Merck (NYSE:MRK) received FDA approval for KEYTRUDA and subcutaneous KEYTRUDA QLEX for platinum resistant ovarian cancer, including a companion diagnostic. The approvals represent the first PD 1 ...
Source LinkMerck (NYSE:MRK) received FDA approval for KEYTRUDA and subcutaneous KEYTRUDA QLEX for platinum resistant ovarian cancer, including a companion diagnostic. The approvals represent the first PD 1 ...
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