XL-protein Grants Worldwide License to Grifols to Develop a Biopharmaceutical Using PASylation® Technology

XL-protein GmbH has entered into a worldwide License, Development and Commercialization Agreement with Grifols, for a novel, long-acting biopharmaceutical product.

Under this collaboration, XL-protein will leverage its proprietary, clinical-stage PASylation® technology to extend the circulation of Grifols therapeutics, paving the way for a more effective and long-lasting treatment. XL-protein will actively support preclinical development activities while Grifols will be entitled to further developing as well as manufacturing and marketing the PASylated-enhanced biologic.

Under the terms of the agreement, XL-protein will receive an upfront payment as well as payments for achievement of preclinical, clinical, regulatory and commercial milestones. Furthermore, XL-protein will receive tiered royalties on sales from marketed therapeutics resulting from the collaboration. Grifols will have worldwide exclusive marketing rights under the agreement. Further financial terms have not been disclosed.

”Grifols continues to innovate across its therapeutic portfolio to develop new treatments and enhancing existing ones for patients”, said Dr. Jörg Schüttrumpf, Grifols Chief Scientific Innovation Officer. “We look forward to collaborating with XL-protein and combining our advanced scientific efforts in this leading initiative”.

"We are excited to work with Grifols to enhance the pharmacological properties of their therapeutics", said Dr. Michaela Gebauer, Managing Director of XL-protein. "This partnership leverages the potential of our PASylation technology, together with other PASylated drugs currently under development, and creates added value for Grifols", commented Uli Binder, Managing Director of XL-protein.

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