Key Insights

Highlights

Success Rate

100% trial completion (above average)

Clinical Risk Assessment

Based on trial outcomes

Low Risk

Score: 27/100

Termination Rate

0.0%

0 terminated out of 12 trials

Success Rate

100.0%

+13.4% vs benchmark

Late-Stage Pipeline

25%

3 trials in Phase 3/4

Results Transparency

40%

2 of 5 completed with results

Key Signals

2 with results100% success

Data Visualizations

Phase Distribution

10Total
Not Applicable (2)
Early P 1 (1)
P 1 (3)
P 2 (1)
P 3 (1)
P 4 (2)

Trial Status

Recruiting6
Completed5
Active Not Recruiting1

Trial Success Rate

100.0%

Benchmark: 86.6%

Based on 5 completed trials

Clinical Trials (12)

Showing 12 of 12 trials
NCT07729579Phase 1RecruitingPrimary

An Open-Label Pharmacokinetic Study for Patients With Actinic Keratosis on the Upper Extremities or the Face

NCT07340697Phase 1Active Not RecruitingPrimary

Evaluate RLS-1496 Topical Cream for Actinic Keratosis

NCT07657988RecruitingPrimary

Outcomes Associated With Tirbanibulin for Large Field Application on the Face in the U.S (CLEAR)

NCT07286318Early Phase 1Recruiting

A Randomized Controlled Trial of Topical 5% Niacinamide for Skin Cancer Prevention in Transplant Recipients

NCT07335003Not ApplicableRecruitingPrimary

Study of the Photoprotection and Prevention of Actinic Damage With Anthelios Fluide 100 KA+ UVMune 400 in Patients With Multiple Actinic Keratoses

NCT07318675Phase 1RecruitingPrimary

A Phase Ib Study of HW211026 Ointment in Patients With Actinic Keratosis.

NCT07290959Not ApplicableCompletedPrimary

Indoor Daylight Photodynamic Therapy is an Effective, First-line Treatment for AK, But Its Feasibility is Limited by the Time Required for the Illumination (2 Hours). Our Objective Was to Evaluate the Efficacy of Idl-PDT With an Illumination Time of 1 Hour Versus 2 Hours in the Treatment of Scalp AK

NCT06648447RecruitingPrimary

Investigation of the Efficacy and Tolerability of Topical Applied Tirbanibulin on Actinic Keratoses With Downward-directed Proliferation Patterns

NCT01926496Phase 4CompletedPrimary

Risk of Squamous Cell Carcinoma on Skin Areas Treated With Ingenol Mebutate Gel, 0.015% and Imiquimod Cream, 5%

NCT02406014Phase 4CompletedPrimary

Efficacy and Safety of Ingenol Mebutate Gel 0.015% Compared to Diclofenac Sodium Gel 3% in Subjects With Actinic Keratoses on the Face or Scalp

NCT03727074Phase 3CompletedPrimary

Bioequivalence Study to Compare Sol-Gel Technologies' 5-FU Cream With Efudex® (5-FU) Cream

NCT03116698Phase 2CompletedPrimary

A Study to Evaluate Two Concentrations of DFD-07 Cream, in Subjects With Actinic Keratosis (AK) of the Face and/or Scalp Over a 12-week Treatment Period

Showing all 12 trials

Research Network

Activity Timeline