TECPR2 Research Foundation and Forge Biologics Partner to Advance Gene Therapy for Ultra-Rare Disease
The TECPR2 Research Foundation, a non-profit dedicated to finding treatments for TECPR2, has announced a development and manufacturing partnership with Forge Biologics, a gene therapy manufacturer. This collaboration aims to advance an AAV gene therapy for patients suffering from TECPR2, an ultra-rare neurodegenerative genetic disease. Under the agreement, Forge Biologics will provide process development, analytical development and qualification, and manufacturing services, including the production and release of materials for toxicology studies. The program will utilize Forge’s proprietary FUEL™ platform, which includes HEK293 suspension Ignition Cells™ and pEMBR™ 2.0 adenovirus helper plasmid, designed to enhance manufacturing efficiencies. The investigational gene therapy seeks to deliver a functional copy of the TECPR2 gene using an AAV vector, addressing the underlying genetic cause of the disease. Research for this program is led by Steven Gray, Ph.D., and Xin Chen, M.D., Ph.D., at UT Southwestern Me...