Teva and mAbxience expand partnership for additional oncology biosimilar candidate
10/25/24, 3:30 PM
Location
Industry
biotechnology
Type
partnership
Teva and mAbxience have announced a new global licensing agreement for the development of an anti PD-1 oncology biosimilar candidate. mAbxience will lead the development and production of the biosimilar, utilizing its state-of-the-art, cGMP-compliant facilities in Spain and Argentina, while Teva will manage regulatory approvals and oversee commercialization in the designated markets. This collaboration further strengthens the alliance between Teva and mAbxience, aiming to provide cost-effective, high-quality biosimilar treatments for critical unmet needs in oncology care.
Company Info
Location
madrid, community of madrid, spain
Additional Info
mAbxience is a Spanish-based company specializing in the development, production, and commercialization of biopharmaceuticals. With over a decade of expertise, our mission is clear: to provide accessible, affordable medicines across the globe, aiming to enhance the quality of life by ensuring universal access to high-caliber medicines. With two market-approved products and a robust pipeline in development, we have established a B2B presence in over 100 markets. Alongside this, we have formed a network with more than 30 partners and built a dedicated team of over 1,000 professionals. Our three multi-product facilities, located in Europe and South America, have obtained GMP approval from esteemed regulatory bodies, including the FDA, EMA, and others. Furthermore, as a global biopharmaceutical expert, mAbxience specializes in Contract Development and Manufacturing Organization services (CDMO), utilizing advanced technology and innovative platforms to deliver integrated manufacturing solutions. For more insights into mAbxience, our biosimilars and CDMO business, please visit our website (www.mabxience.com)
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