Swipe the table sideways for more columns.

TrialConditionsStatusPhaseUpdatedMore infoNCT ID
GMEB-SASS: A Gene-Modified Skin Substitute for RDEB TreatmentCollagen Diseases, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hallopeau-Siemens Disease, Skin Abnormalities, Skin and Connective Tissue Diseases, connective tissue disorder, epidermolysis bullosa, epidermolysis bullosa dystrophica, hereditary disease, hereditary skin disorder, recessive dystrophic epidermolysis bullosa, skin disorder, vesiculobullous skin diseaseRecruitingPhase 1 / Phase 22026-03-18NCT07193134

1 results · Page 1 of 1

Swipe the table sideways for more columns.

OrganizationsLinked trials
CHU de Quebec-Universite Laval54

1 results · Page 1 of 1

Swipe the table sideways for more columns.

Research sitesCityCountryLinked trials
The Hospital for Sick Children (SickKids)TorontoCanada3