Biogen to expand access to its ALS drug, but move may come too late for some patient

27 April 2021 - After weeks of controversy, Biogen has agreed to provide an experimental drug for combating ALS to ...

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EYEMATE system for remote glaucoma management obtains FDA breakthrough device designation

28 April 2021 - - Implandata Ophthalmic Products has announced today that its game-changing EYEMATE system for digitally enabled remote patient ...

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FDA Advisory Committee votes in favour of maintaining accelerated approval of Genentech’s Tecentriq for PD-L1 positive, metastatic triple negative breast cancer

27 April 2021 - Genentech today announced the U.S. FDA Oncologic Drugs Advisory Committee voted 7 to 2 in favour of ...

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FDA begins review of GC Pharma’s blood product for marketing authorisation

27 April 2021 - The U.S. FDA has entered a full review of GC Pharma’s intravenous immunoglobulin therapy GC5107 for ...

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Takeda announces U.S. FDA grants priority review for new drug application for mobocertinib (TAK-788) as a treatment for EGFR exon 20 insertion positive metastatic non-small cell lung cancer

28 April 2021 - Prescription Drug User Fee Act target action date set for 26 October 2021. ...

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Rockwell Medical announces marketing approval of Triferic AVNU in Canada

27 March 2021 - Rockwell Medical today announced that Triferic AVNU (ferric pyrophosphate citrate injection) received a Notice of Compliance (marketing ...

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Y-mAbs submits omburtamab marketing authorisation application to the EMA

27 April 2021 - Y-mAbs Therapeutics today announced that the Company has submitted its marketing authorisation application to the European Medicines ...

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Medtronic receives FDA breakthrough designation for the Emprint ablation catheter kit

27 April 2021 - Minimally invasive option has potential to provide long-term management of lung malignancies while protecting lung function. ...

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Sol-Gel Technologies provides update on FDA review of Epsolay

27 April 2021 - Sol-Gel Technologies today announced an update regarding the U.S. FDA approval process for Epsolay (benzoyl peroxide) ...

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Enzyvant resubmits biologics licence application to FDA for RVT-802 for paediatric congenital athymia

27 April 2021 - Enzyvant today announced the resubmission of the biologics licence application to the U.S. FDA for RVT-802, ...

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Fractyl announces FDA breakthrough device designation for Revita DMR in insulin treated type 2 diabetes

27 April 2021 - REVITA-T2Di trial is underway to evaluate the effectiveness of Revita DMR in improving glucose control while reducing ...

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EMA grants accelerated assessment procedure for Nefecon for the treatment of IgA nephropathy

23 April 2021 - Calliditas Therapeutics today announced that its lead product candidate Nefecon, a novel oral formulation targeting down regulation ...

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FDA guidance says sponsors should provide 'convincing' proof of concept data to support INDs for individualised medicine

26 April 2021 - Recent draft guidance from the US FDA addresses the non-clinical safety data to support investigational new ...

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Glenmark’s Ryaltris nasal spray now approved in Europe for the first-line treatment of allergic rhinitis in patients over 12 years of age

26 April 2021 - This marks Glenmark’s first innovative product approval in the European Union. ...

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Health Canada initiates the review of the rolling submission for the first Canadian based COVID-19 vaccine candidate

23 April 2021 - Medicago is pleased to announce that Health Canada received for review the first portion of Medicago’s ...

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