drugset / Trial / NCT07119775
Tideglusib: Expanded Access Use in Congenital Myotonic Dystrophy
Summary
This treatment plan is limited to a single patient with Congenital Myotonic Dystrophy, who is ineligible or otherwise unable to participate in ongoing clinical trials.
Timeline
- Start
- —
- Primary completion
- —
- Completion
- —
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Tideglusib | Small molecule | — | — |