martes, 22 de diciembre de 2015

Pembrolizumab label updated with new clinical trial information

FDA (U.S. Food and Drug Administration)
On December 18, 2015, the U. S. Food and Drug Administration (FDA) expanded the label to include the approval of pembrolizumab (Keytruda® Injection, Merck Sharp & Dohme Corp.) for the treatment of patients with unresectable or metastatic melanoma. This expansion now includes the initial treatment of patients with unresectable or metastatic melanoma with pembrolizumab. More information:http://www.fda.gov/Drugs/InformationOnDrugs/ApprovedDrugs/ucm478493.htm

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