News | February 19, 2026
Zydus introduces ANYRA (Aflibercept 2 mg) for advanced retinal disease treatment
ANYRA is India’s first indigenously developed Aflibercept 2 mg biosimilar
ANYRA is India’s first indigenously developed Aflibercept 2 mg biosimilar
All pending litigation between Biocon Biologics, Regeneron, and Bayer will be dismissed
Demonstrates vision gains with extended treatment intervals in retinal vein occlusion
The approval of YESAFILI marks Biocon Biologics’ expansion into the ophthalmology therapeutic area in the United States
Yesafili, received marketing authorization approval from the European Commission for the European Union
The centralized marketing authorization granted by the EC is valid in all EU Member States as well as in the European Economic Area (EEA) countries Iceland, Liechtenstein and Norway
Aflibercept is the second biosimilar product that has entered the clinical trial phase after biosimilar Adalimumab
It promises fewer injections for vision loss patients
Treatment typically requires frequent injections directly into the eye—an ongoing burden for patients and health systems alike
Under the agreement, AVT06 is licensed to enter the US market in the fourth quarter of 2026
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