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GeneCradleAAV viral vector gene therapy drug clinical trial progress in China will soon be presented on the international stage

2024-04-30

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The Global Cell & Gene Therapy Summit 2024 (CGT Summit 2024) will be held in Boston, Massachusetts, USA from July 8 to 10, 2024. Beijing GeneCradle Technology Co., Ltd. (hereinafter referred to as "GeneCradle") will share the progress of the Chinese clinical trials of GeneCradle's independently developed gene therapy drugs GC101 for the treatment of spinal muscular atrophy and GC301 for the treatment of Pompe disease. This sharing is the first time that GeneCradle has actively disclosed the progress of its registered clinical trials on the international stage. This opportunity will promote the exchange between GeneCradle and experts and scholars in the field of gene therapy at home and abroad, accelerate the transformation of scientific discoveries into clinical applications, and lay the foundation for better and earlier benefits to global human health.



Time:July 08-10, 2024 

Venue:Boston, MA, USA

Sessions:Gene Therapy: Methods, Strtegies & Clinical Applications

Poster Presentation Title

Spinal Muscular Atrophy and Pompe Disease Gene Therapy Clinical Trials in China

Presenting Author Xiaodong Wang, Ph.D

Trained in human genetics and serving as the vice president of medical affairs at GeneCradle Therapeutics, Dr. Wang is actively involved in clinical trial protocol designs, data analysis, and results discussion with investigators.

Abstract

Spinal muscular atrophy (SMA) and Pompe disease (PD) are both rare diseases that can be life-threatening or significantly impact the quality of life. GC101 and GC301 are AAV-based gene therapy drugs specifically designed to treat SMA and PD, respectively. Intrathecal administration of GC101 and intravenous administration of GC301 have demonstrated safety and provided clinically significant improvement in  survival, motor function, and achievement of motor milestones, which were not previously expected in  patients with SMA and PD.


ABOUT SUMMIT

Cell and gene therapy represent intersecting fields of biomedical research with the shared goal of treating, preventing, or curing diseases. These approaches are aimed at understanding the underlying causes of various diseases, ranging from rare and complex conditions to those with genetic or acquired origins. This rapidly expanding treatment approach is poised to address significant unmet medical needs across a wide range of conditions. However, the conceptual framework of cell and gene therapy is both expensive and requires precision, presenting challenges for industrial implementation and patient accessibility.

Emerging tools and techniques in the market have facilitated the adaptability and utilization of cell and gene therapy. These advancements have made it easier to employ CGT as a method of treating diseases, including rare and complex disorders, single gene disorders, and various types of cancer. With these advancements in mind, the International Summit on Cell and Gene Therapy serves as a platform to explore the fundamental concepts of these transformative therapies. The summit brings together experts from academia and industry to discuss a range of topics related to cell and gene therapy, including ethical considerations, social implications, tools, techniques, marketing strategies, and the commercialization of cell and gene therapy products. It also showcases the latest research progress in CGT and explores opportunities for further enhancements in availability and productivity of these therapies. By fostering collaboration and knowledge exchange, the summit aims to advance the field of cell and gene therapy, benefiting patients worldwide.

About GeneCradle

Beijing GeneCradle Technology Co., Ltd. is a national high-tech enterprise with the development of gene therapy drugs mediated by AAV vector delivery technology as its core business. Its mission is to promote China's rare disease gene drugs from basic to clinical and market, benefiting patients and families. The company focuses on the development of gene therapy drugs in the fields of hereditary neuromuscular diseases, genetic metabolic diseases, lysosomal diseases and ophthalmic diseases. By promoting the development and clinical application of rare disease gene drugs, it has a deeper understanding of life and health, and has transitioned gene therapy technologies and products from rare diseases to the treatment and rehabilitation of chronic diseases and other major diseases.