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Phase III, open-label, randomized clinical trial to compare the efficacy and safety of Odronextamab (REGN1979) combined with chemotherapy vs. Rituximab combined with chemotherapy in participants c

THE PRIMARY OBJECTIVE OF THIS STUDY IS TO EVALUATE THE SAFETY, TOLERABILITY AND DOSE-LIMITING TOXICITIES (DLTS) OF ODRONEXTAMAB IN COMBINATION WITH CHEMOTHERAPY IN PARTICIPANTS WITH PREVIOUSLY UNTREATED FL.

Imagen del Dr. Carlos Grande García, especialista en Hematología y Hemoterapia de la Clínica Universidad de Navarra.
Dr. Carlos García Grande Curriculum
Specialist Hematology and Hemotherapy Department
Madrid headquarters
Cancer Center
Hematologic Cancer Area
Status
In recruitment
headquarters
Pamplona/Madrid

Technical Summary

  • PHASE III, OPEN-LABEL, RANDOMIZED STUDY TO COMPARE THE EFFICACY AND SAFETY OF ODRONEXTAMAB (REGN1979), A BISPECIFIC ANTI-CD20 AND ANTI-CD3 ANTIBODY, IN COMBINATION WITH CHEMOTHERAPY VERSUS RITUXIMAB IN COMBINATION WITH CHEMOTHERAPY IN PARTICIPANTS WITH PREVIOUSLY UNTREATED FOLLICULAR LYMPHOMA (OLYMPIA-2).
  • Code EudraCT: 2022-502113-28-00
  • Protocol number: R1979-ONC-2075
  • Promoter: Regeneron Pharmaceuticals, Inc.
  • Molecule/Drug: Odronextamab

* 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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