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Clinical Trial Summary

The goal of this clinical trial is to evaluate the effectiveness of QY101 ointment in adult patients with plaque psoriasis (2-20% BSA).


Clinical Trial Description

Participants will be stratified and randomly assigned to trial groups two (Test group 1:0.3%; Test group 2:1.0%, 60 patients per group) or placebo group (40 patients) according to the ratio of 3:3:2 and BSA (BSA < 10% or BSA ≥ 10%) . All groups will be receive with QY101 ointment or placebo, treatment for twice daily (BID) for 12 weeks; All subjects are required to take part in visit at 2, 4, 6, 8 and 12 weeks, they were followed up for efficacy assessment, safety examination and pharmacokinetics samples collection (with week 8 as the primary efficacy endpoint), and safety follow-up was administered 28 ± 7 days after the last dose via telephone . ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06170840
Study type Interventional
Source E-nitiate Biopharmaceuticals (Hangzhou) Co., Ltd.
Contact Xiaoyong Man, Doctor
Phone +86 1360051 6219
Email manxy@zju.edu.cn
Status Recruiting
Phase Phase 2
Start date May 17, 2023
Completion date April 30, 2024

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