Fresenius Kabi SwissBioSim GmbH
Quick facts
Phase 3 pipeline
- EU-approved RoActemra · Immunology
RoActemra (tocilizumab) is a humanized monoclonal antibody that blocks the interleukin-6 (IL-6) receptor, reducing inflammatory signaling in immune-mediated diseases. - EU-Humira
- FKS518 · Immunology
FKS518 is a calcineurin inhibitor that suppresses T-cell activation by blocking the phosphatase calcineurin, thereby reducing immune-mediated rejection. - MSB11022 · Oncology
MSB11022 is a biosimilar of trastuzumab that targets HER2-positive cancer cells by binding to the HER2 receptor and inhibiting tumor growth. - MSB11456 · Oncology
MSB11456 is a biosimilar of trastuzumab that targets HER2-positive cancer cells by binding to the HER2 receptor and blocking growth signaling. - US-licensed Prolia (Amgen) · Osteoporosis
Prolia is a human monoclonal antibody that targets RANKL, a protein involved in bone resorption.
Phase 1 pipeline
Competitive intelligence
For the full portfolio CI brief — phase mix, recent regulatory actions, upcoming PDUFA dates, patent timeline, class-overlap with competitors:
- Fresenius Kabi SwissBioSim GmbH portfolio CI brief
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Frequently asked questions about Fresenius Kabi SwissBioSim GmbH
What is Fresenius Kabi SwissBioSim GmbH's pipeline?
Fresenius Kabi SwissBioSim GmbH has 6 drugs in Phase 3, 0 in Phase 2, 2 in Phase 1. Late-stage candidates include EU-approved RoActemra, EU-Humira, FKS518, MSB11022.
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