TGA to rule on psychedelic drug access for mental health problems

28 January 2021 - A group of prominent Australians is continuing to push for greater access to psychedelic drugs to ...

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E.U. and U.K. fighting over scarce vaccines

27 January 2021 - As vaccine production falls behind schedule, and the European Union lags in inoculating people, Brussels and London ...

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EU demands UK made AstraZeneca vaccine doses

27 January 2021 - The EU has urged pharmaceutical firm AstraZeneca to supply it with more doses of its COVID-19 ...

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European Medicines Agency accepts GBT’s marketing authorisation application for Oxbryta (voxelotor) for the treatment of haemolytic anemia in sickle cell disease

27 January 2021 - Global Blood Therapeutics today announced that the EMA has completed the validation of GBT’s marketing authorisation application ...

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Australia’s COVID-19 vaccine information campaign begins

27 January 2021 - The Australian Government’s $23.9 million public information campaign to encourage Australians to get a COVID-19 vaccine begins ...

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European Commission approves Keytruda (pembrolizumab) as first-line treatment in adult patients with metastatic microsatellite instability-high or mismatch repair deficient colorectal cancer

26 January 2021 - Keytruda is first checkpoint inhibitor approved in Europe to treat MSI-H or dMMR colorectal cancer. ...

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Alleviant Medical receives breakthrough device designation from FDA for transcatheter technology

25 January 2021 - Alleviant Medical today announced that the US FDA has granted the company a breakthrough device designation ...

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PEDRA Technology receives FDA breakthrough device designation for its PEDRA Xauron real-time tissue perfusion system

25 January 2021 - Novel perfusion monitor achieves FDA breakthrough device Designation for real-time, peri-procedural monitoring of tissue perfusion in patients ...

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Scott Morrison says Australia will not be a hostage to global vaccine shortages

26 January 2021 - Scott Morrison has revealed why Australia won’t be “completely hostage” to overseas vaccine schedules and shortages. ...

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MeiraGTx announces AAV-CNGA3 granted fast track designation by U.S. FDA for treatment of achromatopsia

26 January 2021 - MeiraGTx today announced that the U.S. FDA has granted fast track designation to its AAV-CNGA3 gene therapy ...

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Recordati Rare Diseases: Carbaglu (carglumic acid) receives U.S. FDA approval for a new indication to treat acute hyperammonaemia associated with propionic acidemia and methylmalonic acidemia

26 January 2021 - Carbaglu is first and only FDA approved medication for hyperammonaemia associated with these rare conditions. ...

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Vertex announces U.S. FDA acceptance of supplemental new drug application for Trikafta (elexacaftor/tezacaftor/ivacaftor and ivacaftor) in children with cystic fibrosis ages 6 through 11 with certain mutations

26 January 2021 - FDA grants priority review of the application and sets a PDUFA target action date of 8 June ...

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FDA approves Theranica's Nerivio for acute treatment of migraine in adolescents

25 January 2021 - Theranica today announced that its Nerivio therapeutic device has received the FDA clearance to market for ...

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Albireo announces U.S. FDA acceptance of new drug application for odevixibat

25 January 2021 - FDA has granted odevixibat fast track, rare paediatric disease and orphan drug designations. ...

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Iterum Therapeutics announces U.S. FDA filing acceptance of new drug application for oral sulopenem

25 January 2021 - If approved, first oral penem in the U.S. and first new oral treatment for uUTIs in over ...

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