scPharmaceuticals announces FDA approval of supplemental new drug application expanding the Furoscix indication to include the treatment of oedema in patients with chronic kidney disease

6 March 2025 - Furoscix is expected to be available for chronic kidney disease patients in April 2025. ...

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Neurotech’s Encelto (revakinagene taroretcel-lwey) approved by the FDA for the treatment of macular telangiectasia type 2

6 March 2025 - Encelto is the first and only FDA approved treatment for macular telangiectasia type 2. ...

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FDA accepts supplemental biologics license application for Roche’s Gazyva/Gazyvaro for the treatment of lupus nephritis

5 March 2025 - The filing application is based on data from the Phase 3 REGENCY study, where Gazyva/Gazyvaro showed superiority ...

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Tevimbra approved in US for first-line treatment of advanced oesophageal squamous cell carcinoma in combination with chemotherapy

4 March 2025 - New indication based on results from a global Phase 3 trial demonstrating significantly improved overall survival ...

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Skyrizi (risankizumab) now available for moderately to severely active ulcerative colitis, expanding AbbVie's portfolio across inflammatory bowel disease

4 March 2025 - Skyrizi is the first IL-23 specific inhibitor approved for both moderate to severe ulcerative colitis and ...

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Capricor Therapeutics announces FDA acceptance and priority review of its biologics license application for deramiocel to treat Duchenne muscular dystrophy

4 March 2025 - FDA assigns PDUFA target action date of 31 August 2025. ...

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Celltrion receives US FDA approval for Stoboclo (denosumab-bmwo) and Osenvelt (denosumab-bmwo) biosimilars referencing Prolia and Xgeva

3 March 2025 - The FDA approval is based on robust clinical evidence, which show no clinically meaningful differences from the ...

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Amneal’s BLA submissions for two denosumab biosimilars accepted for review by US FDA

3 March 2025 - Denosumab biosimilar candidates reference Prolia and Xgeva. ...

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FDA files Corcept’s new drug application for relacorilant as treatment for patients with hypercortisolism

3 March 2025 - FDA assigns a PDUFA target action date of 30 December 2025. ...

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Qalsody (tofersen injection) receives conditional marketing authorisation from Health Canada as the first ALS treatment targeting a genetic cause

3 March 2025 - Biogen's second rare disease therapy to be approved in Canada reflects a continued commitment to advancing ...

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Depemokimab applications accepted for review by the US FDA for asthma with type 2 inflammation and for chronic rhinosinusitis with nasal polyps

3 March 2025 - Submissions based on data from positive SWIFT and ANCHOR trials. ...

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Latigo Biotherapeutics granted FDA fast track designation for LTG-001, potential best in class Nav1.8 inhibitor for the non-opioid treatment of acute pain

3 March 2025 - LTG-001 demonstrated favourable safety and tolerability profile with predictable pharmacokinetics in Phase 1 trial. ...

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TGA decides not to register lecanemab in Australia

3 March 2025 - BioArctic's partner Eisai announced today that the TGA has declined the approval of lecanemab as a treatment ...

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FDA approves Genentech’s TNKase in acute ischaemic stroke in adults

3 March 2025 - TNKase (tenecteplase) is the first stroke medicine approved by the FDA in nearly 30 years. ...

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Imfinzi-based perioperative regimen recommended for approval in the EU by CHMP for resectable non-small cell lung cancer

3 March 2025 - Recommendation based on AEGEAN Phase 3 trial results which showed Imfinzi reduced the risk of recurrence, ...

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