FDA approves pembrolizumab for high-risk early-stage triple-negative breast cancer

Food and Drug Administration approved pembrolizumab (Keytruda, Merck) for high-risk, early-stage, triple-negative breast cancer (TNBC) in combination with chemotherapy as neoadjuvant treatment, and then continued as a single agent as adjuvant treatment after surgery. July 26, 2021. More Information: https://www.fda.gov/drugs/drug-approvals-and-databases/fda-approves-pembrolizumab-high-risk-early-stage-triple-negative-breast-cancer Manage Subscriptions  |  Unsubscribe All  |  Help This email was sent to ooseims.archieves@blogger.com using GovDelivery Communications Cloud on behalf of: U.S. Food and Drug Administration ·  10903 New Hampshire Ave · Silver Spring, MD ·  20993-0002 ·  1-888-INFO-FDA