November 17, 2025 – Polpharma Biologics, a biopharmaceutical company group focused on biosimilars development and manufacturing, today confirmed that Sandoz Tyruko® (natalizumab-sztn) is now available to patients in the United States. Tyruko® is the first and only FDA-approved biosimilar of natalizumab for the treatment of relapsing forms of multiple sclerosis (MS), and also for adult patients with...

Zurich, Switzerland – October 21, 2025 – Polpharma Biologics today announced Ranivisio® PFS (ranibizumab biosimilar pre-filled syringe), is now commercially available in France. Ranivisio® is the first Lucentis® biosimilar which is offered in a convenient pre-filled syringe (PFS) presentation in Europe, setting a new standard for affordable biologics in ophthalmic care. This innovative configuration...

Polpharma Biologics is splitting its operations into two independent companies, each with a clear focus and mission.We will operate our biosimilars business out of Switzerland, under the original brand – Polpharma Biologics. We remain dedicated to developing and commercializing our pipeline of high-quality biologic medicines. We chose Switzerland, a strong biotech hub, for its proximity to our business...

Amsterdam, Gdańsk – September 2nd, 2025 – Polpharma Biologics S.A. (“Polpharma Biologics”), specialized in the development and manufacturing of biosimilars, today announced that it has signed licensing agreements with MS Pharma, a leading biosimilar production and distribution company in the Middle East and North Africa (MENA) region, for the commercialization of its biosimilar candidates vedolizumab...

Amsterdam, Gdańsk – August 5, 2025 – Polpharma Biologics S.A. (“Polpharma Biologics”) announces a global (except for Middle East & North Africa) licensing agreement with Fresenius Kabi for the commercialization of PB016, a proposed biosimilar to vedolizumab, an integrin receptor antagonist, (reference product: Entyvio®*), a biologic therapy indicated for moderate to severe ulcerative colitis and...

Amsterdam, Munich – Polpharma Biologics Group BV (“Polpharma Biologics”) and Bioeq AG (“Bioeq”) jointly announce that the Brazilian Health Regulatory Agency (ANVISA) has approved Ranivisio®* (ranibizumab) as a biosimilar to Lucentis®** for the treatment of debilitating retinopathies in Brazil.1 Ranivisio®, developed by Bioeq (a Joint Venture between Polpharma Biologics and Formycon AG) will be exclusively...

In October, together with the Warsaw University of Life Sciences [SGGW], we are launching the new Polpharma Biologics...

Polpharma Biologics at IMPACT CEE

CEBioForum 2024 is an annual international conference for the biotechnology sector and also the largest industry even...

We are expanding our research portfolio - that's what you'll read about in Puls Biznesu. Editor Marcel Zatoński spoke...