CompletedPHASE2, PHASE3NCT04428255
A Clinical Study on the Efficacy and Safety of HBM9161 in Patients With ITP
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
- Harbour BioMed (Guangzhou) Co. Ltd.
- Principal Investigator
- Renchi YangHematology hospital, Chinese academy of medical sciences
- Intervention
- HBM9161 Dose A(drug)
- Enrollment
- 36 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2020 – 2023
Study locations (1)
- Hematology hospital, Chinese academy of medical sciences, Tianjin, Tianjin Municipality, 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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