Provention Bio completes rolling submission of the biologics license application for teplizumab for the delay or prevention of clinical type 1 diabetes in at risk individuals

2 November 2020 - Submission of chemistry, manufacturing and controls and administrative information modules represent completion of the Company's submission for ...

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Janssen submits paliperidone palmitate 6 month supplemental new drug application to U.S. FDA for treatment of schizophrenia in adults

2 November 2020 - If approved, paliperidone palmitate 6 month will be the first and only long-acting injectable schizophrenia treatment with a ...

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Takeda price hikes for a GI drug may give some patients another kind of stomachache

2 November 2020 - Two weeks ago, Takeda Pharmaceuticals raised the list price of its Entyvio treatment for ulcerative colitis ...

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FDA approves Bronchitol for US market

2 November 2020 - Pharmaxis to manufacture product and export to USA. ...

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The FDA’s Digital Health Center Of Excellence: why it matters and what it means to you

29 October 2020 - Last month, the US FDA launched the Digital Health Center of Excellence, bolstering the shift toward digital ...

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A CDER study of factors that may predict the likelihood of generic drug marketing applications

28 October 2020 - The investigators compiled proprietary data related to abbreviated new drug applications and other internal or public ...

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Gilead’s COVID-19 drug is mediocre. It will be a blockbuster anyway.

29 October 2020 - Gilead Sciences said Wednesday that remdesivir, which has been authorised for emergency use since the spring, brought ...

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Social media disinformation campaigns tied to vaccine hesitancy

29 October 2020 - Social media disinformation campaigns designed to cast doubt on the safety and effectiveness of vaccines are contributing ...

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How will a COVID vaccine be distributed once it's approved by FDA?

29 October 2020 - Distributing the first wave of doses will be a massive undertaking. ...

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The FDA will not inspect vaccine production plants

29 October 2020 - Approval of a vaccine by the FDA typically requires inspection of the vaccine’s manufacturing plants.  ...

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Roche receives FDA approval for the cobas EGFR Mutation Test v2 as the first companion diagnostic test for expanded EGFR TKI therapies in patients with non-small cell lung cancer

29 October 2020 - The new FDA approval allows the test to be used as a companion diagnostic for a broad ...

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FDA accepts for priority review Libtayo (cemiplimab-rwlc) for advanced non-small cell lung cancer with PD-L1 expression of ≥50%

29 October 2020 - Regeneron Pharmaceuticals today announced that the U.S. FDA has accepted for priority review the supplemental biologics license ...

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reVision Therapeutics announces US FDA grant of rare paediatric disease and orphan drug designation for REV-0100 for the treatment of Stargardt disease

28 October 2020 - reVision Therapeutics today announced that the US FDA has granted the Company's request to designate REV-0100 as ...

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Passage Bio’s PBKR03 receives orphan drug and rare paediatric disease designations from FDA for treatment of Krabbe disease

28 October 2020 - Passage Bio today announced that the U.S. FDA has granted orphan drug and rare paediatric disease designations ...

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Astellas receives U.S. FDA fast track designation for ASP5354, an investigational near-infrared fluorescence imaging agent

28 October 2020 - Astellas Pharma announced today that the US FDA has granted fast track designation based on non-clinical and ...

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