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 ...

Read more →

Cogent Biosciences announces submission of new drug application for bezuclastinib in non-advanced systemic mastocytosis

30 December 2025 - Cogent Biosciences today announced it has submitted its new drug application to the US FDA for ...

Read more →

Ultragenyx completes rolling submission of biologics license application to US FDA for DTX401 AAV gene therapy for glycogen storage disease type Ia

30 December 2025 - If approved, DTX401 will be the first therapy approved to treat the underlying cause of glycogen storage ...

Read more →

Vanda Pharmaceuticals announces FDA approval of Nereus (tradipitant) for the prevention of vomiting induced by motion: a historic scientific milestone in the prevention of motion sickness

30 December 2025 - Vanda Pharmaceuticals today announced that the US FDA has approved Nereus (tradipitant), an oral neurokinin-1 receptor antagonist, ...

Read more →

PBS Expenditure and Prescriptions Report (2024-25)

22 December 2025 - The PBS Expenditure and Prescriptions Report 1 July 2024 to 30 June 2025 is now available. ...

Read more →

FDA accepts for review Inovio's BLA for INO-3107 for the treatment of adults with recurrent respiratory papillomatosis

29 December 2025 - Inovio today announced that the US FDA accepted the company's biologics license application for INO-3107 for ...

Read more →

Unicycive Therapeutics announces resubmission of new drug application for oxylanthanum carbonate

29 December 2025 - New PDUFA date expected in 1H 2026 within 30 days of NDA resubmission. ...

Read more →

Praxis Precision Medicines announces the FDA has granted breakthrough therapy designation for ulixacaltamide hydrochloride in essential tremor

29 December 2025 - The breakthrough therapy designation was granted based on the positive top-line results from the Essential3 Phase 3 ...

Read more →

US FDA approves Agios’ Aqvesme (mitapivat) for the treatment of anaemia in adults with alfa or beta-thalassaemia

23 December 2025 - Aqvesme expected to be available in late January 2026, following Aqvesme REMS program implementation. ...

Read more →

Drug makers push back against government’s generic price cut plan

28 December 2025 - Pharma industry warns lower generic prices will curb R&D, health officials cite unchanged pricing since 2012. ...

Read more →

Amneal announces FDA approval of denosumab biosimilars referencing Prolia and Xgeva

22 December 2025 - Company expects to commercialize six biosimilars across eight presentations by 2027. ...

Read more →

Korea to expand Keytruda reimbursement to 11 new cancer uses starting 2026

24 December 2025 - Korea’s national health insurance program will broaden reimbursement for MSD’s blockbuster PD-1 inhibitor Keytruda in a ...

Read more →

Health Canada approves Tevimbra (tislelizumab for injection) in combination with gemcitabine and cisplatin for the first-line treatment of adult patients with recurrent or metastatic nasopharyngeal carcinoma

23 December 2025 - Approval supported by results of the RATIONALE-309 study demonstrating statistically significant improvement in progression-free survival ...

Read more →

FDA approves Omeros’ Yartemlea - first and only therapy indicated for transplant-associated thrombotic microangiopathy

24 December 2025 - Omeros Corporation today announced that the US FDA has approved Yartemlea (narsoplimab-wuug) for the treatment of haematopoietic ...

Read more →

Organogenesis announces initiation of biologics license application for ReNu

23 December 2025 - Initial modules submitted to FDA under rolling review; final modules expected in the first half of ...

Read more →

Millions need New Year medicines price cut

24 December 2025 - New data reveals Australians are still faced with the tough choice of skipping or rationing medicines—due ...

Read more →