Tolebrutinib regulatory submission accepted for priority review in the US for patients with multiple sclerosis

25 March 2025 - Tolebrutinib was granted breakthrough therapy designation by the FDA based on positive results from the HERCULES Phase ...

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Government of Canada signs bilateral agreement with Quebec for Drugs for Rare Diseases

21 March 2025 - In Canada, one in 12 people live with a rare disease, and for most people affected, the ...

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Sungen Biomedical's world first new drug SGC001 monoclonal antibody receives FDA fast track approval

24 March 2025 - On 17 March 2025, US time, the world's first acute myocardial infarction antibody drug, SGC001, developed by ...

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GSK’s application to expand use of Nucala (mepolizumab) for the treatment of COPD accepted for review by the European Medicines Agency

24 March 2025 - Submission based on data from MATINEE trial, which showed a statistically significant and clinically meaningful reduction in ...

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CStone submits application to the EMA for new indication of sugemalimab in stage III non-small cell lung cancer

23 March 2025 - CStone Pharmaceuticals today announced the submission of a type II variation application to the EMA for sugemalimab.  ...

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Public Summary Documents (first time rejections and deferrals)– November 2024 PBAC meeting

21 March 2025 - The Public Summary Documents (first time decisions not to recommend and deferrals) from the November 2024 PBAC ...

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Strengthening Medicare: cheaper medicines to get even cheaper

20 March 2025 - The Albanese Labor Government is making cheaper medicines even cheaper – with a script to cost ...

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Novartis receives third FDA approval for oral Fabhalta (iptacopan) – the first and only treatment approved in C3 glomerulopathy

20 March 2025 - Phase 3 study showed sustained proteinuria reduction at one year with favourable safety. ...

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Hikma announces Health Canada approval of Kloxxado (naloxone hydrochloride) nasal spray 8 mg

20 March 2025 - Emergent BioSolutions will lead commercial launch efforts to increase access to intranasal naloxone and combat opioid overdose ...

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US FDA approves Tremfya (guselkumab), the first and only IL-23 inhibitor offering both subcutaneous and intravenous induction options, for adult patients with moderately to severely active Crohn’s disease

20 March 2025 - Supported by data from the GALAXI study, Tremfya is the only IL-23 inhibitor to show superiority versus ...

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Why US drug giants are so angry about Australia’s PBS

20 March 2025 - US pharmaceutical giants hope the protectionist Trump administration will force Australia to increase the price it pays ...

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Health Economics Methods Advisory Group selects first area for study: assessing treatment benefits appropriate to consider in HTA decision-making

18 March 2025 -  The US based ICER, England’s NICE and Canada’s Drug Agency have selected the first research topic ...

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FDA approves pembrolizumab for HER2 positive gastric or gastro-oesophageal junction adenocarcinoma expressing PD-L1

19 March 2025 - Today, the FDA granted traditional approval to pembrolizumab (Keytruda, Merck) with trastuzumab, fluoropyrimidine- and platinum-containing chemotherapy ...

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Health Canada approves Keytruda for the treatment of adult patients with primary advanced or recurrent endometrial carcinoma, in combination with carboplatin and paclitaxel and then continued as monotherapy

19 March 2025 - Approval is based on the Phase 3 KEYNOTE-868/NRG-GY018 trial. ...

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PBS medication to cost no more than $25 under Labor re-election pitch

19 March 2025 - Australians are set to save a combined $200 million a year under the plan, which will cost ...

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