drugset / Trial / NCT02935036

Efficacy Study in Patients With Acne Vulgaris.

NCT02935036 ↗

Phase 2 Completed 294 enrolled Sun Pharmaceutical Industries, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Safety and efficacy study in patients with acne vulgaris

Timeline

Start
2016-10-03
Primary completion
2017-01-24
Completion
2017-03-21

Outcome

Missed primary endpoint

registry analysis (superiority test); ADPS Topical Product vs Placebo Control; p = 0.5947; LS Mean Difference 1.33; ANOVA NCT02935036 ↗

registry analysis (superiority test); ADPS Topical Product vs Placebo Control; p = 0.2912; LS Mean Difference 2.75; ANOVA NCT02935036 ↗

registry analysis (superiority test); ADPS Topical Product vs Placebo Control; p = 0.6920; Percent difference 2.4; Cochran-Mantel-Haenszel NCT02935036 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject ADPS Unknown — Topical

Indications