Tryngolza (olezarsen) approved in the European Union for familial chylomicronaemia syndrome

19 September 2025 - Sobi and Ionis Pharmaceuticals today announced that Tryngolza (olezarsen) has been approved in the European Union ...

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FDA approves pembrolizumab and berahyaluronidase alfa-pmph for subcutaneous injection

19 September 2025 - Today, the FDA approved pembrolizumab and berahyaluronidase alfa-pmph (Keytruda Qlex, Merck) for subcutaneous injection for adult ...

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Biocon Biologics receives US FDA approval for Bosaya and Aukelso, denosumab biosimilars

17 September 2025 - Biocon Biologics today announced that the US FDA has approved Bosaya (denosumab-kyqq) 60 mg/mL injection for subcutaneous ...

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Vorasidenib approved to treat patients 12 years and older with grade 2 astrocytoma or oligodendroglioma with a susceptible IDH1 or IDH2 mutation

16 September 2025 - The MHRA has today approved the medicine vorasidenib (Voranigo). ...

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Biogen receives European Commission approval for Zurzuvae (zuranolone), the first and only treatment approved for women with postpartum depression in Europe

17 September 2025 - The EC approval of Zurzuvae is based on the SKYLARK study, which demonstrated rapid relief from depressive ...

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Corstasis Therapeutics announces FDA approval of Enbumyst (bumetanide nasal spray) for the treatment of oedema associated with congestive heart failure, liver disease and kidney disease

15 September 2025 - Enbumyst is the first and only intranasal loop diuretic approved in the US offering a self-administered alternative ...

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Hundreds of people set to benefit after life-extending lung cancer treatment given green light

16 September 2025 - Targeted immunotherapy found to significantly increase overall survival rates for people with an aggressive form of lung ...

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EU approval makes Novo Nordisk’s oral semaglutide the first and only oral GLP-1 RA to reduce cardiovascular death, heart attack and stroke

15 September 2025 - This approval is based on results from the SOUL clinical trial, where oral semaglutide (Rybelsus) reduced ...

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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 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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Review panel backs expanded indications for Keytruda, Dupixent; Imfinzi sent for reconsideration

5 September 2025 - HIRA's Pharmaceutical Reimbursement Evaluation Committee (PREC) has determined that the expanded indications for MSD's immuno-oncology drug ...

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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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