
FDA Approves Pembrolizumab (KEYTRUDA®) for Classical Hodgkin Lymphoma
New York, NY (March 14, 2017) – The U.S. Food and Drug Administration (FDA) announced it has approved the use of pembrolizumab (KEYTRUDA ®) to treat patients with refractory classical Hodgkin lymphoma (cHL), or those who have relapsed after three…