Clinical trial
A Registry-Based Extension of Protocol V503-001 in Countries With Centralized Cervical Cancer Screening Infrastructures to Evaluate the Long-Term Effectiveness, Immunogenicity, and Safety of Multivalent Human Papillomavirus (HPV) L1 Virus-Like Particle (VLP) Vaccine as Administered to 16- to 26- Year-Old Women
NCT02653118 is registered in ClinicalTrials.gov with Merck Sharp & Dohme LLC as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Registry-Based Extension of Protocol V503-001 in Countries With Centralized Cervical Cancer Screening Infrastructures to Evaluate the Long-Term Effectiveness, Immunogenicity, and Safety of Multivalent Human Papillomavirus (HPV) L1 Virus-Like Particle (VLP) Vaccine as Administered to 16- to 26- Year-Old Women
- Lead sponsor
- Merck Sharp & Dohme LLC
- Phase
- Observational
- Overall status
- Active, not recruiting
- Start date
- January 22, 2016
- Completion date
- January 1, 2040
- Enrollment
- 4,453 (estimated)
- Sites
- Not reported
Conditions
As the registry lists them; a condition with its own page is linked.
cervical cancer, genital warts, human papillomavirus infection, vaginal cancer, vulvar cancer