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Biogen (BIIB) Shares Down 4% As Head of FDA Calls for a Federal Investigation into Approval of Aduhelm
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Collaboration Between AbbVie, Biogen and Pfizer Creates World’s Largest Browsable Resource Linking Rare Protein-Coding Genetic Variants to Human Health and Disease
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Collaboration Between AbbVie, Biogen and Pfizer Creates World’s Largest Browsable Resource Linking Rare Protein-Coding Genetic Variants to Human Health and Disease
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Biogen (BIIB) Announces FDA Approves Updated ADUHELM Prescribing Information to Emphasize Population Studied in Clinical Trials
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FDA Approves Updated ADUHELM™ Prescribing Information to Emphasize Population Studied in Clinical Trials
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FDA Approves Updated ADUHELM™ Prescribing Information to Emphasize Population Studied in Clinical Trials
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Samsung Bioepis and Biogen (BIIB) Receive Positive CHMP Opinion for Ranibizumab Biosimilar, BYOOVIZ
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Samsung Bioepis and Biogen Receive Positive CHMP Opinion for Ranibizumab Biosimilar, BYOOVIZ™
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Samsung Bioepis and Biogen Receive Positive CHMP Opinion for Ranibizumab Biosimilar, BYOOVIZ™
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Eisai, Biogen (BIIB) Announce U.S. FDA Grants Breakthrough Therapy Designation For Lecanemab (BAN2401), An Anti-Amyloid Beta Protofibril Antibody For The Treatment Of Alzheimer's Disease
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Eisai And Biogen Inc. Announce U.S. FDA Grants Breakthrough Therapy Designation For Lecanemab (BAN2401), An Anti-Amyloid Beta Protofibril Antibody For The Treatment Of Alzheimer's Disease
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Biogen (BIIB) Announces First Patient Dosed in Phase 3 Systemic Lupus Erythematosus Study
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Biogen Announces First Patient Dosed in Phase 3 Systemic Lupus Erythematosus Study
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Biogen Announces First Patient Dosed in Phase 3 Systemic Lupus Erythematosus Study
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Biogen (BIIB) Announces Topline Results From Phase 2 Study of Gosuranemab, an Anti-Tau Antibody, for Alzheimer’s Disease
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Biogen Announces Topline Results From Phase 2 Study of Gosuranemab, an Anti-Tau Antibody, for Alzheimer’s Disease
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Biogen Announces Topline Results From Phase 2 Study of Gosuranemab, an Anti-Tau Antibody, for Alzheimer’s Disease
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Sage Therapeutics (SAGE), Biogen (BIIB) Phase 3 for Zuranolone for Major Depressive Disorder Shows Statistically Significant Improvement
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Sage Therapeutics and Biogen Announce Positive Pivotal Phase 3 Results for Zuranolone, an Investigational Two-Week, Once-Daily Therapeutic Being Evaluated for Major Depressive Disorder
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Sage Therapeutics and Biogen Announce Positive Pivotal Phase 3 Results for Zuranolone, an Investigational Two-Week, Once-Daily Therapeutic Being Evaluated for Major Depressive Disorder
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Sage Therapeutics and Biogen Announce Positive Pivotal Phase 3 Results for Zuranolone, an Investigational Two-Week, Once-Daily Therapeutic Being Evaluated for Major Depressive Disorder
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Biogen (BIIB) Phase 3 Gene Therapy Study in Choroideremia Did Not Meet its Primary Endpoint
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Biogen Announces Topline Results from Phase 3 Gene Therapy Study in Choroideremia
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Biogen Announces Topline Results from Phase 3 Gene Therapy Study in Choroideremia
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Biogen Announces Investor Day on September 21, 2021
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Biogen Announces Investor Day on September 21, 2021
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Biogen (BIIB) Says New Data at Cure SMA 2021 Highlight Long-Term Efficacy of SPINRAZA and its Commitment to Innovation in SMA Therapy
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New Data at Cure SMA 2021 Highlight the Long-Term Efficacy of SPINRAZA® (nusinersen) and Biogen’s Commitment to Innovation in SMA Therapy
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New Data at Cure SMA 2021 Highlight the Long-Term Efficacy of SPINRAZA® (nusinersen) and Biogen’s Commitment to Innovation in SMA Therapy
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Biogen (BIIB) Confirms FDA Accelerated Approval for Alzheimer's Treatment ADUHELM
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Biogen and Eisai launch multiple initiatives to help patients with Alzheimer’s disease access ADUHELM™
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Biogen and Eisai launch multiple initiatives to help patients with Alzheimer’s disease access ADUHELM™
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FDA grants accelerated approval for ADUHELM™ as the first and only Alzheimer’s disease treatment to address a defining pathology of the disease
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FDA grants accelerated approval for ADUHELM™ as the first and only Alzheimer’s disease treatment to address a defining pathology of the disease
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Biogen (BIIB), Bio-Thera Announce Positive Results From Phase 3 Study of BAT1806, a Proposed Biosimilar Referencing Actemra
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Biogen and Bio-Thera Announce Positive Results From Phase 3 Study of BAT1806, a Proposed Biosimilar Referencing Actemra® (Tocilizumab)
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Biogen and Bio-Thera Announce Positive Results From Phase 3 Study of BAT1806, a Proposed Biosimilar Referencing Actemra® (Tocilizumab)
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Biogen (BIIB), Ginkgo Bioworks Announce Collaboration and License Agreement to Develop Novel Gene Therapy Manufacturing Platform
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Biogen and Ginkgo Bioworks Announce Collaboration and License Agreement to Develop Novel Gene Therapy Manufacturing Platform
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Biogen and Ginkgo Bioworks Announce Collaboration and License Agreement to Develop Novel Gene Therapy Manufacturing Platform
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Swissmedic Grants Good Manufacturing Practice Multi-Product License to Biogen Biologics Facility in Solothurn, Switzerland
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Swissmedic Grants Good Manufacturing Practice Multi-Product License to Biogen Biologics Facility in Solothurn, Switzerland
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Biogen (BIIB) Announces Topline Results From Phase 2/3 Gene Therapy Study for XLRP
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Biogen Announces Topline Results From Phase 2/3 Gene Therapy Study for XLRP
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Biogen Announces Topline Results From Phase 2/3 Gene Therapy Study for XLRP
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Biogen and Envisagenics Announce Collaboration to Advance RNA Splicing Research
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Biogen and Envisagenics Announce Collaboration to Advance RNA Splicing Research
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Biogen (BIIB) Announces Exercise of Option to Acquire the Investigational Drug TMS-007 for Acute Ischemic Stroke Based on Positive Phase 2a Data
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Biogen Announces Exercise of Option to Acquire the Investigational Drug TMS-007 for Acute Ischemic Stroke Based on Positive Phase 2a Data
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Biogen Announces Exercise of Option to Acquire the Investigational Drug TMS-007 for Acute Ischemic Stroke Based on Positive Phase 2a Data

