A Phase 3 Randomized, Double-Blinded, Controlled With GARDASIL Efficacy, Immunogenicity and Safety Study of V503 [a 9-Valent HPV Vaccine] in Chinese Women 20 to 45 Years of Age
Latest Information Update: 16 May 2022
At a glance
- Drugs V 503 (Primary)
- Indications Adenocarcinoma; Cervical cancer; Cervical intraepithelial neoplasia; Human papillomavirus infections
- Focus Adverse reactions; Pharmacodynamics; Registrational; Therapeutic Use
- Sponsors Merck & Co; Merck Sharp & Dohme
- 16 Nov 2020 Planned End Date changed from 1 Feb 2027 to 31 Mar 2028.
- 16 Nov 2020 Planned primary completion date changed from 1 Feb 2027 to 31 Mar 2028.
- 19 Jan 2020 Status changed from recruiting to active, no longer recruiting.