RecruitingPHASE1, PHASE2NCT07017725
A Dose-escalation Study Followed by a Dose Optimal Study to Evaluate the Safety and Efficacy of CID-103 in Adults With Chronic Immune Thrombocytopenia
Studying Autoimmune thrombocytopenia
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- CASI Pharmaceuticals, Inc.
- Principal Investigator
- Junping ChenCASI pharmaceutical, Inc
- Intervention
- CID-103(drug)
- Enrollment
- 75 enrolled
- Eligibility
- 18-65 years · All sexes
- Timeline
- 2025 – 2026
Study locations (6)
- North China University of Science and Technology Affiliated Hospital, Tangshan, Hebei, China
- Henan Cancer Hospital, Zhengzhou, Henan, China
- The First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, China
- Qilu Hospital of Shandong University, Jinan, Shandong, China
- Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences, Tianjin, Tianjin Municipality, China
- The Second Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, China
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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