Shots:
The Ghana FDA has approved BioUcenta, a biosimilar version of Lucentis (ranibizumab) for diabetic macular edema, age-related macular degeneration, and diabetic retinopathyÂ
The Ghana FDA approval followed a rigorous, science-based review referencing comprehensive data previously evaluated and accepted by the EMAÂ
BioUcenta is exclusively licensed to Bio Usawa for Sub-Saharan Africa by Bioeq AGÂ
Ref: Bio Usawa | Image: Bio Usawa |  Press ReleaseÂ
Related News: CuraTeQ Biologics Reports Positive P-III study…
Shots:
Bio Usawa Biotechnology and Bioeq AG entered into an agreement to make ranibizumab biosimilar for serious retinal diseases, accessible to millions in Sub-Saharan Africa Â
The partnership gives Bio Usawa exclusive rights to register and market Bioeq’s ranibizumab biosimilar, BioUcenta, advancing access to essential biologics in Sub-Saharan Africa Â
BioUcenta, an intravitreal injection, blocks abnormal retinal…
Biosimilars are developed to be highly similar versions of approved biologics in terms of safety, purity, and potency
Biosimilars are expected to be a cost-effective alternative to the high-priced branded biologics, offering significant and much-needed cost savings to both payers and the patients
During the month of June, Organon entered into an agreement with Henlius…

