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Study identifier: NCT07047612 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

ICP-332 in Subjects With Non-segmental Vitiligo

Condition: Non Segmental Vitiligo  ·  Sponsor: Beijing InnoCare Pharma Tech Co., Ltd.

PhasePhase 2/Phase 3
Planned participants603
Who can joinAll sexes, 12 Years to 75 Years
Healthy volunteersNo

About this study

This a phase II/III randomized, double-blind, placebo-controlled, parallel group, adaptive design, multi-center study to evaluate the efficacy and safety of ICP-332 in subjects with non-segmental vitiligo。The study consisted an phase 2 part and an phase 3 part.

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

Talk to the study team

Flora Xiang, Doctor  ·  021-52887775  ·  flora_xiang@vip.163.com

Always discuss trial participation with your own doctor first.

Locations (45)

The First Affiliated Hospital of Wannan Medical CollegeWuhu, Anhui, ChinaNot Yet Recruiting
The Second Affiliated Hospital of Wannan Medical CollegeWuhu, Anhui, ChinaNot Yet Recruiting
Peking University Third HospitalBeijing, Beijing Municipality, ChinaNot Yet Recruiting
Beijing Chao-yang Hospital,Capital Medical UniversityBeijing, Beijing Municipality, ChinaNot Yet Recruiting
Beijing Tongren HospitalBeijing, 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, ChinaRecruiting
Union Hospital affiliated to Fujian MedicalFuzhou, Fujian, ChinaNot Yet Recruiting
The First Affiliated Hospital of Fujian MedicalFuzhou, Fujian, ChinaNot Yet Recruiting
Sun Yat-sen Memorial Hospital,Sun Yat-sen UniversityGuangzhou, Guangdong, ChinaNot Yet Recruiting
Deramatology Hospital of Southern Medical UnivercityGuangzhou, Guangdong, ChinaNot Yet Recruiting
Nanfang HospitalGuangzhou, Guangdong, ChinaNot Yet Recruiting

+ 33 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT07047612