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RSS FeedPosted by Michael Wonder on 19 Sep 2025
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 ...
Posted by Michael Wonder on 19 Sep 2025
Biocon Biologics' Yesafili (aflibercept) now publicly funded in Ontario, Canada for the advanced treatment of patients with retinal diseases
18 September 2025 - -- Biocon Biologics is pleased to announce that Yesafili (aflibercept), a biosimilar to Eylea (aflibercept) injection, ...
Posted by Michael Wonder on 18 Sep 2025
Minovia Therapeutics receives FDA fast track designation for MNV-201 in myelodysplastic syndrome
18 September 2025 - Minovia Therapeutics announces that the US FDA has granted fast track designation to the Company’s lead investigational ...
Posted by Michael Wonder on 18 Sep 2025
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). ...
Posted by Michael Wonder on 18 Sep 2025
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 ...
Posted by Michael Wonder on 18 Sep 2025
Anti-MTBR (microtubule binding region) tau antibody etalanetug granted FDA fast track designation
16 September 2025 - Eisai announced today that etalanetug (E2814), an investigational anti-MTBR (microtubule binding region) tau antibody, was granted fast ...
Posted by Michael Wonder on 17 Sep 2025
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 ...
Posted by Michael Wonder on 17 Sep 2025
PHARMAC proposes funding a new brand of ADHD medicine
17 September 2025 - PHARMAC is seeking feedback on a proposal to fund a new brand of methylphenidate to help ...
Posted by Michael Wonder on 17 Sep 2025
Besremi gains reimbursement as second-line therapy for polycythemia vera in Korea
27 August 2025 - PharmaEssentia Korea announced on Wednesday that Besremi (ropeginterferon alfa-2b), a treatment for polycythemia vera, will be ...
Posted by Michael Wonder on 17 Sep 2025
FDA grants fast track designation to Corbus Pharmaceuticals’ nectin-4 targeting ADC CRB-701 in head and neck squamous cell carcinoma
16 September 2025 - Corbus Pharmaceuticals announced today that the US FDA has granted fast track designation to CRB-701 for the ...
Posted by Michael Wonder on 17 Sep 2025
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 ...
Posted by Michael Wonder on 16 Sep 2025
AbbVie's Vraylar (cariprazine) now publicly reimbursed in Alberta
15 September 2025 - AbbVie announced today that Alberta has listed Vraylar (cariprazine) on its Health Drug Formulary. ...
Posted by Michael Wonder on 15 Sep 2025
ICER to undertake special report on Crohn’s disease and ulcerative colitis for CMS as part of public comment process on Medicare drug price negotiations
15 September 2025 - Report to reflect legislative specifications in the Inflation Reduction Act and most recent CMS guidance regarding ...
Posted by Michael Wonder on 15 Sep 2025
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 ...
Posted by Michael Wonder on 15 Sep 2025
Raludotatug deruxtecan granted breakthrough therapy designation by US FDA for patients with CDH6 expressing platinum-resistant ovarian, primary peritoneal or fallopian tube cancers previously treated with bevacizumab
15 September 2025 - Raludotatug deruxtecan has been granted breakthrough therapy designation by the US FDA for the treatment of ...