ASC Therapeutics is a division of Applied StemCell, Inc. with decades of experience in developing and improving gene editing and stem cell technologies. We are a flock of dedicated scientists, with strong belief in gene and cell therapy, the future for treating intractable diseases.
Co-founder, President and CEO
-20+ years industrial experience (US and China) in research tool, molecular diagnostic product and drug development, and corporate development
-General manager of MicuRx, China
-Founding members of two biotech companies
-Co-founder of two biotech companies
Chief Medical Officer
-20+ years pre-clinical, clinical & regulatory experience
-Responsible for Humira clinical development
-Inventor-2007 US Patent
-100+ peer-reviewed publications
Chief Financial Officer
-20+ years in domestic & international financial transactions
-Closed 11 business development deals (e.g. GSK, Amgen, J&J), up to $600M deal size each transaction
-Closed 11 equity transactions in US ad EU markets
VP, Gene & Cell Therapy
-20 years of biotech experience developing novel technologies and genetic therapies
-Former associate director at Sangamo Therapeutics
-Inventor of multiple patents in the field of gene therapy, gene regulation and genome editing
-Ph.D. in molecular genetics from Washington University
VP, Therapeutic Development
-Over 20 years of executive-level leadership experience, advancing cell, gene and protein therapies from idea through pre-clinical and clinical development in multiple therapeutic areas (Hematology, Immunology, Oncology, Neurology, Dermatology, and Cardiovascular Diseases).
-Former Senior Director of Development and Head of Immuno-Oncology at Neumedicines Inc., Pasadena, CA.
-Former Chief Technology Officer at Gene Grafts Ltd. and Angiogenesis Project Lead at MGVS Ltd., Haifa, Israel.
-Cell and Gene Therapy Consultant and Biforum, Israel.
-PhD in Cell and Molecular Biology and MBA from the Technion, Israel Institute of Technology, Haifa, Israel.
-Co-author of multiple patents and peer-reviewed publications.
VICE PRESIDENT, GLOBAL REGULATORY AFFAIRS
– 20+ years of experience in biomedical research and regulatory affairs (US, EU, Canada, China)
– Broad regulatory experience supporting development and commercialization of biologics, drugs, molecular diagnostics and medical devices
– Successfully submitted several INDs/CTAs for new biologics and drugs
Director, CMC Cell and Gene therapy
-More than 25 years’ experience in research and therapeutics development.
-Proven success in setting up translational medicine platform to bring research into clinic.
-Extensive experience in research, preclinical study, process development, GMP manufacturing, analytical development, and quality control.
-10+ years industrial experience in drug development for gene and cell therapy including autologous and allogeneic CarT and Hematopoietic Stem Cell engineering with lentiviral vector, AAV vector, adenoviral vector, and Zinc Finger Nuclease.