Biopharmaceutical company AstraZeneca (LSE: AZN) (STO: AZN) (NYSE: AZN) declared on Wednesday that it has received European Commission approval for Trixeo Aerosphere as a maintenance treatment for asthma in patients aged 12 and over who are inadequately controlled on medium-dose inhaled corticosteroid and long-acting beta2-agonist therapy. Trixeo is the first triple-combination therapy approved in the EU for this population regardless of exacerbation history.
This approval follows a positive opinion from the European Medicines Agency's Committee for Medicinal Products for Human Use and was supported by Phase III KALOS and LOGOS trials. Trixeo demonstrated statistically significant improvements in lung function and, in pooled analysis, a significant reduction in the annualised rate of severe asthma exacerbations versus dual therapy.
The trials involved approximately 4,300 patients and identified no new safety or tolerability signals. Trixeo is marketed as Breztri Aerosphere in the US, China and Japan and is also approved for asthma in the US and Japan, while regulatory reviews are ongoing in other markets.
Trixeo Aerosphere is also approved for chronic obstructive pulmonary disease in more than 90 countries and was prescribed to more than 6.8 million patients globally in 2025.
PureTech receives FDA Fast Track designation for LYT-200 in HR-MDS
MaaT Pharma outlines potential Phase 3 development plan for MaaT013 after CHMP negative opinion
Bayer's Kerendia wins FDA approval for chronic kidney disease associated with type 1 diabetes
Myosin Therapeutics chosen for 2026-2027 NCI Investor Initiatives Showcase
Medtronic receives FDA clearance for LigaSure RAS Maryland instrument on Hugo system
VaxThera partners with Codagenix for next generation yellow fever vaccine advancement
MaaT Pharma receives negative CHMP trend vote for MaaT013
FDA approves Scholar Rock's ISEMBYLD to treat spinal muscular atrophy
FDA grants priority review to Takeda's zasocitinib application for plaque psoriasis
Armata Pharmaceuticals announces receipt of FDA Breakthrough Therapy Designation for AP-SA02
GSK reports positive Jideytro data supporting potential first-line lung cancer use
Eloxx Pharmaceuticals commences Phase 2b study of exaluren
Meant Health announces expansion of telehealth access for FDA-approved GLP-1 prescriptions
US FDA grants orphan drug designation for Lundbeck's asedebart