Industry News Archive

FDA Approves Expanded Indication of Pembrolizumab for R/R cHL

On October 15, 2020, the U.S. Food and Drug Administration (FDA) approved an expanded label for Keytruda® (pembrolizumab) as a monotherapy for the treatment of adult patients with relapsed or refractory (R/R) classical Hodgkin lymphoma (cHL). Keytruda is the first anti-PD-1 therapy approved for adult patients with relapsed or refractory cHL after frontline therapy.

Read Merck's press release and the FDA announcement.

Posted 10/15/2020

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