Products V501
V501 Phase 3 Completed 📈 Rising Prevention of HPV Types 16- and 18-related Cervical Cancer, Cervical Intraepithelial Neoplasia (CIN) 1/2/3, and Cervical Adenocarcinoma in Situ
Prevention of HPV Types 16- and 18-related Cervical Cancer, Cervical Intraepithelial Neoplasia (CIN) 1/2/3, and Cervical Adenocarcinoma in Situ
Aug 31, 2018 → Oct 30, 2023
About V501 V501 is a phase 3 stage product being developed by Merck for Prevention of HPV Types 16- and 18-related Cervical Cancer, Cervical Intraepithelial Neoplasia (CIN) 1/2/3, and Cervical Adenocarcinoma in Situ. The current trial status is completed. This product is registered under clinical trial identifier NCT03493542. Target conditions include Prevention of HPV Types 16- and 18-related Cervical Cancer, Cervical Intraepithelial Neoplasia (CIN) 1/2/3, and Cervical Adenocarcinoma in Situ.
Clinical Trials (3) NCT ID Phase Status Start Completion Indication NCT03493542 Phase 3 Completed Aug 31, 2018 Oct 30, 2023 Prevention of HPV Types 16- and 18-related Cervical Cancer, Cervical Intraepithelial Neoplasia (CIN) 1/2/3, and Cervical Adenocarcinoma in Situ NCT02576054 Phase 3 Completed Nov 20, 2015 Aug 8, 2018 Anogenital Human Papilloma Virus Infection NCT01544478 Approved Completed Nov 25, 2011 Aug 27, 2016 Cervical Cancer
Competing Products 20 competing products in Prevention of HPV Types 16- and 18-related Cervical Cancer, Cervical Intraepithelial Neoplasia (CIN) 1/2/3, and Cervical Adenocarcinoma in Situ
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