CANbridge Pharmaceuticals Announces CAN008 Phase 1/2 Glioblastoma Multiforme Abstract Accepted by the ESMO Sarcoma and Rare Cancers Congress
Beijing, China; Burlington, Mass., March 13, 2023 — CANbridge Pharmaceuticals, Inc. (1228.HK), a global biopharmaceutical company, with a foundation in China, committed to the research, development and commercialization of transformative therapies to treat rare diseases and oncology, announced that an abstract on the long-term follow up data from the CAN008 Phase 1/2 trial in glioblastoma multiforme has been accepted for a poster presentation by the European Society for Medical Oncology (ESMO) Sarcoma and Rare Cancers Annual Congress, taking place March 20-22, in Lugano, Switzerland.
Title: “Long term follow-up to the phase I/II study of CAN008 plus
standard chemoradiotherapy treatment in patients with newly diagnosed glioblastoma multiforme”
Authors: Ian Yi-Feng Chang, PhD, Hong-Chieh Tsai, MD, PhD, Chia-Hua Chen, PhD., Hsiu-Chi Chen, MSc, Chia-Wen Huang, MSc, Gerald. F. Cox, MD, PhD, Fang-Min Huang, MD, You-Yu Lin, PhD, Ko-Ting Chen, MD, PhD, Ya-Jui Lin, MD, PhD, Kuo-Chen Wei, MD
Poster Session: March 20-22
About CANbridge Pharmaceuticals Inc.
CANbridge Pharmaceuticals Inc. (HKEX:1228) global biopharmaceutical company, with a foundation in China, committed to the research, development and commercialization of transformative therapies for rare disease and rare oncology. CANbridge has a differentiated drug portfolio, with three approved drugs and a pipeline of 10 assets, targeting prevalent rare disease and rare oncology indications that have unmet needs and significant market potential. These include Hunter syndrome and other lysosomal storage disorders, complement-mediated disorders, hemophilia A, metabolic disorders, rare cholestatic liver diseases and neuromuscular diseases, as well as glioblastoma multiforme. The CANbridge Next-Generation Innovation and Process Development Facility is developing novel, potentially curative, gene therapies for rare genetic diseases, including Pompe disease, Fabry disease, spinal muscular atrophy (SMA) and other neuromuscular conditions, and collaborates with world-leading researchers and biotech companies. Animal data from the SMA gene therapy was presented in 2022 at the American Society for Gene and Cell Therapy (ASGCT), the European Society for Gene and Cell Therapy (ESGCT) and the World Muscle Congress. CANbridge global partners include: Apogenix, GC Pharma, Mirum, Wuxi Biologics, Privus, UMass Chan Medical School, the University of Washington School of Medicine and Scriptr Global.
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