Subcategory & Sub-subcategory
Specifications
- Regulatory Status: Developed from a cell line with DMF filing in place, ensuring global regulatory readiness and streamlined submission for this RSV F-protein inhibitor mAb (originator: AbbVie, first approved 1998-06-19, United States).
- Purity: Demonstrates a high degree of analytical comparability to the reference product, supporting regulatory and clinical acceptance as a biosimilar.
- Expression System: Produced from an optimized, high-titer mammalian cell line and process delivering consistently strong productivity for cost-efficient large-scale manufacturing, with broad media adaptability across multiple platforms.
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