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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Extra transparency measures for COVID-19 vaccines and therapeutics

30 October 2020 - Today the EMA has implemented two further extra transparency measures for COVID-19 medicines, by publishing both ...

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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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European Patent Office rules in favour of Sanofi and Regeneron concerning Praluent (alirocumab)

29 October 2020 - Ruling invalidates Amgen’s European patent claims directed to PCSK9 antibodies relevant to Praluent (alirocumab). ...

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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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European Commission grants marketing authorisation for Arikayce liposomal 590 mg nebuliser dispersion for the treatment of NTM lung infections caused by MAC in adult non-CF patients with limited treatment options

28 October 2020 - Arikayce is the first and only therapy approved in both the European Union and United States for ...

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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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Leo Pharma is withdrawing the drug Picato (ingenol mebutate), used to treat skin lesions, due to the potential increased risk of skin cancer

27 October 2020 - At Health Canada's request, Leo Pharma is withdrawing Picato from the Canadian market.  ...

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KYE Pharmaceuticals announces commercial availability of Firdapse in Canada

28 October 2020 - KYE Pharmaceuticals today announced an important milestone, Firdapse (amifampridine phosphate), the first amifampridine product approved in Canada, ...

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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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Sanofi and GSK to support COVAX with 200 million doses of adjuvanted, recombinant protein based COVID-19 vaccine

28 October 2020 - COVAX Facility is led by Gavi and aims to secure successful and equitable access to COVID-19 vaccines ...

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