WiTNNess - TNNT1 Myopathy Natural History Study
WiTNNess - TNNT1 Myopathy Natural History Study
Recruiting · NCT06374719 · Registry updated 2026-06-23Clinical trials
Swipe the table sideways for more columns.
| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| WiTNNess - TNNT1 Myopathy Natural History Study | congenital structural myopathy, hereditary skeletal muscle disorder, muscle tissue disorder, musculoskeletal system disorder, nemaline myopathy, nemaline myopathy 5, nervous system disorder, neuromuscular disease | Recruiting | Not stated | 2026-06-23 | NCT06374719 |
1 results · Page 1 of 1
Organizations
Swipe the table sideways for more columns.
| Organizations | Linked trials |
|---|---|
| Clinic for Special Children | 1 |
1 results · Page 1 of 1
Research sites
Swipe the table sideways for more columns.
| Research sites | City | Country | Linked trials |
|---|---|---|---|
| Clinic for Special Children | Gordonville | United States | 2 |