CHDM clinical trials at UCLA

1 research study open to eligible people

DMCRN-02-001: Assessing Pediatric Endpoints in DM1
open to eligible people ages up to 59 months
The overall goal of the study is to establish valid clinical endpoint assessments for children with congenital myotonic dystrophy type 1 and childhood myotonic dystrophy type 1, and develop biomarkers for the condition.
Los Angeles, California and other locations

Last updated: June 2024