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Clinical Trial Summary

This is a multicenter, open-label study designed to determine the long-term safety of ASC40 (Denifanstat) tablets in patients with moderate to severe acne vulgaris enrolled in the ASC40-303 Phase III study. All subjects are eligible for study eligibility screening after enrollment in ASC40-303 Phase III study, and all eligible subjects with moderate to severe acne vulgaris will receive ASC40 (Denifanstat) tablets after signing informed consent. The investigational drug will be administered orally once daily (QD) for up to 40 weeks. There will be a total of 7 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 NCT06248008
Study type Interventional
Source Ascletis Pharmaceuticals Co., Ltd.
Contact Xiang Leihong, Doctor
Phone 021-52888045
Email flora_xiang@vip.163.com
Status Not yet recruiting
Phase Phase 3
Start date April 24, 2024
Completion date March 9, 2026

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