FDA approval of Leqembi subcutaneous formulation charts path to combination therapies for Alzheimer's disease

29 August 2025 - Subcutaneous delivery increases accessibility and introduces potential for at home administration, following model of diabetes and ...

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Prescription drug rices in the U.S. are 2.56 times higher than other nations – brand-named drugs 3.44 times higher

27 January 2021 - Prescription drug prices in the United States are significantly higher than in other nations, with prices ...

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M6P Therapeutics receives six rare paediatric disease designations from the U.S. FDA for company’s deep pipeline of programs for lysosomal storage disorders

28 January 2021 - U.S. FDA also grants two orphan drug designations for the company’s gene therapy programs for Gaucher disease ...

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Bio-Thera Solutions announces FDA accepts biologics license application for BAT1706, a proposed biosimilar to Avastin

28 January 2021 - Bio-Thera Solutions today announced that the U.S. FDA has accepted its biologics license application for BAT1706, a ...

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Advocacy groups urge Biden administration not to tap Woodcock as FDA commissioner

27 January 2021 - As the Biden White House attempts to fashion its health policies, a coalition of consumer and ...

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Clarification of Comirnaty dosage interval

28 January 2021 - EMA’s human medicines committee (CHMP) has updated the product information for the COVID-19 vaccine Comirnaty to ...

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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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Alberta announces funding for pricey gene therapy drug Zolgensma

Alberta Health Minister Tyler Shandro announced funding Wednesday for the gene therapy Zolgensma, which is used to treat toddlers with ...

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On the role of cost effectiveness thresholds in health care priority setting

25 January 2021 - In the past few years, empirical estimates of the marginal cost at which health care produces a ...

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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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NICE publishes final guidance on new use for Lonsurf

27 January 2021 - NICE has completed its review of trifluridine with tipiracil hydrochloride for the treatment of patients with ...

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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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Coronavirus: EU threat to Australia’s vaccine program

27 January 2021 - A European move to shore up supplies of both the Pfizer/BioNTech and Oxford/AstraZeneca vaccines looks to ...

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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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Government rejects claim overseas production issues threaten access to vaccines

27 January 2021 - The entire population could be vaccinated against COVID-19 in as little as 6½ months, meaning it's ...

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