Swipe the table sideways for more columns.

TrialConditionsStatusPhaseUpdatedMore infoNCT ID
An Open-Label Extension Study of PGN-EDODM1 in People With Myotonic Dystrophy Type 1 (FREEDOM-OLE)Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Muscular Disorders, Atrophic, hereditary disease, inherited neurodegenerative disorder, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, myotonic dystrophy, myotonic syndrome, nervous system disorder, neurodegenerative disease, neuromuscular diseaseRecruitingPhase 22026-03-30NCT07220603

1 results · Page 1 of 1

Swipe the table sideways for more columns.

OrganizationsLinked trials
PepGen Inc2

3 results · Page 1 of 1

Swipe the table sideways for more columns.

Research sitesCityCountryLinked trials
CIUSSS du Saguenay-Lac-Saint-JeanSaguenayCanada1
Ottawa Hospital Research InstituteOttawaCanada5
University of CalgaryCalgaryCanada31