BRIEF-FDA Approves Merck’S WELIREG® (Belzutifan) For The Treatment Of Adults And Pediatric Patients 12 Years And Older With Locally Advanced, Unresectable, Or Metastatic Pheochromocytoma Or Paraganglioma (PPGL)

Reuters

15 May

BRIEF-FDA Approves Merck’S WELIREG® (Belzutifan) For The Treatment Of Adults And Pediatric Patients 12 Years And Older With Locally Advanced, Unresectable, Or Metastatic Pheochromocytoma Or Paraganglioma (PPGL)

May 14 (Reuters) - Merck & Co Inc MRK.N:

FDA APPROVES MERCK’S WELIREG® (BELZUTIFAN) FOR THE TREATMENT OF ADULTS AND PEDIATRIC PATIENTS 12 YEARS AND OLDER WITH LOCALLY ADVANCED, UNRESECTABLE, OR METASTATIC PHEOCHROMOCYTOMA OR PARAGANGLIOMA (PPGL)
MERCK & CO INC: WELIREG LABEL CONTAINS A BOXED WARNING THAT EXPOSURE TO WELIREG DURING PREGNANCY CAN CAUSE EMBRYO-FETAL HARM

Source text: ID:nBw28TVK8a

Further company coverage: MRK.N

((Reuters.Briefs@thomsonreuters.com;))

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