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Merck to Acquire Acceleron Pharma Inc.

Merck (NYSE: MRK), known as MSD outside the United States and Canada, and Acceleron Pharma Inc. (Nasdaq: XLRN), a publicly traded biopharmaceutical company, today announced that the companies have entered into a definitive agreement under which Merck, through a subsidiary, will acquire Acceleron for $180 per share ...
United States United Kingdom Rob Davis Jp Morgan Securities Credit Suisse Securities United States Ropes Gray

Leslie A. Brun Resigns from Merck Board of Directors

Merck known as MSD outside the United States and Canada, announced today that Leslie A. Brun, its independent lead director, has resigned from its Board of Directors, effective August 19, 2021. Mr. Brun is stepping down due to his decision to become chairman and chief executive officer of Ariel Alternatives, LLC, a subsidiary of Ariel Investments, LLC, a private equity initiative being created to help scale ...
United States Lesliea Brun Rob Davis Facebook Instagram Youtube Patrick Ryan Peter Dannenbaum

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FDA Approves Merck's Hypoxia-Inducible Factor-2 Alpha Inhibitor WELIREG for the Treatment of Patients With Certain Types of Von Hippel-Lindau Disease-Associated Tumors

WELIREG Approved for Adult Patients With VHL Disease Who Require Therapy for Associated Renal Cell Carcinoma, Central Nervous System Hemangioblastomas, or Pancreatic Neuroendocrine Tumors, Not Requiring Immediate Surgery WELIREG Expands Merckโ€™s Oncology Portfolio as the First and Only Systemic Therapy Approved for These Patients With VHL Disease Merck known as MSD outside the United States and Canada, today ...
United States Scot Ebbinghaus Ramaprasad Srinivasan Peter Dannenbaum Eric Jonasch Melissa Moody

FDA Approves KEYTRUDA® Plus LENVIMA® Combination for First-Line Treatment of Adult Patients With Advanced Renal Cell Carcinoma

KEYTRUDA Plus LENVIMA Is Now Approved for Two Types of Cancer, Including Advanced RCC Based on Phase 3 CLEARKEYNOTE-581 Trial, KEYTRUDA Plus LENVIMA Significantly Reduced Risk of Disease Progression or Death by 61% Versus Sunitinib Merck known as MSD outside the United States and Canada, and Eisai today announced that the U.S. Food and Drug Administration has approved the combination of KEYTRUDA, Merckโ€™s anti-PD-1 ...
United States New Zealand Gregory Lubiniecki Nikki Sullivan Dorothy Byrne Peter Dannenbaum

Merck Announces U.S. FDA Approval of VAXNEUVANCE for the Prevention of Invasive Pneumococcal Disease in Adults 18 Years and Older Caused by 15 Serotypes

Clinical Data Supporting Approval Demonstrated Non-Inferior Immune Responses for the Serotypes Shared with PCV13 VAXNEUVANCE Elicited Superior Immune Responses for Serotypes 3, 22F and 33F Compared to PCV13, Which Are Major Causes of Disease known as MSD outside the United States and Canada, today announced the U.S. Food and Drug Administration approved VAXNEUVANCE โ„ข for active immunization for the prevention of โ€ฆ Clinical Data Supporting Approval Demonstrated Non-Inferior Immune Responses...
United States Peter Dannenbaum Steve Wanczyk Melissa Moody Roy Baynes Jose Cardona

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