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Study identifier: NCT07378527 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Study of the Efficacy and Safety of ICP-332 in Participants With Chronic Spontaneous Urticaria

Condition: Chronic Spontaneous Urticaria (CSU)  ·  Sponsor: Beijing InnoCare Pharma Tech Co., Ltd.

PhasePhase 2/Phase 3
Planned participants344
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

The purpose of this study is to compare the efficacy and safety of ICP-332 in moderate to severe chronic spontaneous urticaria subjects inadequately controlled by second generation H1-antihistamines

This description comes directly from the study's public registry record.

Talk to the study team

Jianzhong Zhang  ·  +86-010-88325474  ·  rmzjz@126.com

Always discuss trial participation with your own doctor first.

Locations (30)

Bengbu Medical University First Affiliated HospitalBengbu, Anhui, ChinaNot Yet Recruiting
The Second Affiliated Hospital of Wannan Medical CollegeWuhu, Anhui, ChinaNot Yet Recruiting
Peking University People's HospitalBeijing, Beijing Municipality, ChinaRecruiting
Beijing Tongren Hospital, Capital Medical UniversityBeijing, Beijing Municipality, ChinaNot Yet Recruiting
The First Affiliated Hospital of Chongqing Medical UniversityChongqing, Chongqing Municipality, ChinaNot Yet Recruiting
Chongqing Traditional Chinese Medicine HospitalChongqing, Chongqing Municipality, ChinaNot Yet Recruiting
First Affiliated Hospital of Fujian Medical UniversityFuzhou, Fujian, ChinaNot Yet Recruiting
Dermatology Hospital of Southern Medical UniversityGuangzhou, Guangdong, ChinaNot Yet Recruiting
The Second Hospital of Hebei Medical UniversityShijiazhuang, Hebei, ChinaNot Yet Recruiting
The Second Affiliated Hospital of Henan University of Science and TechnologyLuoyang, Henan, ChinaNot Yet Recruiting
Henan Provincial People's HospitalZhengzhou, Henan, ChinaNot Yet Recruiting
Jingzhou Central HospitalJingzhou, Hubei, ChinaNot Yet Recruiting

+ 18 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT07378527