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Phase II clinical trial to evaluate the efficacy and safety of Pirtobrutinib in participants with leukemia who have previously received treatment with a covalent Bruton's tyrosine kinase inhibitor.
CLINICAL TRIAL TO COMPARE THE OVERALL RESPONSE RATE OF: - PIRTOBRUTINIB 200 MG VS. 120 MG - PIRTOBRUTINIB 200 MG VS. 60 MG
Specialist
Hematology and Hemotherapy Department
Madrid headquarters
Technical Summary
- PHASE II, OPEN-LABEL, RANDOMIZED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF 3 DOSES OF PYRTOBRUTINIB IN PARTICIPANTS WITH RELAPSED OR REFRACTORY CHRONIC LYMPHOCYTIC LEUKEMIA/SMALL CELL LYMPHOCYTIC LYMPHOMA WHO HAVE PREVIOUSLY RECEIVED TREATMENT WITH A COVALENT BRUTON'S TYROSINE KINASE INHIBITOR.
- Code EudraCT: 2024-515689-15-00
- Protocol number: J2N-MC-JZNX
- Promoter: Lilly
- Molecule/Drug: Pirtobrutinib
- Link to Clinical Trials
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