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BioWorld - Saturday, July 4, 2026
Breaking News: Science fiction realized: BCI tech is hereBreaking News: Science fiction realized: BCI tech is here
Home » Topics » BioWorld, Regulatory

BioWorld, Regulatory
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Regulatory actions for Feb. 12, 2021

Feb. 12, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Curevac, Immunitybio, Lysogene, Nantkwest, Regeneron, Seagen, Xeris.
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Evkeeza nod expands Regeneron’s cardiovascular franchise

Feb. 11, 2021
By Jennifer Boggs
Regeneron Pharmaceuticals Inc.’s angiopoietin-like 3 (ANGPTL3)-targeting antibody, Evkeeza (evinacumab), won FDA approval for use in reducing LDL cholesterol in patients with homozygous familial hypercholesterolemia.
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Glass vial production line

GAO: Manufacturing the big challenge for COVID-19 vaccines

Feb. 11, 2021
By Mari Serebrov
Limited manufacturing capacity, supply chain disruptions and a dearth of personnel with specialized skills are all challenges vaccine makers are facing as they race to produce contracted quotas of COVID-19 vaccines that were developed and authorized in record time.
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COVID-19 vaccines should be tested against variants, EMA says

Feb. 11, 2021
By Nuala Moran
LONDON – The EMA has requested all COVID-19 vaccine developers to investigate if their products offer protection against new variants of SARS-CoV-2 and to submit the relevant data.
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Regulatory front

NIH, trade groups: More inclusive vaccine research urgently needed

Feb. 11, 2021
By Mari Serebrov
The latest global regulatory news, changes and updates affecting biopharma, including: Fed Circuit agrees Amgen patents lack enablement; HC nudging along with regulatory modernization plan; EMA: No Sputnik application yet.
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Regulatory actions for Feb. 11, 2021

Feb. 11, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Clinuvel, Genmab, Moderna, Oryzon, Polaryx, Seagen.
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EC’s Aspen decision provides guidance on excessive prices

Feb. 10, 2021
By Mari Serebrov
In its first decision on excessive drug pricing, the European Commission (EC) accepted a commitment Feb. 10 from Aspen Pharmacare Holdings Ltd. to immediately drop the price of six essential cancer drugs in Europe by an average of 73% and to continue to supply the drugs for at least the next five years.
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Bamlanivimab and etesevimab

FDA grants EUA for Abcellera-Junshi-Lilly COVID-19 treatment

Feb. 10, 2021
By Lee Landenberger
Another monoclonal antibody therapy has entered the pandemic fray with the FDA granting emergency use authorization (EUA) for bamlanivimab (LY-CoV555) 700 mg and etesevimab (JS016 or LY-CoV016) 1,400 mg as a cocktail for treating mild to moderate COVID-19 in patients aged 12 and up at high risk for progressing to severe COVID-19 and/or hospitalization.
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Regulatory front for Feb. 10, 2021

Feb. 10, 2021
The latest global regulatory news, changes and updates affecting biopharma.
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Regulatory actions for Feb. 10, 2021

Feb. 10, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Abbvie, Adaptive Phage, AIM Immunetech, Astrazeneca, Biontech, Eli Lilly, I-Mab, Merck, Panbela, Pfizer, RDIF, Regeneron, Sanifit, Sanofi, Takeda, Vico.
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