FDA grants fast track designation to NS-229 for the treatment of eosinophilic granulomatosis with polyangiitis

9 September 2025 - NS Pharma, a subsidiary of Nippon Shinyaku, announced today that the US FDA has granted fast track ...

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Health Canada approves Bylvay (odevixibat) for the treatment of cholestatic pruritus in patients with Alagille syndrome

9 Settember 2025 - Bylvay is the first and only medication approved in Canada for the treatment of both Alagille ...

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ICER releases draft evidence report on treatments for obesity

9 September 2025 - Public comment period now open until 6 October 2025; requests to make oral comment during public ...

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FDA approves gemcitabine intravesical system for non-muscle invasive bladder cancer

9 September 2025 - Today, the FDA approved gemcitabine intravesical system (Inlexzo, Janssen) for adults with Bacillus Calmette-Guérin unresponsive non-muscle ...

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Revisiting the FDA’s accelerated approval pathway

8 September 2025 - After aducanumab’s accelerated approval for Alzheimer's disease, and prompted by long standing concerns regarding the accelerated approval pathway ...

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Saol Therapeutics receives complete response letter from FDA for SL1009 (DCA) for the treatment of pyruvate dehydrogenase complex feficiency

8 September 2025 - Saol is seeking a path forward with the FDA that does not require an additional trial ...

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Reimbursement delay leaves Korean patients waiting for Padcev-Keytruda first-line therapy

8 September 2025 - The first-line combination therapy of Padcev and Keytruda for metastatic urothelial carcinoma was not even submitted ...

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ICER publishes evidence report on treatment for non-cystic fibrosis bronchiectasis

8 September 2025 - There are significant uncertainties regarding long term efficacy of brensocatib; ICER estimates that treatment would achieve ...

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SMC - September 2025 decisions

8 September 2025 - The SMC has today published advice on two medicines. ...

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FDA announces real-time release of complete response letters, posts previously unpublished batch of 89

4 September 2025 - The US FDA today announced that it will release future complete response letters promptly after they are ...

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Sol-Gel announces Health Canada approval of Epsolay

4 September 2025 - - Sol-Gel Technologies announced today that on 27 August 2 2025 Health Canada issued a Notice ...

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Accrufer assigned priority review in the US by FDA in children with iron deficiency anaemia

4 September 2025 - Pending successful review, approval in the US is anticipated in 2026. ...

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DoH publishes agenda for November 2025 PBAC meeting (version 3)

5 September 2025 - The DoH has published a revised agenda for the November 2025 PBAC meeting. ...

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US FDA approves Henlius and Organon’s Bildyos (denosumab-nxxp) and Bilprevda (denosumab-nxxp), biosimilars to Prolia (denosumab) and Xgeva (denosumab), respectively

2 September 2025 - Shanghai Henlius Biotech and Organon today announced the US FDA has approved Bildyos (denosumab-nxxp) injection 60 mg/mL ...

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Ulcerative colitis: comparative study provides important insights

2 September 2025 - The data show no additional benefit of guselkumab compared to golimumab. ...

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