Conditions
Hodgkin Lymphoma
The purpose of this study is to compare efficacy of coformulated favezelimab/pembrolizumab (MK-4280A) with physician’s choice chemotherapy of bendamustine or gemcitabine in participants with PD-(L)1-refractory, relapsed or refractory classical Hodgkin Lymphoma. The study will also assess the safety and tolerability of coformulated favezelimab/pembrolizumab. The primary study hypotheses are that coformulated favezelimab/pembrolizumab is superior to physician’s choice chemotherapy with respect to progression-free survival (PFS) and overall survival (OS).
CLINICALTRIALS.GOV IDENTIFIER
NCT05508867
EudraCT Number
2022-000371-39
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Conditions
Hodgkin Lymphoma
Age Range
18+
Sex
All
All patients who enroll in the trial will receive study medication while on the study.
50% will receive MK-4280A coformulation of favelizumab and pembrolizumab
50% will receive chemotherapy
In Phase 3 trials, researchers try to find out if a treatment works in a large number of people, usually about 1,000 to 5,000 participants who have the health condition the treatment is intended to treat. In vaccine trials, the participants may be healthy or have diseases or conditions. Phase 3 trials may happen in a doctor’s office, a clinic, or a hospital.
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