Swipe the table sideways for more columns.

TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Filsuvez in Moderate-to-Severe Epidermolysis Bullosa SimplexCongenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin Abnormalities, Skin and Connective Tissue Diseases, epidermolysis bullosa, epidermolysis bullosa simplex, hereditary disease, hereditary skin disorder, skin disorder, vesiculobullous skin diseaseNot yet recruitingPhase 22026-08-10NCT07756138

1 results · Page 1 of 1

Swipe the table sideways for more columns.

OrganizationsLinked trials
Stanford University620

1 results · Page 1 of 1

Swipe the table sideways for more columns.

Research sitesCityCountryLinked trials
Stanford University School of MedicinePalo AltoUnited States18