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Benzinga
Benzinga
Business
Vandana Singh

FDA Clears Merck's One-Minute Cancer Shot

Merck FDA Cancer MRK United States
South,San,Francisco,,Ca,,Usa,-,May,1,,2022:,Merck

The U.S. Food and Drug Administration (FDA) on Friday approved Merck & Co. Inc.’s (NYSE:MRK) Keytruda Qlex (pembrolizumab and berahyaluronidase alfa-pmph) injection for subcutaneous administration in adults across most solid tumor indications for Keytruda.

Berahyaluronidase alfa is a variant of human hyaluronidase developed and manufactured by Alteogen Inc.

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