Polpharma Biologics
About Polpharma Biologics
Certifications
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FDA -
GMP
Categories
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Country/Region:Poland
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On CPHI since:2021
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Certificates:3
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Employees:50 - 99
Company types
Primary activities
Contact info
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Trzy Lipy 3 Building A, Gdansk Science & Technology Park, 80-172, Gdansk, Poland
Meet us at
CPHI Milan 2026
Fiera Milano, Italy
6 Oct 2026 - 8 Oct 2026
Products from Polpharma Biologics (1)
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Product Pipeline
With approved biosimilars already on the market and a robust pipeline of differentiated assets,Polpharma Biologics is well-positioned to shape the future of biosimilars. Strategic collaborationswith industry leaders demonstrate the company’s ability to co-create value and deliver at scale.
Polpharma Biologics Resources (5)
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News Polpharma Biologics’ investigational biosimilar shows PK/PD comparability to inflammatory bowel disease blockbuster Entyvio®
Polpharma Biologics, announced topline results demonstrating the pharmacokinetic (PK) and pharmacodynamic (PD) comparability of its biosimilar candidate PB016 to its reference drug, Entyvio®* (vedolizumab).
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News Polpharma Biologics announces approval of Europe’s first and only biosimilar for multiple sclerosis - Tyruko® (natalizumab)
Polpharma Biologics announced that the European Commission (EC) has approved Tyruko® (natalizumab) as the first and only biosimilar for relapsing forms of multiple sclerosis (MS) in Europe. Tyruko® was developed by Polpharma Biologics and will be commercialized by its collaboration partner Sandoz.
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Datasheet Pipeline
With approved biosimilars already on the market and a robust pipeline of differentiated assets,Polpharma Biologics is well-positioned to shape the future of biosimilars. Strategic collaborationswith industry leaders demonstrate the company’s ability to co-create value and deliver at scale. -
News Polpharma Biologics announces FDA approval of Tyruko®
Polpharma Biologics, announced that the FDA is the first regulatory body worldwide to approve the use of Tyruko® (natalizumab-sztn) - a new biosimilar for the treatment of relapsing forms of multiple sclerosis (MS). Approval of Tyruko® by the European Medicines Agency is also expected imminently.
