Marketing authorisation application for CT001 has been submitted to the EMA for acute pain management in children

14 August 2025 - The marketing authorisation application for CT001 is submitted to the EMA for acute pain management in ...

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US FDA approves new Biktarvy indication for people with HIV who are treatment experienced and restarting antiretroviral treatment

30 July 2025 -  Gilead Sciences today announced that the US FDA has granted a new approval for a novel ...

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Vertex announces marketing authorisation in Canada for Alyftrek, a once daily next generation CFTR modulator for the treatment of cystic fibrosis

22 July 2025 - Approximately 3,800 people in Canada are now eligible for Alyftrek, with up to 60 people potentially ...

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Trixeo Aerosphere receives positive EU CHMP opinion as first inhaled medicine using next-generation propellant with near-zero Global Warming Potential

25 July 2025 - Next-generation propellant offers 99.9% reduction in global warming potential compared to current propellants. ...

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Vertex announces broad reimbursement agreement with NHS England for Alyftrek (deutivacaftor/tezacaftor/vanzacaftor) an innovative once daily CFTR modulator for the treatment of cystic fibrosis

14 July 2025 - All eligible people with cystic fibrosis in England can now benefit from this medicine - ...

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Vertex Announces European Commission approval of Alyftek, a new once daily CFTR modulator for the treatment of cystic fibrosis

1 July 2025 - Approximately 31,000 people with cystic fibrosis in the EU are now eligible for this new highly ...

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Australians with cystic fibrosis benefit from life changing expanded listing

24 June 2025 - More Australians living with cystic fibrosis will have affordable access to a life changing treatment option ...

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‘Barriers lifted’: cystic fibrosis treatment reaches final waiting patients

23 June 2025 - Ex-Wallabies player Nathan Charles has lived with cystic fibrosis for decades.  ...

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Xediton Pharmaceuticals announced today the Canadian approval and availability of Vabomere (meropenem-vaborbactam) in Canada

12 June 2025 - Xediton Pharmaceuticals is proud to announce that Vabomere (meropenem-vaborbactam) has been approved by Health Canada and ...

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US FDA approves expanded indication for AbbVie's Mavyret (glecaprevir/pibrentasvir) as first and only treatment for people with acute hepatitis C virus

11 June 2025 -  AbbVie today announced that the US FDA approved a label expansion for Mavyret (glecaprevir/pibrentasvir), an oral ...

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George Medicines announces FDA approval of Widaplik (telmisartan, amlodipine and indapamide), a new single pill combination treatment for hypertension in adults, including initial treatment

9 June 2025 - Commercialisation planning underway with US launch anticipated Q4, 2025. ...

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Trixeo Aerosphere approved in the UK as first inhaled respiratory medicine using next-generation propellant with near zero global warming potential

11 May 2025 - Trixeo Aerosphere, AstraZeneca’s fixed-dosed triple-combination therapy for COPD, is the Company’s first medicine to transition to ...

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Vertex receives CHMP positive opinion for Alyftrek, a new once-daily CFTR modulator for the treatment of cystic fibrosis

28 April 2025 - In head-to-head clinical trials, deutivacaftor/tezacaftor/vanzacaftor was non-inferior on ppFEV1 and superior compared to Kaftrio (ivacaftor/tezacaftor/elexacaftor) at ...

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European Commission approves expanded label for Kaftrio in combination with ivacaftor for people with cystic fibrosis

7 April 2025 - Approximately 4,000 people living with cystic fibrosis in the European Union are newly eligible for a ...

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Vertex announces UK MHRA approval of Alyftrek (deutivacaftor/tezacaftor/vanzacaftor), a once daily next in class CFTR modulator for the treatment of cystic fibrosis

7 March 2025 - In head to head clinical trials, deutivacaftor/tezacaftor/vanzacaftor was non-inferior on ppFEV1 and further decreased sweat chloride ...

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