Biogen Inc.

Location

Massachusetts

Founded

1978-02-28

Risk Signals

6609 news mentions monitored

Industry Context

This company is tracked across risk categories, including those related to its sector (e.g., Pharmaceutical Preparations, Biological Products, Except Diagnostic Substances, Commercial Physical and Biological Research), including supply chain integrity, ESG practices, labor disputes, and regulatory compliance.

Recent Articles about Biogen Inc.

Live alerts from global media, monitored by Business Radar

Positive Phase III Results for Genentech’s Gazyva Show Superiority to Standard Therapy Alone in People With Lupus Nephritis

2024-09-26 (biospace.com)

Positive Phase III Results for Genentech’s Gazyva Show Superiority to Standard Therapy Alone in People With Lupus Nephritis

– The REGENCY study met its primary endpoint, demonstrating statistically significant and clinically meaningful treatment benefits in people with active lupus nephritis –

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Nishtha Jain: Bridging Technology and Healthcare for Better Patient Care

2024-07-22 (ciolook.com)

Nishtha Jain: Bridging Technology and Healthcare for Better Patient Care

Innovating Healthcare Solutions!

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An explainable machine learning-based phenomapping strategy for adaptive predictive enrichment in randomized clinical trials - npj Digital Medicine

2023-11-25 (nature.com)

An explainable machine learning-based phenomapping strategy for adaptive predictive enrichment in randomized clinical trials - npj Digital Medicine

Randomized clinical trials (RCT) represent the cornerstone of evidence-based medicine but are resource-intensive. We propose and evaluate a machine learning (ML) strategy of adaptive predictive enrichment through computational trial phenomaps to optimize RCT enrollment. In simulated group sequential

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FDA Approves ZURZUVAETM (zuranolone), the First and Only Oral Treatment Approved for Women with Postp

2023-08-05 (pharmiweb.com)

FDA Approves ZURZUVAETM (zuranolone), the First and Only Oral Treatment Approved for Women with Postp

Postpartum depression (PPD) approval based on results from two Phase 3 clinical trials; in the SKYLARK Study treatment with ZURZUVAE rapidly improved symptoms of PPD at Day 15 and as early as Day 3 with sustained effect to Day 45Mental health conditions are the leading cause of maternal mortality...

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FDA Approves ZURZUVAETM (zuranolone), the First and Only Oral Treatment Approved for Women with Postpartum Depression, and Issues a Complete Response Letter for Major Depressive Disorder

2023-08-05 (globenewswire.com)

FDA Approves ZURZUVAETM (zuranolone), the First and Only Oral Treatment Approved for Women with Postpartum Depression, and Issues a Complete Response Letter for Major Depressive Disorder

Postpartum depression (PPD) approval based on results from two Phase 3 clinical trials; in the SKYLARK Study treatment with ZURZUVAE rapidly improved...

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#AAN2022 - In SMA Children, Spinraza Showing Safety After Zolgensma

2022-04-29 (smanewstoday.com)

#AAN2022 - In SMA Children, Spinraza Showing Safety After Zolgensma

Early safety findings were good in 9 children, all with a suboptimal response to Zolgensma, being treated with Spinraza in the RESPOND trial.

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Health Care Down After Earnings - Health Care Roundup

2017-10-24 (foxbusiness.com)

Health Care Down After Earnings - Health Care Roundup

Shares of health-care companies fell amid mixed earnings reports. Shares of Biogen slid after analysts noted that U.S. quarterly sales of its Spinraza therapy for spinal muscular atrophy were flat from a year earlier. Alexion ticked up after the Food and Drug Administration approved a wider

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UK launch for Biogen’s biosimilar infliximab

2016-09-07 (pharmatimes.com)

UK launch for Biogen’s biosimilar infliximab

Biogen has launched Flixabi - a biosimilar of Johnson & Johnson's blockbuster infliximab - across the UK for use in a range of chronic inflammatory conditions.

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Health News Roundup: Cough syrup deaths overseas prompt US crackdown on toxic testing; Japan approves Alzheimer's treatment Leqembi by Eisai and Biogen and more

(devdiscourse.com)

Health News Roundup: Cough syrup deaths overseas prompt US crackdown on toxic testing; Japan approves Alzheimer's treatment Leqembi by Eisai and Biogen and more

The Food and Drug Administration has reprimanded at least 28 companies this year, saying they failed to prove sufficient testing of ingredients used in over-the-counter drugs and consumer products for the toxins ethylene glycol( EG) and diethylene glycol( DEG), according to a Reuters analysis of

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