Company intelligence / Profile preview
Klinge Biopharma
- Ownership
- Private
- Development stage
- Other
Overview
Klinge Biopharma, through licensing partnerships, commercializes biosimilars in ophthalmologic, immunologic, and other therapy areas. The FDA and EMA approved FYB203 (aflibercept biosimilar/AHZANTIVE®) in 2024-2025 for major retinal indications, and Klinge is the global commercialization rightsholder for this product, with Teva and others handling region-specific launches. The company also sells established brands and generics in Germany.
- Therapeutic areas
- Ophthalmology
- Modalities
- BiologicBiosimilarSmall molecule
- Industry
- Biotech
Drug pipeline
1 assetPartnerships
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