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Clinical Trial Summary

This study is a randomized, double-blind, placebo-controlled, multicenter clinical trial of about 36 subjects with moderate to severe Chronic Spontaneous Urticaria.


Clinical Trial Description

Successfully screened subjects will be randomized in a ratio of 1:1:1. After a 4-week screening period (day -28-0), subjects will be randomly assigned to treatment for 12 weeks. Clinical Urticaria Activity Score (UAS), dermatological Quality of Life Index (DLQI), physical exams and Laboratory tests will be performed at baseline, the end of weeks 4, 8 and 12 respectively. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05373355
Study type Interventional
Source Hangzhou Highlightll Pharmaceutical Co., Ltd
Contact
Status Completed
Phase Phase 1
Start date May 10, 2022
Completion date September 7, 2023

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