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Trial of mosunetuzumab or glofitamab in combination with cc-220 and cc-99282 in patients with b-lymphocyte non-Hodgkin's lymphoma
THE PURPOSE OF THIS STUDY IS TO ANALYZE THE SAFETY AND EFFICACY OF MOSUNETUZUMAB IN COMBINATION WITH CC-220 OR CC-99282 (GROUP 1), OR GLOFITAMAB AND OBINUTUZUMAB IN COMBINATION WITH CC-220 OR CC-99282 (GROUP 2) AT DIFFERENT DOSE LEVELS AND DOSING SCHEDULES TO FIND OUT WHAT EFFECTS THIS DRUG COMBINATION HAS, EITHER GOOD OR BAD, ON YOU AND YOUR CANCER.
Technical Summary
- PHASE IB, OPEN-LABEL, MULTICENTER STUDY TO EVALUATE THE SAFETY, PHARMACOKINETICS AND EFFICACY OF MOSUNETUZUMAB OR GLOFITAMAB IN COMBINATION WITH CC-220 AND CC-99282 IN PATIENTS WITH B-LYMPHOCYTE NON-HODGKIN'S LYMPHOMA
- Code EudraCT: 2021-005745-33
- Protocol number: CO43805
- Promoter: Roche Farma, S.A.
* The trials only admit a limited number of patients and are subject to inclusion and exclusion criteria. The specialist who assesses your case will inform you of the conditions required to participate in the clinical trial.
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Information offered by the Spanish Registry of Clinical Studies
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