Key Insights

Highlights

Success Rate

82% trial completion

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 52/100

Termination Rate

13.3%

2 terminated out of 15 trials

Success Rate

81.8%

-4.7% vs benchmark

Late-Stage Pipeline

27%

4 trials in Phase 3/4

Results Transparency

0%

0 of 9 completed with results

Key Signals

82% success

Data Visualizations

Phase Distribution

9Total
Not Applicable (2)
Early P 1 (1)
P 2 (2)
P 3 (3)
P 4 (1)

Trial Status

Completed9
Unknown3
Terminated2
Recruiting1

Trial Success Rate

81.8%

Benchmark: 86.5%

Based on 9 completed trials

Clinical Trials (15)

Showing 15 of 15 trials
NCT05463796Recruiting

InAdvance: Surveillance, Prevention, and Interception in a Population at Risk for Cancer

NCT05104099Phase 2CompletedPrimary

Evaluation of New Diagnostic Tool Using Fluorescence to Detect High-grade Vulvar Intraepithelial Neoplasia

NCT02140021Not ApplicableTerminated

Biospecimen Collection and Testing for the Prevalence of Anal Dysplasia and Anal Cancer in Patients With Cervical, Vaginal and Vulvar Dysplasia and Cancer

NCT06297187CompletedPrimary

Cavitronic Ultrasonic Surgical Aspiration (CUSA) Women's Health Study

NCT02735109Not ApplicableTerminated

Interest of the Confocal Microscope in the Diagnosis of Epidermoid Carcinoma of the Vulva and Their Precursors

NCT05045755Unknown

The Durability of Protection and Immuno-persistence Study of a Recombinant HPV 16/18 Bivalent Vaccine in Female

NCT04704908Unknown

Immuno-persistence Study of a Recombinant Human Papillomavirus 16/18 Bivalent Vaccine in Preadolescent Girls (54m)

NCT04969445Unknown

The Durability of Protection Study of a Recombinant HPV 16/18 Bivalent Vaccine in Female

NCT05426148Phase 4Completed

Lot Consistency Clinical Trial of of Recombinant HPV Bivalent Vaccine in 9 to14 Years Old Healthy Female

NCT01861535Phase 3CompletedPrimary

Primary Imiquimod Treatment Versus Surgery for Vulvar Intraepithelial Neoplasia

NCT01735006Phase 3Completed

Efficacy and Immunogenicity Study of Recombinant Human Papillomavirus Bivalent(Type 16/18 )Vaccine

NCT03206255Completed

Immuno-persistence Study of a Recombinant Human Papillomavirus 16/18 Bivalent Vaccine in Preadolescent Girls

NCT02562508Phase 3Completed

A Bridging Study of a Recombinant Human Papillomavirus 16/18 Bivalent Vaccine in Preadolescent Girls

NCT01986725Phase 2Completed

The Impact of the "WOMAN-PRO II Program" on Patients With Vulvar Neoplasia to Minimize Post-surgical Symptom Prevalence

NCT01676792Early Phase 1CompletedPrimary

SR-T100 Gel Efficacy & Safety Study for Vulva Pre-cancerous Lesions & Cutaneous Condyloma

Showing all 15 trials

Research Network

Activity Timeline