Verona Pharma’s Ohtuvayre (Ensifentrine) Receives the US FDA's Approval to Treat Chronic Obstructive Pulmonary Disease (COPD)
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The US FDA has approved Ohtuvayre as a maintenance therapy to treat COPD patients, with its launch anticipated in Q3’24
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The approval was based on the P-III (ENHANCE-1 & ENHANCE-2) studies analyzing Ohtuvayre monotx. or in addition with other maintenance therapies. Trials reached their 1EPs showing improved lung function; results were published in the American Journal of Respiratory and Critical Care Medicine
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Ohtuvayre is a dual PDE3 & PDE4 inhibitor which possesses both bronchodilator & non-steroidal anti-inflammatory activities. It is administered using a standard jet nebulizer into the lungs
Ref: Verona Pharma | Image: Verona Pharma
Related Post:- Verona Pharma Reports the US FDA Acceptance of NDA for Ensifentrine to Treat Chronic Obstructive Pulmonary Disease
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A passionate content writer with expertise in delivering high-quality and engaging content, Dipanshu is a keen reader and a versatile writer. Dipanshu dedicatedly covers news ranging from biopharma, life sciences, biotech, and MedTech to diagnostics and animal health companies. He can be contacted at connect@pharmashots.com