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Merck Announces Expiration of Hart-Scott-Rodino Act Waiting Period and Extension of Tender Offer to Acquire Acceleron Pharma Inc.
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Merck (MRK) Acquisition of Acceleron Pharma Cleared by Antitrust Authorities in Germany and Austria
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Merck Announces Receipt of Antitrust Clearance in Germany and Austria Relating to Tender Offer to Acquire Acceleron Pharma Inc.
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Merck Announces Withdrawal and Refiling under the Hart-Scott-Rodino Act and Extension of Tender Offer to Acquire Acceleron Pharma Inc.
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UPDATE: Merck (MRK) Commences Cash Tender Offer to Acquire Acceleron Pharma (XLRN) for $180/sh, Deal Announced on Sept. 30
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Merck Begins Tender Offer to Acquire Acceleron Pharma Inc.
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Merck (MRK) to Acquire Acceleron Pharma (XLRN) for $180 Per Share in $11.5 Billion Deal
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Merck to Acquire Acceleron Pharma Inc.
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Bristol Myers Squibb Reports Second Quarter Financial Results for 2021
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Bristol-Myers Squibb (BMY), Acceleron (XLRN) Present First Results from Phase 2 BEYOND Study of Reblozyl in Adults with NTD Beta Thalassemia
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Bristol Myers Squibb and Acceleron Present First Results from Phase 2 BEYOND Study of Reblozyl® (luspatercept-aamt) in Adults with Non-Transfusion Dependent (NTD) Beta Thalassemia
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Bristol Myers Squibb Canada (BMY), Acceleron Pharma (XLRN) Announce Health Canada Approves REBLOZYL, New Class of Treatment for Adult Patients Living With Myelodysplastic Syndromes
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Health Canada Approves REBLOZYL® (luspatercept), New Class of Treatment for Adult Patients Living With Myelodysplastic Syndromes
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Health Canada Approves REBLOZYL® (luspatercept), New Class of Treatment for Adult Patients Living with Beta Thalassemia
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Bristol-Myers Squibb (BMY) Announces EMA Approves Reblozyl for Treatment of Transfusion-Dependent Anemia in Adult Patients with Myelodysplastic Syndromes or Beta Thalassemia
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European Commission Approves Reblozyl (luspatercept) for the Treatment of Transfusion-Dependent Anemia in Adult Patients with Myelodysplastic Syndromes or Beta Thalassemia
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Bristol (BMY) and Acceleron (XLRN) Announce Reblozyl Receives Positive CHMP Opinion for Treatment of Adults with Anemia in Beta Thalassemia and Myelodysplastic Syndromes
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Reblozyl (luspatercept) Receives Positive CHMP Opinion for the Treatment of Adults with Anemia in Beta Thalassemia and Myelodysplastic Syndromes
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U.S. Food and Drug Administration (FDA) Approves Reblozyl® (luspatercept-aamt), the First and Only Erythroid Maturation Agent, to Treat Anemia in Adults with Lower-Risk Myelodysplastic Syndromes (MDS
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Bristol-Myers Squibb (BMY) and Acceleron (XLRN) Announces NEJM Publishes Results from Pivotal Phase 3 BELIEVE Trial of Reblozyl in Adult Patients With Beta Thalassemia
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New England Journal of Medicine Publishes Results from Pivotal Phase 3 BELIEVE Trial of Reblozyl (luspatercept-aamt) in Adult Patients With Beta Thalassemia
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Bristol-Myers Squibb (BMY), Acceleron (XLRN) Announce NEJM Publishes Results of Pivotal Phase 3 Reblozyl MEDALIST Trial
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New England Journal of Medicine Publishes Results of Pivotal Phase 3 Reblozyl® (luspatercept-aamt) MEDALIST Trial
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Bristol-Myers Squibb (BMY), Acceleron (XLRN) Announce Reblozyl Studies Evaluating Treatment of Anemia in Rare Blood Diseases Presented at ASH
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Reblozyl® (luspatercept-aamt) Studies Evaluating Treatment of Anemia in Rare Blood Diseases Presented at American Society of Hematology (ASH) Annual Meeting
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Bristol-Myers Squibb (BMY), Acceleron Pharma (XLRN) Announces FDA Will Not Review Reblozyl at ODAC Meeting
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Bristol-Myers Squibb and Acceleron Pharma Provide Update on FDA Advisory Committee for Reblozyl® (luspatercept-aamt)
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Bristol-Myers Squibb (BMY), Acceleron Pharma (XLRN) Announce FDA Advisory Committee Will Review Reblozyl for Use in Patients With Myelodysplastic Syndromes
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Bristol-Myers Squibb and Acceleron Pharma Announce FDA Advisory Committee Will Review Reblozyl® (luspatercept-aamt) for Use in Patients With Myelodysplastic Syndromes
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FDA Approves REBLOZYL® (luspatercept-aamt) for the Treatment of Anemia in Adults With Beta Thalassemia Who Require Regular Red Blood Cell Transfusions
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Celgene (CELG), Acceleron Pharma (XLRN) Announce FDA Accepts Luspatercept BLA in Myelodysplastic Syndromes and Beta-Thalassemia
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Celgene Corporation and Acceleron Pharma Announce U.S. FDA Accepts Luspatercept Biologics License Application in Myelodysplastic Syndromes and Beta-Thalassemia
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Celgene Corporation and Acceleron Pharma Announce Submission of Luspatercept Marketing Authorization Application to the European Medicines Agency (EMA) for MDS and Beta-Thalassemia
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Celgene (CELG), Acceleron Pharma (XLRN) Announce Submission of Luspatercept BLA to U.S. FDA
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Celgene Corporation and Acceleron Pharma Announce Submission of Luspatercept Biologics License Application to U.S. FDA
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Celgene (CELG), Acceleron Pharma (XLRN) Report Results of the Phase 3 MEDALIST Trial Evaluating Luspatercept in Patients with Myelodysplastic Syndromes
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Celgene Corporation and Acceleron Pharma Announce Results of the Phase 3 MEDALIST Trial Evaluating Luspatercept in Patients with Myelodysplastic Syndromes at the ASH 2018 Plenary Session
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Celgene Corporation and Acceleron Pharma Announce Results of the Phase 3 BELIEVE Trial Evaluating Luspatercept in Adult Patients with Beta-Thalassemia at ASH 2018
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Leading Protein Scientist Dr. Asya Grinberg Joins Dragonfly Therapeutics as Head of Biologics
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Celgene (CELG), Acceleron (XLRN) Announces Preliminary Results from Two Phase 2 Trials of Luspatercept in Beta-Thalassemia Presented at ASH
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Celgene and Acceleron Announce New Results from an Investigational Study with Luspatercept in Beta-Thalassemia Presented at the 57th American Society of Hematology (ASH) Annual Meeting and Exposition
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Celgene and Acceleron Announce New Results from an Investigational Study with Luspatercept in Myelodysplastic Syndromes Presented at the 57th American Society of Hematology (ASH) Annual Meeting and Ex
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Bayer CropScience and Flagship Ventures Form Strategic Innovation Partnership to Fund Leading-Edge Agriculture Ventures

