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CANbridge to Acquire Gene Therapy for Rare Diseases from Scriptr

publication date: Oct 25, 2021

CANbridge, a Beijing rare disease-focused biopharma, entered a research collaboration and license agreement with Scriptr Global to develop a gene therapy for dystrophinopathies. Scriptr is a preclinical Cambridge MA company that develops therapies for dystrophinopathies based on its proprietary ribozyme-mediated RNA assembly technology, CANbridge will gain exclusive global rights to a gene therapy candidate that uses Scriptr’s Stitchr™ platform and is aimed at X-linked genetic muscular diseases, which include several rare childhood diseases. More details....

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