Clin2
NCT07119775Possibly a fitAvailable

Tideglusib for congenital myotonic dystrophy

Congenital Myotonic Dystrophy

Treatments studied

Part of Bones, joints & muscles, Brain & nervous system, Genetic & congenital clinical trials.

This trial provides access to a medication called tideglusib for people with congenital myotonic dystrophy. The goal is to see if it helps with symptoms.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Ages
Any age
Study type
Expanded Access

Who can take part

  • You must have a diagnosis of congenital myotonic dystrophy.
  • You must be able to travel to a participating study site.
  • You must be willing to follow the study's rules and procedures.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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