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Clinical Trial Summary

This study evaluates the effectiveness of acalabrutinib treatment in patients with chronic lymphocytic leukemia (CLL) deemed at high risk for Richter's Transformation (RT). This is a single arm study. Enrolled patients will initiate therapy with acalabrutinib and will dose continuously. While on study, subjects will be monitored monthly for the first 3 months, then every three months thereafter until disease progression, discontinuation due to toxicity, death, or study completion.


Clinical Trial Description

This is a multi-center, single arm, Phase II clinical trial to investigate the effectiveness of acalabrutinib treatment within 6 months of chronic lymphocytic leukemia (CLL) diagnosis for patients with CLL deemed at high risk for Richter's Transformation (RT). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04660045
Study type Interventional
Source Weill Medical College of Cornell University
Contact
Status Withdrawn
Phase Phase 2
Start date May 2022
Completion date June 2026

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