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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RSV prophylaxis with nirsevimab: benefits for healthy children in the first RSV season

2 June 2025 - Children immunised with the antibody nirsevimab are significantly less likely to develop RSV-related lower respiratory tract infections. ...

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Garadacimab in hereditary angioedema: evidence of considerable additional benefit

2 June 2025 - An indirect comparison shows a significant reduction in the monthly rate of attacks and other benefits.  ...

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Enhertu (trastuzumab deruxtecan) receives time limited reimbursement recommendation from Canada's Drug Agency for gastric cancer

23 May 2025 - AstraZeneca and Daiichi Sankyo are pleased to announce that Canada's Drug Agency has issued a time-limited reimbursement ...

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FDA accepts TransCon CNP NDA for priority review

2 June 2025 - Ascendis Pharma today announced that the US FDA has accepted for priority review its new drug application ...

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Kura Oncology and Kyowa Kirin announce FDA acceptance and priority review of new drug application for ziftomenib in adults with relapsed or refractory NPM1 mutant AML

1 June 2025 - New drug application based on positive results from the Phase 2 KOMET-001 trial. ...

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Schedule of Pharmaceutical Benefits - 1 June 2025

1 June 2025 - The June 2025 issue of the Schedule of Pharmaceutical Benefits is out and now in effect. ...

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Moderna receives US FDA approval for COVID-19 vaccine mNEXSPIKE

31 May 2025 - mNEXSPIKE becomes Moderna's third FDA approved product. ...

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Zydus receives US FDA fast track designation for usnoflast, a novel oral NLRP3 inhibitor, for the treatment of amyotrophic lateral sclerosis

28 May 2025 - Usnoflast has previously also received orphan drug designation from the US FDA. ...

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Capsida receives FDA fast track designation for its potential first in class IV administered gene therapy for STXBP1 developmental and epileptic encephalopathy

29 May 2025 - Capsida previously received FDA orphan drug designation and IND clearance to initiate the SYNRGY Phase 1/2a ...

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ICER publishes evidence report on treatment for secondary progressive multiple sclerosis

29 May 2025 - There are significant uncertainties regarding long term efficacy of tolebrutinib; ICER estimates that treatment would achieve ...

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Patritumab deruxtecan biologics license application for patients with previously treated locally advanced or metastatic EGFR mutated non-small cell lung cancer voluntarily withdrawn

29 May 2025 - The biologics license application seeking accelerated approval in the US for Daiichi Sankyo and Merck's patritumab ...

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Eton Pharmaceuticals announces US FDA approval for Khindivi (hydrocortisone) oral solution

28 May 2025 - Commercial launch expected the week of 2 June 2025. ...

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Pfizer and BioNTech submit EMA application for COVID-19 vaccine targeting LP.8.1 for 2025-2026 season

28 May 2025 -  2025 -- Pfizer and BioNTech today announced that they have submitted a regulatory application to the ...

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Alcon announces FDA approval of Tryptyr (acoltremon ophthalmic solution) 0.003% for the treatment of the signs and symptoms of dry eye disease

28 May 2025 - Tryptyr is a first in class TRPM8 receptor agonist that rapidly stimulates natural tear production in patients ...

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Experimental Drug Development Centre granted US FDA fast track designation for antibody-drug conjugate EBC-129 to treat pancreatic ductal adenocarcinoma

28 May 2025 - EBC-129 is the first made in Singapore antibody-drug conjugate to enter clinical development. ...

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