drugset / Trial / NCT05104125
Study to Evaluate the Safety and Efficacy of ASC40 in Subjects With Moderate to Severe Acne Vulgaris
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Denifanstat | Small molecule | 25 mg | Oral |
| Subject | Denifanstat | Small molecule | 50 mg | Oral |
| Subject | Denifanstat | Small molecule | 75 mg | Oral |