Bristol Myers Squibb receives European Commission approval for Opdivo (nivolumab) as second-line treatment for unresectable advanced, recurrent or metastatic oesophageal squamous cell carcinoma

24 November 2020 - First immunotherapy to be approved for a gastro-esophageal cancer in the European Union. ...

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Australia's coronavirus vaccination program to start from March

25 November 2020 - The federal government says Australia is on track to deliver the first vaccines in March. ...

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Doctors say CDC should warn people the side effects from COVID vaccine shots won’t be ‘a walk in the park’

23 November 2020 - The CDC must be transparent about the side effects people may experience after getting their first shot ...

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Lilly and the Government of Canada sign an agreement for the supply of bamlanivimab to treat COVID-19 in Canada

24 November 2020 - Bamlanivimab is a SARS-CoV-2-neutralising antibody that emerged from the collaboration between Lilly and Vancouver-based AbCellera. ...

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PolyPid granted breakthrough therapy designation from FDA for D-PLEX for the prevention of surgical site infections in colorectal surgery

24 November 2020 - PolyPid Ltd today announced that D-PLEX100 has received breakthrough therapy designation from the U.S. FDA for the ...

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ObsEva submits marketing authorisation application to the European Medicines Agency for Yselty (linzagolix) for the treatment of women with uterine fibroids

24 November 2020 - If approved, linzagolix will be the only GnRH antagonist with flexible dose regimen options for the management ...

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Telix new drug application for prostate cancer imaging product accepted by US FDA

24 November 2020 - Telix Pharmaceuticals announces new drug application for TLX591-CDx. ...

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Success for a third—and perhaps most important—COVID-19 vaccine

23 November 2020 - The AstraZeneca-Oxford jab is likely to be widely used around the world. ...

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Merck submits applications for licensure of V114, the company’s investigational 15 valent pneumococcal conjugate vaccine, for use in adults to the US FDA and EMA

23 November 2020 - Merck today announced the company has submitted applications to the US FDA and EMA for licensure of ...

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FDA approves first drug to treat rare metabolic disorder

23 November 2020 - Today, the U.S. FDA approved Oxlumo (lumasiran) as the first treatment for primary hyperoxaluria type 1, a ...

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Rigel and Medison announce Health Canada approval of Tavalisse, an oral medication for the treatment of adults with chronic immune thrombocytopenia

23 November 2020 - Rigel Pharmaceuticals and Medison Pharma today announced that Health Canada has approved the new drug submission ...

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VBI Vaccines announces submission of marketing authorisation application for 3 antigen prophylactic hepatitis B vaccine to the European Medicines Agency

23 November 2020 -VBI Vaccines today announced the submission of a marketing authorisation application to the EMA for the Company’s ...

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Workshop on regulatory support for development of orphan medicines

23 November 2020 - On Monday, 30 November, EMA is hosting a workshop to discuss the benefits and impact of ...

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COVID-19 shots could reach first Americans by mid-December, top health official says

23 November 2020 - U.S. health care workers and others recommended for the nation’s first COVID-19 inoculations could start getting shots ...

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Theralase granted FDA fast track designation for NMIBC Phase 2 clinical study

23 November 2020 - Theralase Technologies announced today that the U.S. FDA has granted Theralase fast track designation for its ...

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