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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
A Study of FCX-007 for Recessive Dystrophic Epidermolysis BullosaCollagen Diseases, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, 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 diseaseActive, not recruitingPhase 32026-03-18NCT04213261

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OrganizationsLinked trials
Castle Creek Biosciences, LLC.2

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Research sitesCityCountryLinked trials
Children's Hospital ColoradoAuroraUnited States312
Dell Children'S Medical GroupAustinUnited States4
Mayo ClinicRochesterUnited States664
Solutions Through Advanced Research, Inc.JacksonvilleUnited States2
Stanford UniversityStanfordUnited States213