Key Insights

Highlights

Success Rate

100% trial completion (above average)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 30/100

Termination Rate

0.0%

0 terminated out of 22 trials

Success Rate

100.0%

+13.5% vs benchmark

Late-Stage Pipeline

36%

8 trials in Phase 3/4

Results Transparency

33%

5 of 15 completed with results

Key Signals

5 with results100% success

Data Visualizations

Phase Distribution

17Total
Not Applicable (2)
P 1 (5)
P 2 (2)
P 3 (6)
P 4 (2)

Trial Status

Completed15
Recruiting4
Not Yet Recruiting1
Unknown1
Withdrawn1

Trial Success Rate

100.0%

Benchmark: 86.5%

Based on 15 completed trials

Clinical Trials (22)

Showing 20 of 20 trials
NCT07281599Not ApplicableRecruiting

Evaluation of the Q-Pad hrHPV Test System for Identifying Precancer

NCT07244315Completed

Cervical Cancer Screening of Postmenopausal Women in Low- and Middle-income Countries Using HPV Self-sampling and Triage by Genotyping and Cytology

NCT07081334Phase 1CompletedPrimary

A Phase 1 Study of PV-001 9-valent Human Papillomavirus(HPV) Vaccine

NCT00733122Phase 3WithdrawnPrimary

Tolerability and Immunogenicity of Gardasil in Females Between 16 and 23 Years of Age in India (V501-034)

NCT06672653Phase 1Not Yet Recruiting

Tolerance and Effectiveness of C14 on HPV Infection

NCT05027776Phase 3RecruitingPrimary

Immunogenicity and Safety of Quadrivalent HPV Vaccine in Healthy Chinese Female Subjects Aged 9 to 19 Years

NCT04895020Phase 3RecruitingPrimary

Immunobridging Study of 9-valent Human Papillomavirus Recombinant Vaccine in Chinese Females Aged 9 to 19 Years

NCT05371353RecruitingPrimary

Immune Persistence After the Whole Vaccination Shcedule With Recombination Quadrivalent HPV Vaccine

NCT05372016Phase 3CompletedPrimary

Evaluate the Immunogenicity and Safety of 9-valent HPV Recombinant Vaccine in Chinese Healthy Females

NCT00682812Not ApplicableCompletedPrimary

Significance of the High-risk Hpv Viral Load

NCT03900572Phase 1CompletedPrimary

A Study of Safety and Primary Immunogenicity of 9-valent HPV Recombinant Vaccine

NCT00943722Phase 3Completed

A Study of V503 (A Multivalent Human Papillomavirus [HPV] L1 Virus-Like Particle [VLP] Vaccine) in Preadolescents and Adolescents (V503-002)

NCT00956553Phase 4CompletedPrimary

Reactogenicity Study of Cervarix and Gardasil in UK Adolescent Girls

NCT00834106Phase 3CompletedPrimary

Prevention of Human Papillomavirus (HPV) in 20 to 45 Year Old Chinese Women (V501-041)

NCT03085381Phase 1CompletedPrimary

A Phase I Study of Quadrivalent HPV Recombinant Vaccine

NCT01086709Completed

Crossover Vaccination of Women Previously Randomized Into Protocol 04-C-N191

NCT00411749Phase 2CompletedPrimary

V501 Immunogenicity Study in Females Age 9 to 17 Years (V501-028)

NCT00378560Phase 2CompletedPrimary

V501 Efficacy Study in Women Aged 18 to 26 (V501-027)

NCT00635830Phase 1CompletedPrimary

An Open-Label, Single Dose Safety Study of Quadrivalent HPV Vaccine in Chinese Female Subjects (V501-035)

NCT00847340Completed

Human Papillomavirus (HPV) Genotypes in Genital Warts in Colombian Population

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