Resources
Information and support are available for families affected by Canavan disease from advocacy organizations such as:
Families can also access resources on gene therapy, drug development and understanding clinical trials by visiting:
Information for Families:
CANinform Family Brochure
CANaspire Family Brochure
NTSAD Family Conference
April 23, 2021
Natural History Webinar
NTSAD Family Conference
April 23, 2021
Aspa Gene Therapy Webinar
Aspa Webinar for Families
September 16, 2020
Introduction to Gene Therapy
Webinar: Aspa’s Approach to Gene Therapy
February 2, 2022
A Closer Look at the Science
Scientific Presentations and Posters:
Aspa is committed to increasing awareness and education about Canavan disease.
Presentations
American Society of Gene & Cell Therapy
May 13, 2021
Evaluation of AAV Gene Therapy for Canavan Disease in Animal Models
EveryLife Foundation Annual Scientific Workshop
September 5, 2019
Building a Natural History Study for Canavan Disease
Washington, D.C.
Posters
The Joint 16th ICNA Congress & 49th Annual CNS Meeting
CANinform Natural History Study Design and COVID-19 Mitigation
October 12-23, 2020
48th Annual Meeting of the Child Neurology Society
Natural History Study Design
October 23-26, 2019
Charlotte, NC
European Society for Gene & Cell Therapy
IV administration compared to IT and ICV
October 22-25, 2019
Barcelona, Spain
Congress for Pediatrics and Adolescent Medicine, focused on pediatric neurology
Natural History Study Design
September 11-14, 2019
Munich, Germany
For additional presentations, posters and publications, please visit www.aspatx.com
Contact
For specific questions related to Aspa’s clinical program, please email: clinicaltrials@aspatx.com
