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BioWorld - Friday, February 13, 2026
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BioWorld, Regulatory
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Regulatory actions for Nov. 11, 2020

Nov. 11, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Angiocrine, Bioxcel, Gyroscope, Inventiva, Sebela, Sorrento, Surface.
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Lilly’s COVID-19 antibody has emergency use authorization; who will receive it?

Nov. 10, 2020
By Lee Landenberger
Now that the FDA has granted emergency use authorization to Eli Lilly and Co.’s bamlanivimab, the company plans to manufacture up to 1 million doses of the therapy by year-end with worldwide distribution to mild to moderate COVID-19 patients ages 12 and older in early 2021.
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Regulatory front

Fed Circuit prolongs inventorship battle

Nov. 10, 2020
By Mari Serebrov
The latest global regulatory news, changes and updates affecting biopharma, including: CDC updates vaccine guidance; Russia launches doctor-driven shortage reporting service; MHRA reviewing acne drug risks.
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Regulatory actions for Nov. 10, 2020

Nov. 10, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Betterlife, Clinigen, Emmaus, Forma, Immune-Onc, Lilly, Oryzon, Praxis, Rafael, Supernus.
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Regulatory actions for Nov. 9, 2020

Nov. 9, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Amo, Astrazeneca, Axovant, Bayer, Beigene, Eusa, Impel, Liminal, Novavax, Orphazyme, Sorrento.
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Regulatory front

FDA: COVID-19 shows why diversity needed in trials

Nov. 9, 2020
By Mari Serebrov
The latest global regulatory news, changes and updates affecting biopharma, including: Final analysis: hydroxychloroquine offers no benefit; FDA finalizes PDUFA VI fee guidance.
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Neurology illustration

Aducan't-umab? Biogen FDA panel for Alzheimer's prospect goes south

Nov. 6, 2020
By Randy Osborne
Talk turned skeptical well before lunchtime in the meeting of the FDA’s Peripheral and Central Nervous System Drugs Advisory Committee to consider Biogen Inc.’s aducanumab for Alzheimer’s disease, and it stayed that way until the end, when panelists voted thumbs down.
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NICE reviews how it evaluates drugs, devices and diagnostics

Nov. 6, 2020
By Nuala Moran
LONDON – After a year in the mill, the U.K. National Institute for Health and Care Excellence (NICE) has put proposals for how it intends to evaluate drugs, devices and diagnostics in the future out for consultation.
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Regulatory actions for Nov. 6, 2020

Nov. 6, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Astrazeneca, Astellas, Basilea, Gosun, Bristol Myers Squibb, Lipocine, Sarepta, Sedor, Senhwa.
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Fed Circuit answers Hatch-Waxman infringement venue question

Nov. 5, 2020
By Mari Serebrov
The U.S. Court of Appeals for the Federal Circuit narrowed the landscape for filing Hatch-Waxman infringement suits against U.S.-based companies, as it answered yet another question raised by the Supreme Court’s unanimous decision in TC Heartland v. Kraft Foods, which dramatically changed venue parameters in 2017 for all patent infringement cases.
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