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Merck s 21-Valent Pneumococcal Conjugate Vaccine Gets FDA s Priority Review

The FDA has accepted for Priority Review the BLA for V116, an investigational 21-valent pneumococcal conjugate vaccine for adults.

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FDA approval expands Welireg to patients with renal cell carcinoma

The oral treatment belzutifan, developed by MSD (known as Merck in the US) and branded as Welireg, has received the green light from the US Food and Drug Administration (FDA) for the treatment of an advanced form of renal cell carcinoma (RCC).

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Welireg Approved for Advanced Renal Cell Carcinoma

The FDA has approved Welireg (belzutifan) for the treatment of adult patients with advanced RCC following a PD-1 or PD-L1 inhibitor and a VEGF-TKI.

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Merck (MRK) Announces FDA Approval of WELIREG

Merck (MRK) Announces FDA Approval of WELIREG
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FDA Approves Merck s WELIREG® (belzutifan) for the Treatment of Patients With Advanced Renal Cell Carcinoma (RCC) Following a PD-1 or PD-L1 Inhibitor and a VEGF-TKI

FDA Approves Merck s WELIREG® (belzutifan) for the Treatment of Patients With Advanced Renal Cell Carcinoma (RCC) Following a PD-1 or PD-L1 Inhibitor and a VEGF-TKI
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