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0 0.00197903294822424 0.0010697475395806 0.000481386392811315 -0.00470688917415488 -0.00861146769362423 -0.00438596491228067 -0.000748823277706388
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BREZTRI approved in the US for asthma as first and only triple therapy for patients 12 years of age and older

AstraZeneca PLC Ordinary Shares (AZN) 
Last astrazeneca plc ordinary shares earnings: 2/5 04:00 pm Check Earnings Report
US:NYSE Investor Relations: astrazeneca.com/investor-relations.html
Company Research Source: Business Wire
Approval based on KALOS and LOGOS Phase III trials demonstrating statistically significant and clinically meaningful benefits of AstraZeneca’s single-inhaler fixed-dose triple therapy compared with inhaled dual therapyApproval is second indication for BREZTRI beyond COPD WILMINGTON, Del.--(BUSINESS WIRE)--AstraZeneca’s fixed-dose triple-combination therapy BREZTRI Aerosphere® (budesonide/glycopyrrolate/formoterol fumarate or BGF 320/36/9.6µg) has been approved in the US for the maintenance treatment of asthma in adult and pediatric patients 12 years of age and older. BREZTRI is a single-inhaler that combines the efficacy of corticosteroid/long-acting beta2-agonist (ICS/LABA) medicines with a long-acting muscarinic antagonist (LAMA). BREZTRI (320/18/9.6µg) was approved in the US in 2020 to treat adults with chronic obstructive pulmonary disease (COPD) and was prescribed to more than 6.8 million patients globally in 2025.1,2The approval by the US Food and Drug Administration (FDA) wa Show less Read more
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