New cystic fibrosis drug fast tracked for NHS use

15 July 2025 - Some people with cystic fibrosis are set to benefit from a new once daily triple therapy treatment, ...

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Denali Therapeutics announces FDA acceptance and priority review of biologics license application for tividenofusp alfa for Hunter syndrome

7 July 2025 - FDA assigns PDUFA target action date of 5 January 2026, for decision on accelerated approval. ...

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KalVista Pharmaceuticals announces FDA Approval of Ekterly (sebetralstat), first and only oral on-demand treatment for hereditary angioedema

7 July 2025 - First new on demand hereditary angioedema treatment in over a decade, with potential to transform management of the ...

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Will miracle HIV drug go on the PBS?

5 July 2025 - A new twice yearly antiviral injection that can prevent HIV is likely to be approved soon in ...

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Garadacimab for the prevention of recurrent attacks of hereditary angioedema in patients 12 years of age and older

2 July 2025 - The Department of Health and Social Care has asked NICE to produce guidance on the use ...

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MHRA approves nogapendekin alfa inbakicept to treat adult patients with non-muscle invasive bladder cancer 

4 July 2025 - The MHRA has today approved nogapendekin alfa inbakicept (Anktiva) for adults with BCG unresponsive non-muscle invasive bladder ...

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Quebec implements public reimbursement of Pluvicto - a defining milestone for radioligand therapy in Canada

3 July 2025 - Pluvicto now publicly funded in provinces covering most Canadians, offering renewed hope to those facing progressive PSMA ...

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Vitalgen's gene therapy drug VGN-R09b for primary Parkinson's disease receives FDA fast track designation

26 June 2025 - Shanghai Vitalgen announced that its gene therapy drug, VGN-R09b, for the treatment of primary Parkinson’s disease, has ...

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Teprotumumab for the treatment of patients with thyroid eye disease

2 July 2025 - The Department of Health and Social Care has asked NICE to produce guidance on the use ...

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European Commission approves Biocon biologics’ denosumab biosimilars

3 July 2025 - Biocon Biologics today announced that the European Commission has granted marketing authorisation in the European Union ...

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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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Public Summary Documents - March 2025 PBAC meeting

4 July 2025 - The Public Summary Documents (first time decisions not to recommend and deferrals) from the March 2025 ...

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Imfinzi approved in the EU as first and only peri-operative immunotherapy for muscle-invasive bladder cancer

4 July 2025 - Approval based on NIAGARA Phase III trial results which showed a 32% reduction in the risk ...

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Jazz Pharmaceuticals receives European Commission marketing authorisation for Ziihera (zanidatamab) for the treatment of advanced HER2 positive biliary tract cancer

1 July 2025 - Conditional approval based on positive results from the HERIZON-BTC-01 Phase 2b trial. ...

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Johnson & Johnson submits application to the EMA seeking indication extension of Akeega (niraparib and abiraterone acetate dual action tablet) for the treatment of adult patients with metastatic hormone-sensitive prostate cancer and HRR gene alterations

3 July 2025 - The submission is based on results from the Phase 3 AMPLITUDE study evaluating niraparib in combination with ...

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Release of provisional recommendations for expert advisory committees

1 July 2025 - We’re improving our processes, so that people can understand the outcome of expert advice to PHARMAC earlier. ...

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