Santhera Signs a Pre-Clinical Research Agreement with Biozentrum to Advance Gene Therapy for Congenital Muscular Dystrophy
Shots:
- Santhera enters into a collaboration with Biozentrum- University of Basel to explore the feasibility of the gene therapy by standard viral vectors for LAMA2 MD or MDC1A- co-financed by Innosuisse of ~$1.19M
- The focus of the collaboration is to foster Santhera’s neuromuscular pipeline and to utilize Biozentrum’s gene therapy in its Omigapil for improving its benefits in LAMA2 deficient MD
- Biozentrum’s gene therapy utilizes two linker proteins derived from agrin- laminin and nidogen leading to a restoration of muscle fiber- recovery of muscle force and size and increases body weight. Omigapil is a deprenyl-analog- exclusively licensed from Novartis by Santhera for CMD
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