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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.

Imagen de la Dra. Paula Rodríguez Otero, especialista enHematología de la Clínica Universidad de Navarra. La Dra. Rodríguez se dedica preferencialmente al estudio y tratamiento del mieloma múltiple y el trasplante alogénico.
Dr. Paula Rodríguez Otero Curriculum
Specialist Hematology and Hemotherapy Department
Navarre headquarters
Madrid headquarters
Cancer Center
Hematologic Cancer Area
Status
In recruitment
headquarters
Pamplona

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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Information offered by the Spanish Registry of Clinical Studies

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