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BioWorld - Monday, July 20, 2026
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Regulatory front

U.S. priorities set for first round of COVID-19 vaccines

Dec. 2, 2020
By Mari Serebrov
The latest global regulatory news, changes and updates affecting biopharma, including: Canada moves to make some COVID-19 flexibilities permanent; Industry group forms to advance subcutaneous technology.
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Regulatory actions for Dec. 2, 2020

Dec. 2, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Ascentage, Biontech, Catalyst, Elusys, Kempharm, LG Chem, Mesoblast, Oyster Point, Pfizer, Protagonist, Regent, Telix, Vanda, Wanbang.
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Hetlioz approved in U.S. for nighttime sleep disturbances in Smith-Magenis syndrome

Dec. 2, 2020

FDA grants accelerated approval to Gavreto for advanced or metastatic RET-altered thyroid cancers

Dec. 2, 2020
FDA Approved stamp

Cerus wins FDA approval of Intercept blood system

Dec. 1, 2020
By Meg Bryant
Cerus Corp. has received the green light from the U.S. FDA for its Intercept blood system for cryoprecipitation. The device, which garnered a breakthrough device designation in 2018, is used to produce Pathogen Reduced Cryoprecipitated Fibrinogen Complex (PR-Cryo) for treating and controlling bleeding, including massive hemorrhage, associated with fibrinogen deficiency.
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Regulatory front

FDA updates Baxter infusion pump recall

Dec. 1, 2020
By Mark McCarty
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: GAO, National Academies report on AI in health care; Commerce begins assessment of U.S. drug, device manufacturing base.
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Regulatory actions for Dec. 1, 2020

Dec. 1, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Bearpac Medical, Hologic.
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Mental illness illustration

Minerva shares marred by FDA feedback on schizophrenia program

Dec. 1, 2020
By Michael Fitzhugh
Investors in Minerva Neurosciences Inc. on Dec. 1 gave a chilly reception to reported FDA feedback on the company's experimental treatment for the negative symptoms in schizophrenia, roluperidone. Though the drug failed to deliver statistically significant differences vs. placebo in a phase III study this year, CEO Remy Luthringer outlined a potential path to NDA filing for the candidate using a modified intent-to-treat analysis of the trial and evidence from other ongoing evaluations.
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Coronavirus and syringes

Moderna seeks EUA for COVID-19 vaccine, reports 100% efficacy against severe disease

Dec. 1, 2020
By Michael Fitzhugh
Moderna Inc., late on Nov. 30, said it has asked the FDA to bless emergency use of its COVID-19 vaccine mRNA-1273 after phase III data confirmed it to be 94.1% effective in preventing symptomatic cases of the disease and 100% effective in preventing severe cases. The Cambridge, Mass.-based company said efficacy was "consistent across age, race and ethnicity and gender demographics."
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Regulatory front

Commerce begins assessment of U.S. drug, device manufacturing base

Dec. 1, 2020
By Mari Serebrov
The latest global regulatory news, changes and updates affecting biopharma, including: HIV trial networks streamlined; Grants to advance use of RWD, RWE; GAO, National Academies, report on AI in health care; ICER not sold on roxadustat; Teva, Cephalon latest EC targets; Hungary looks to Russian vaccine.
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