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Baricitinib for Steroid-resistant/Relapse Immune Thrombocytopenia — BAITP  

Immune Thrombocytopenia Clinical Trial

Official title:
Efficacy and Safety of Baricitinib for Steroid-resistant/Relapse Immune Thrombocytopenia: A Single-arm, Open-label Phase II Study

Clinical Trial Summary

Single-arm, open-label, single-center study to evaluate the efficacy and safety of baricitinib for the treatment of adults with steroid-resistant/relapse immune thrombocytopenia (ITP).

Clinical Trial Description

The investigators are undertaking a prospective trial of 20 adults with ITP in China. Baricitinib is administered as 4 mg po. daily. Safety outcomes and efficacy outcomes are assessed on scheduled study visits (primary endpoint defined as durable response at 6-month follow-up). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05446831
Study type Interventional
Source Peking University People's Hospital
Contact Xiaohui Zhang, MD
Phone +8613522338836
Email zhangxh100@sina.com
Status Recruiting
Phase Phase 2
Start date July 13, 2022
Completion date December 1, 2023
View Details
See also
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