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A Phase 3 Randomized Clinical Study of MK-4280A Coformulated Favezelimab MK-4280 plus Pembrolizumab MK-3475 Versus Physician's Choice Chemotherapy in PD-(L)1-Refractory, Relapsed or Refractory Classical Hodgkin Lymphoma (KEYFORM-008).

Primary Objective:
To compare MK-4280A to physicians choice chemotherapy with respect to PFS per Lugano response criteria by BICR

Secondary Objectives:
- To compare MK-4280A to physicians choice chemotherapy with respect to OS

- To evaluate MK-4280A and physicians choice chemotherapy with respect to
ORR per Lugano response criteria by BICR

- To evaluate MK-4280A and physicians choice chemotherapy with respect to DOR per Lugano response criteria by BICR

- To evaluate the safety and tolerability of MK-4280A

Protocol Number: 012315
Phase: Phase III
Applicable Disease Sites: Hodgkin's Lymphoma
Drugs Involved: BENDAMUSTINE
Favezelimab (MK4280A)
GEMCITABINE
Principal Investigator: Matthew Matasar
Scope: National
Therapies Involved: Chemotherapy single agent systemic
Participating Institutions:
  • RWJBarnabas Health
    • Community Medical Center
    • Jersey City Medical Center, Jersey City
    • Monmouth Medical Center
  • Rutgers University
Inclusion & Exclusion Criteria

Please note that we have obtained the inclusion and exclusion criteria information from the National Institutes of Health’s clinical trials web site ClinicalTrials.gov. The listed criteria may not necessarily reflect recent amendments to the protocol and the current criteria.

For further information about clinical trials, please contact us at 732-235-7356.