PB018 (ocrelizumab biosimilar) / Polpharma, MS Pharma, Teva - LARVOL DELTA

Teva and Polpharma Biologics Announce Global Licensing Agreement for a Biosimilar Candidate to Ocrevus (ocrelizumab) for Multiple Sclerosis (GlobeNewswire) - "Under the terms of the agreement, Polpharma Biologics retains full responsibility for the development and manufacturing of the biosimilar candidate. Teva will be responsible for regulatory submissions and, upon approval, commercialization of the intravenous and subcutaneous formulations in the United States, Europe, Brazil, Canada, Australia, New Zealand, Israel and Turkey."

Licensing / partnership • Multiple Sclerosis

Polpharma Biologics S.A…announced that it has signed licensing agreements with MS Pharma…for the commercialization of its biosimilar candidates vedolizumab (PB016), ocrelizumab (PB018) and guselkumab (PB019) in the MENA region. (Businesswire) - "Under the agreements, MS Pharma will be responsible for the registration, marketing, and distribution of these three biosimilars across MENA, while Polpharma Biologics will maintain responsibility for development, manufacturing, and supply. Furthermore, both Parties have agreed to transfer fill and finish activities to the MENA region."

Commercial • Psoriasis • Psoriatic Arthritis • Ulcerative Colitis