Key Insights

Highlights

Success Rate

100% trial completion (above average)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 40/100

Termination Rate

0.0%

0 terminated out of 14 trials

Success Rate

100.0%

+13.5% vs benchmark

Late-Stage Pipeline

14%

2 trials in Phase 3/4

Results Transparency

0%

0 of 8 completed with results

Key Signals

100% success

Data Visualizations

Phase Distribution

9Total
Not Applicable (5)
P 1 (1)
P 2 (1)
P 3 (1)
P 4 (1)

Trial Status

Completed8
Unknown4
Recruiting1
Not Yet Recruiting1

Trial Success Rate

100.0%

Benchmark: 86.5%

Based on 8 completed trials

Clinical Trials (14)

Showing 14 of 14 trials
NCT07545746Phase 2Not Yet Recruiting

Adjuvant 5-Fluorouracil Following Thermal Ablation to Improve HPV Treatment Outcomes in Women With HIV in Kenya

NCT07020130CompletedPrimary

Risk Factors,PREvention and OutComes for CI-AKI in PatientS undErgoing PCI (PRECISE)

NCT06261879Not ApplicableRecruiting

Non-invasive Biomarker Discovery for Pre-cervical or/and Cervical Cancer--ACTN4 and Other Biomarkers in Menstrual Blood

NCT05580341Phase 3Unknown

Phase III Study Comparing the Immunogenicity of 9-valent HPV Recombinant Vaccine and Gardasil-9

NCT04809727Not ApplicableCompletedPrimary

Histopathological Findings in Symptomatizing Patients After Supracervical Hysterectomy

NCT00339989Completed

Cervical Cancer Early Endpoints and Determinants

NCT03239223Phase 1Completed

Study of Topical ABI-1968 in Subjects With Precancerous Cervical Lesions From Human Papillomavirus (HPV) Infection

NCT03872739Not ApplicableUnknownPrimary

To Compare Intravenous and Oral Hydration of the Prevention for CIN in Elderly Patients Undergoing Intravenous CECT

NCT03791606CompletedPrimary

Risk Factors,PREvention and OutComes for CI-AKI in PatientS undErgoing PCI at Intensive Care Unit(PRECISE-ICU)

NCT02363244CompletedPrimary

Pap and HPVDNA Before and After Acetic Acid

NCT02116920UnknownPrimary

HPV E6/E7 mRNA Versus HPV DNA as Triage for Cervical Cancer Screening

NCT01836588Not ApplicableUnknownPrimary

New Gentle Biopsy Method of Cervix Lesions Using Superficial Curettage/Protocol ID: CX-CUR

NCT01766284Not ApplicableCompleted

Study of the Diagnostic Efficacy of "Real Time" Niris 1300e Optical Coherence Tomography (OCT) Imaging System in the Management of Pre-invasive and Invasive Neoplasia of the Uterine Cervix

NCT00289029Phase 4CompletedPrimary

A Study of Two Iodinated Contrast Agents in Renally Impaired Patients Undergoing Cardiac Angiography

Showing all 14 trials

Research Network

Activity Timeline