MICRO-DYSTROPHIN - Systemic Gene Delivery Clinical Trial for Duchenne

 

Frequently Asked Questions (FAQs) about this study:

 

What stage is this research?

  • This phase I/2a clinical trial is actively recruiting participants.    

 

What is the goal or purpose of this study?

  • The goal of this study is evaluate safety and efficacy in 12 boys with Duchenne following a single infusion of rAAVrh74.MHCK7.micro-dystrophin.

 

Who is funding this study?

  • This study is sponsored by Nationwide Children's Hospital.

 

Who is eligible to participate in this study?

  • To participate in this study you must be a boy with Duchenne, between 3 months and 7 years of age, ambulatory, and have a DMD Glossary Link gene Glossary Link mutation between exons 18-58.  For a complete list of all the inclusion and exclusion criteria, please visit ClinicalTrials.gov.

 

What do I have to do if I decide to participate in this study?

  • This study involves a single infusion in the arm of the rAAVrh74.MHCK7.micro-dystrophin.  This will take place at Nationwide Children's Hospital.  There will be close follow-up for 2 years, including several muscle biopsies, laboratory tests, and physical exams. 

 

Where does this study take place?

  • This study takes place at Nationwide Children’s Hospital in Columbus, Ohio, and Washington University School of Medicine in St. Louis, MO. 

 

Where can I learn more about this study?

  • You can learn more about this study at www.ClinicalTrials.org (NCT03375164). You can also contact the study coordinator Alana Mahley at This email address is being protected from spambots. You need JavaScript enabled to view it. or 614-355-2606.

 

(Updated 12/18/17)