Keytruda keeps expanding with another priority review; Medicxi-backed eye drop maker wins new funding, regional deal
As Merck continues to chop away at a path to earlier lines of cancer treatment for Keytruda, the FDA is offering a hand.
The agency has granted priority review for the PD-1 star as an adjuvant therapy in certain patients with renal cell carcinoma — which, if approved, would mark the latest in a streak of label expansions.
Specifically, it would be targeting patients who have intermediate-high or high risk of recurrence even after surgical removal of a kidney, or following nephrectomy and resection of metastatic lesions.
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