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)
Latest Information Update: 26 Dec 2024
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At a glance
- Drugs Favezelimab/pembrolizumab (Primary) ; Bendamustine; Gemcitabine
- Indications Hodgkin's disease
- Focus Registrational; Therapeutic Use
- Acronyms KEYFORM-008; MK-4280A-008
- Sponsors Merck Sharp & Dohme
- 20 Dec 2024 Status changed from recruiting to active, no longer recruiting.
- 16 Dec 2024 the company has decided to end the favezelimab clinical development program, and will stop enrollment in the Phase 3 KEYFORM-008 trial evaluating the fixed-dose combination of favezelimab and pembrolizumab in patients with relapsed or refractory classical Hodgkin lymphoma.
- 16 Jun 2024 Study design presented at the 29th Congress of the European Haematology Association