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Trial of relatlimab plus nivolumab in pediatric and young adult participants with relapsed or refractory classical Hodgkin's lymphoma and non-Hodgkin's lymphoma.
THE OBJECTIVE OF THIS STUDY IS TO OBTAIN INFORMATION ON THE SAFETY AND EFFICACY OF NIVOLUMAB AND RELATLIMAB IN PARTICIPANTS WITH CLASSICAL HODGKIN'S LYMPHOMA AND RELAPSED/RECURRENT OR REFRACTORY NON-HODGKIN'S LYMPHOMA.
Technical Summary
- PHASE I/II STUDY OF THE SAFETY, TOLERABILITY, PHARMACOKINETICS AND PRELIMINARY EFFICACY OF RELATLIMAB PLUS NIVOLUMAB IN PEDIATRIC AND YOUNG ADULT PARTICIPANTS WITH RELAPSED OR REFRACTORY CLASSICAL HODGKIN'S LYMPHOMA AND NON-HODGKIN'S LYMPHOMA. IMMUNOTHERAPY
- Code EudraCT: 2021-000493-29
- Protocol number: CA224-069
- Promoter: Bristol Myers Squibb
- Molecule/Drug: relatlimab
* 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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