FDA Approves EBGLYSS™ for Adults and Children with Atopic Dermatitis
FDA Grants Approval for New Atopic Dermatitis Treatment
Eli Lilly and Company (NYSE: LLY) announced today that the U.S. Food and Drug Administration (FDA) has approved EBGLYSS™ (lebrikizumab-lbkz), an innovative treatment aimed at adults and children aged 12 years and older with moderate-to-severe atopic dermatitis.
Significance of EBGLYSS™ Approval
This groundbreaking therapy acts as a targeted IL-13 inhibitor, addressing a key factor in the inflammatory process associated with atopic dermatitis. The approval signifies a new horizon in managing a condition that affects millions and often leads to substantial discomfort and impairment in quality of life.
About Atopic Dermatitis
- Commonly referred to as eczema, atopic dermatitis is a chronic skin condition characterized by dry, itchy skin.
- The condition can significantly impact individuals’ daily activities and emotional well-being.
- Current treatments have often focused on managing symptoms rather than targeting the underlying causes.
With the introduction of EBGLYSS™, patients and healthcare providers now have a more effective option for targeted treatment.
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