FDA approval of Leqembi subcutaneous formulation charts path to combination therapies for Alzheimer's disease

29 August 2025 - Subcutaneous delivery increases accessibility and introduces potential for at home administration, following model of diabetes and ...

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Update on US regulatory review of Saphnelo subcutaneous administration in systemic lupus erythematosus

3 February 2026 - The US FDA issued a complete response letter regarding the biologics license application for Saphnelo (anifrolumab) for ...

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Datroway granted priority review in the US as first-line treatment for patients with metastatic triple negative breast cancer who are not candidates for immunotherapy

3 February 2026 - Daiichi Sankyo and AstraZeneca’s supplemental biologics license application for Datroway (datopotamab deruxtecan-dlnk) has been accepted and ...

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MoonLake announces FDA fast track designation for sonelokimab palmoplantar pustulosis

2 February 2026 - MoonLake Immunotherapeutics today announces that the FDA has granted fast track designation for sonelokimab for the treatment ...

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Donanemab in early Alzheimer's disease: important questions remain unanswered

30 January 2026 - For the treatment of Alzheimer's disease, it is crucial to distinguish between those with mild cognitive ...

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Aquestive Therapeutics announces FDA issuance of complete response letter for Anaphylm

2 February 2026 - Deficiencies limited to packaging and administration. ...

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Imfinzi perioperative raegimen recommended for approval in the EU by CHMP for patients with early gastric and gastro-oesophageal cancers

2 February 2026 - Recommendation based on MATTERHORN Phase III trial results which showed a 29% reduction in the risk of ...

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Call for access to improve quality of life for thyroid cancer survivors

2 February 2026 - A TGA approved drug that prevents kidney failure in thyroid cancer survivors remains inaccessible. ...

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Chiesi Global Rare Diseases and Protalix BioTherapeutics receive positive CHMP opinion for an additional dosing regimen of 2 mg/kg body weight every four weeks for Elfabrio (pegunigalsidase alfa) in the EU

30 January 2026 - Chiesi Global Rare Diseases and Protalix BioTherapeutics today announced an update on pegunigalsidase alfa. ...

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Samsung Bioepis to launch Eylea biosimilar Opuviz in Europe

30 January 2026 - Samsung Bioepis said Friday it has reached an agreement with US based firm Regeneron and Germany’s ...

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Pharming Group receives complete response letter from US FDA for sNDA for Joenja (leniolisib) in children aged 4 to 11 years with APDS

1 February 2026 - Pharming today announced that the US FDA has issued a complete response letter to its supplemental ...

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Cheaper medicines to help men fight prostate cancer

1 February 2026 - From today, Australians with an aggressive form of prostate cancer will have access to cheaper medicines ...

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Ultragenyx resubmits biologics license application for UX111 AAV gene therapy to treat Sanfilippo syndrome type A (MPS IIIA) to US FDA

30 January 2026 - Company expects up to six month review period per FDA guidelines. ...

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New Zealand Pharmaceutical Schedule - 1 February 2026

1 February 2026 - The February 2026 issue of the New Zealand Pharmaceutical Schedule is now available and in effect. ...

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Sanofi’s Rezurock recommended for EU approval by the CHMP to treat chronic graft vs host disease

30 January 2026 - The EMA’s CHMP has adopted a positive opinion recommending the conditional marketing authorisation of Rezurock (belumosudil) in ...

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Schedule of Pharmaceutical Benefits - 1 February 2026

1 February 2026 - The February 2026 issue of the Schedule of Pharmaceutical Benefits is out and now in effect. ...

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