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Clinical Trial Summary

This is a multicenter, randomized, double-blind, placebo-controlled Phase III study to evaluate the efficacy and safety of ASC40 (Denifanstat) tablets compared to placebo in the treatment of patients with moderate to severe acne vulgaris. The proposed plan for this trial is to enroll subjects who are 18-40 years of age (including borderline values), with a diagnosis of moderate to severe acne vulgaris, and an Investigator's Global Assessment (IGA) graded as moderate (grade 3) or severe (grade 4). 480 subjects were planned to be enrolled in the trial and placebo groups, with all subjects randomly assigned in a 1:1 ratio to receive either ASC40 (denifanstat) tablets dose 1 or placebo, administered orally once daily (taken after dinner) for 12 weeks. There will be a total of 6 visits for screening and follow-up. The tests required by the program included routine blood tests, blood biochemistry, lipid profile, pregnancy test and urine routine, etc..


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06192264
Study type Interventional
Source Ascletis Pharmaceuticals Co., Ltd.
Contact Leihong Xiang, Doctor
Phone 021-52888045
Email flora_xiang@vip.163.com
Status Recruiting
Phase Phase 3
Start date January 23, 2024
Completion date March 9, 2025

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