Keytruda (pembrolizumab), manufactured by pharma giant Merck & Co (MYSE: MRK), has achieved an overall response rate of 66% in transplant-ineligible and failure patients with relapsed/refractory classical Hodgkin's lymphoma whose disease progressed on or after brentuximab vedotin treatment.
These early study findings on Merck’s anti-PD-1 therapy were presented at the American Society for Hematology's 56th annual meeting.
Complete remission was achieved in 21% of patients in the study. At the time of analysis, 89% of responses were ongoing with the median duration of response not yet reached.
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