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Clinical Trial Summary

This project was undertaken to evaluate the efficacy and safety of BTK inhibitor Orelabrutinib for the secondary treatment of adults with primary immune thrombocytopenia (ITP).


Clinical Trial Description

The investigators are undertaking a prospective trial of 10 adults with ITP in China. Orelabrutinib is administered as 50 mg po. qd for 6 weeks. Platelet count, bleeding and other symptoms were evaluated before and after treatment. Adverse events are also recorded throughout the study. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05124028
Study type Interventional
Source Peking University People's Hospital
Contact Xiao-Hui Zhang, MD
Phone 010-88324577
Email zhangxh100@sina.com
Status Not yet recruiting
Phase Phase 1/Phase 2
Start date December 1, 2021
Completion date June 1, 2022

See also
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