drugset / Trial / NCT05104125

Study to Evaluate the Safety and Efficacy of ASC40 in Subjects With Moderate to Severe Acne Vulgaris

NCT05104125

Phase 2 Completed 180 enrolled Ascletis Pharmaceuticals Co., Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a phase2, randomized, double-blind, multi-center, multi-dose and placebo parallel controlled design. The subjects in the study group were given double-blind drugs, and they were taken (orally) after dinner every day according to the requirements of clinical trial scheme.

Timeline

Start
2022-01-12
Primary completion
2023-04-10
Completion
2023-04-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Denifanstat Small molecule 25 mg Oral
Subject Denifanstat Small molecule 50 mg Oral
Subject Denifanstat Small molecule 75 mg Oral

Indications