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Clinical Trial Summary

This is a single arm, multi-center study to evaluate the efficacy and safety of orelabrutinib for Chronic lymphocytic lymphoma(CLL)/small lymphocytic lymphoma (SLL) patients who are slowly responding to Ibrutinib switched to Orelabrutinib.


Clinical Trial Description

The eligible CLL/SLL patients who are slowly responding to Ibrutinib will be switched to Orelabrutinib treatment. The patients will receive Orelabrutinib 150mg oral daily (28 days/cycle) for up to 2 year or until disease progression, intolerable toxicity, death, informed consent withdrawal or lost of follow up (whichever occurs first). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05491044
Study type Interventional
Source Peking University People's Hospital
Contact Shenmiao Yang
Phone +8601088326666
Email yangshenmiao@hotmail.com
Status Recruiting
Phase Phase 2
Start date January 1, 2022
Completion date August 30, 2024

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