Webinar: Cell Therapies for Parkinson’s Disease from Discovery to Clinic
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CIRM / Regenerative Medicine Consortium (RMC)
Cell Therapies for Parkinson’s Disease from Discovery to Clinic
Presentations from FDA and Leading Experts
A Webinar was held on November 14th, 2013
Webinar Presentation Links
- Watch recording of webinar
- Download speakers’ slide presentations
- Wilson Bryan slides [pdf]
- Jeffrey Kordower slides [pdf]
- Sheryl Osborne slides [pdf]
- Download printed summary of the Q&A session here
WEBINAR AGENDA & TOPICS
Moderator:
- Ellen Feigal, MD, Senior Vice President of Research and Development, CIRM
Expert Speakers:
- Wilson Bryan, M.D., Director, Division of Clinical Evaluation and Pharmacology/Toxicology (DCEPT), Office of Cellular, Tissue and Gene Therapies (OCTGT), Center for Biologics Evaluation and Research (CBER), U.S. Food and Drug Administration (FDA)
- Jeffrey Kordower, Ph.D., Professor of Neurological Sciences and Neurology, Rush University Medical Center
- Sheryl Osborne, Consultant in Regulatory Affairs and Clinical Development
Topics that were covered:
The focus of this webinar was on Parkinson’s Disease – using the Lessons Learned to overcome the challenges as cell based therapies move from discovery to the clinic.
- Presentation by FDA – Considerations for first-in-human clinical trials of cell therapies for Parkinson’s Disease
- Lessons learned from human fetal transplants and from gene therapy
- State of preclinical research with hESCs and hiPSC cell therapies
- Questions and Answers
Resources:
- CIRM Parkinson’s Disease Workshop White Paper Report [pdf]
- CIRM’s Parkinson’s Disease Fact Sheet
- Podcast: Whatever Happened to Stem Cells? The Michael J. Fox Foundation
Date Published: October 18, 2013
Last Modified: June 28, 2022
Last Modified: June 28, 2022