
Apr 2019
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- Merck Sharp & Dohme LLC
For direct contact, visit the study record on ClinicalTrials.gov .