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Phase I/II FIH trial of REGN5458 in patients with relapsed or refractory multiple myeloma.
THE MAIN PURPOSE OF THIS STUDY IS TO OBTAIN MORE INFORMATION ON THE SAFETY OF REGN5458 AND TO FIND THE MOST APPROPRIATE DOSE OF REGN5458 FOR THE TREATMENT OF PATIENTS WITH MULTIPLE MYELOMA.
Technical Summary
- PHASE I/II FIH STUDY OF REGN5458 (ANTI-BCMA X BISPECIFIC ANTI-CD3 ANTIBODY) IN PATIENTS WITH RELAPSED OR REFRACTORY MULTIPLE MYELOMA
- Code EudraCT: 2018-003188-78
- Protocol number: R5458-ONC-1826
- Promoter: Regeneron Pharmaceuticals, Inc.
* 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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