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UnknownNCT05124028

A Study of Orelabrutinib in Patients With ITP

A Study of Orelabrutinib in Patients With Primary Immune Thrombocytopenia (ITP)

Status
Unknown
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
10 (estimated)
Sponsor
Peking University People's Hospital · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

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).

Detailed 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.

Conditions

Interventions

TypeNameDescription
DRUGOrelabrutinib50mg po qd 6 weeks

Timeline

Start date
2021-12-01
Primary completion
2022-03-01
Completion
2022-06-01
First posted
2021-11-17
Last updated
2021-11-17

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05124028. Inclusion in this directory is not an endorsement.