Enhertu type II variation application validated in the EU for previously treated patients with HER2 positive metastatic solid tumours

11 September 2025 - Submission based on three Phase 2 trials where Daiichi Sankyo and AstraZeneca’s Enhertu showed clinically meaningful ...

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Health Canada approves Slenyto - extended-release melatonin formulation - as a prescription drug for insomnia in children with autism spectrum disorder and Smith-Magenis syndrome

10 September 2025 - Neurim Pharmaceuticals is pleased to announce that Health Canada has granted marketing authorisation for Slenyto, an ...

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FDA files Corcept’s new drug application for relacorilant as a treatment for patients with platinum-resistant ovarian cancer

10 September 2025 - Corcept Therapeutics today announced that the US FDA has accepted Corcept’s new drug application for relacorilant as ...

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FDA approves selumetinib for pediatric patients 1 year of age and older with neurofibromatosis type 1 with symptomatic, inoperable plexiform neurofibromas

10 September 2025 - Today, the FDA approved selumetinib (Koselugo, AstraZeneca Pharmaceuticals) granules and capsules for paediatric patients 1 year ...

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FDA accepts biologics license application for Sobi's NASP for patients with uncontrolled gout

10 September 2025 - Sobi today announced that the US FDA has accepted the biologics license application seeking approval for Nanoecapsulated ...

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Alberta man pushes Feds to approve new Alzheimer’s drugs Leqembi and Kinsula

9 September 2025 - An Alberta man living with Alzheimer’s disease is calling on Ottawa to approve two new drugs ...

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US FDA approval of Inlexzo (gemcitabine intravesical system) set to transform how certain bladder cancers are treated

9 September 2025 - First and only drug releasing system to provide extended local delivery of a cancer medication into the ...

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Partner Therapeutics receives EMA approval of Imreplys (sargramostim, rhu GM-CSF) to treat exposure to myelosuppressive doses of radiation (haematopoietic sub-syndrome of acute radiation syndrome

9 September 2025 - Approval based upon Imreplys significantly improving survival, accelerating recovery of white blood cells and platelets, and ...

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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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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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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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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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US FDA approves expanded indication for Vonvendi [von Willebrand factor (recombinant)] for adults and children with von Willebrand disease

5 September 2025 - Takeda today announced that the US FDA has approved the supplemental biologics license application for Vonvendi [von ...

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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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