First generic version of Gilead’s remdesivir will be sold by a Bangladesh drug maker

22 May 2020 - A drug maker in Bangladesh has become the first company to sell a generic version of ...

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Inside the science: companies racing to develop a COVID-19 vaccine

25 May 2020 - Even as some states move to ease the lockdowns that have cost tens of millions of ...

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WHO pauses trial of hydroxychloroquine in COVID-19 patients due to safety concerns

26 May 2020 - The World Health Organisation has suspended testing the malaria drug hydroxychloroquine in COVID-19 patients due to ...

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TGA approves Rozlytrek

25 May 2020 - Roche secures TGA approval for another cancer medicine. ...

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How the world’s premier public health agency was handcuffed

23 May 2020 - The CDC has been absent with leave during the spread of COVID-19. ...

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Fresenius Kabi’s regulatory submission for pegfilgrastim biosimilar accepted for review by EMA

22 May 2020 - Fresenius Kabi announced today that the EMA has accepted for review the company’s marketing authorisation application for ...

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U.S. is ahead of China in vaccine race, former FDA chief says

24 May 2020 - Data on Chinese vaccines in clinical development “didn’t look overwhelmingly strong,” Scott Gottlieb said. ...

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Federal scientists finally publish remdesivir data

23 May 2020 - A clinical trial led to the authorisation of the only drug shown to work in COVID-19 patients. ...

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FDA shuffles longtime division head, Janet Woodcock, to focus exclusively on COVID-19 vaccine project

22 May 2020 - FDA stalwart Janet Woodcock will temporarily step aside as the director of the agency’s Center for ...

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Hikma receives FDA approval for its generic Vascepa

22 May 2020 - Hikma Pharmaceuticals today announces that its wholly owned U.S. subsidiary Hikma Pharmaceuticals USA Inc. has received ...

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Zealand Pharma announces FDA acceptance of new drug application for the dasiglucagon HypoPal rescue pen for treatment of severe hypoglycemia

22 May 2020 - PDUFA target action date scheduled for 27 March 2021. ...

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U.S. FDA approves Takeda’s Alunbrig (brigatinib) as a first-line treatment option for patients diagnosed with rare and serious form of lung cance

22 May 2020 - Long-term results from the Phase 3 ALTA 1L trial established Alunbrig as a superior first-line treatment compared ...

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Intercept provides regulatory update

22 May 2020 - Intercept Pharmaceuticals today announced that based on discussions earlier this week, the U.S. FDA has notified Intercept ...

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U.S. FDA approves Evofem Biosciences' Phexxi (lactic acid, citric acid and potassium bitartrate), the first and only non-hormonal prescription gel for the prevention of pregnancy

22 May 2020 - A new class of female-controlled birth control for use in-the-moment. ...

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Orphazyme’s arimoclomol receives US fast track designation in amyotrophic lateral sclerosis

22 May 2020 - Orphazyme announces that the Company has received fast track designation from the US FDA for the development ...

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