FDA grants accelerated approval to naxitamab for high-risk neuroblastoma in bone or bone marrow

25 November 2020 - On 24 November 2020, the FDA granted accelerated approval to naxitamab (Danyelza, Y-mAbs Therapeutics) in combination with ...

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RhoVac's prostate cancer drug candidate RV001 is granted fast track designation by the FDA

25 November 2020 - RhoVac, a clinical stage company today announced that the American FDA has granted Fast Track Designation to ...

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AstraZeneca gears up to vaccinate the world against COVID-19

24 November 2020 - Among the front-runners racing to deliver a COVID-19 shot, has the least vaccine experience. But it has ...

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Liquidia receives complete response letter from FDA for LIQ861 (treprostinil) inhalation powder for the treatment of pulmonary arterial hypertension

25 November 2020 - Complete response letter does not cite need for additional clinical studies. ...

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Remdesivir (Veklury) approval for the treatment of COVID-19—the evidence for safety and efficacy

26 November 2020 - Under FDA law, approval of a new drug requires substantial evidence of effectiveness and a demonstration of ...

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Medical trial delays see Australians wait for rare disease treatment

25 November 2020 - Patients with rare diseases are entering ‘random lottery’ draws for clinical trials because Australia is too slow ...

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Third major COVID-19 vaccine shown to be effective and cheaper

24 November 2020 - Drugmaker AstraZeneca said late-stage trials showed its COVID-19 vaccine is highly effective, buoying the prospects of a ...

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Pfizer vaccine distribution could kick off within weeks pending FDA approval, Azar says

24 November 2020 - A FDA panel will meet on 10 December to consider Pfizer’s emergency use authorisation application for its ...

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EU drug regulator could rule on COVID-19 vaccines by year end

24 November 2020 - The EMA could produce a scientific opinion on COVID-19 vaccines seeking regulatory approval by the end ...

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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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