Biocon Biologics receives Health Canada approval for Yesafili
The approval is based on a comprehensive package of analytical, nonclinical, and clinical data
The approval is based on a comprehensive package of analytical, nonclinical, and clinical data
EBITDA before special items decreases to €4.08 billion (7.4%)
YESAFILI, a vascular endothelial growth factor (VEGF) inhibitor, is used to treat several different types of ophthalmology conditions
Regulatory filings underway for a third indication for darolutamide in prostate cancer, for finerenone in a common form of heart failure, and acoramidis in transthyretin amyloid
Demonstrates vision gains with extended treatment intervals in retinal vein occlusion
Pharmaceuticals and Consumer Health report higher sales (Fx & portfolio adj.) and lower earnings
The approval of YESAFILI marks Biocon Biologics’ expansion into the ophthalmology therapeutic area in the United States
This agreement paves the way for the introduction of YESAFILI into the Canadian market
Yesafili, received marketing authorization approval from the European Commission for the European Union
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