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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Phase 2 Study of SAT-3247 in Pediatric Ambulatory PatientsCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne muscular dystrophy, Muscular Disorders, Atrophic, X-linked disease, hereditary disease, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, nervous system disorder, neuromuscular diseaseActive, not recruitingPhase 22026-10-02NCT07287189

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OrganizationsLinked trials
Satellos Bioscience, Inc.2

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Research sitesCityCountryLinked trials
Children's Hospital at WestmeadWestmeadAustralia9
Children's Hospital Eastern OntarioOttawaCanada1
Colorado Children'sAuroraUnited States1
Great Ormond StreetLondonUnited Kingdom1
Hospital Infantil i Hospital de la DonaBarcelonaSpain1
Hospital Universitario DonostiaDonostia / San SebastianSpain3
Hospital Universitario y Politécnico La FeValenciaSpain20
Hôpital De La Citadelle (CHR)LiègeBelgium1
Instytut Centrum Zdrowia Matki PolkiLodzPoland6
Klinika Neurologii Rozwojowej UniwersyteckieGdanskPoland1
Lurie Children'sChicagoUnited States2
Mother and Child Health Care InstituteBelgradeSerbia1
Nationwide Children's HospitalColumbusUnited States309
Royal Children's Hospital MelbourneMelbourneAustralia2
Seattle Children'sSeattleUnited States21
UMass Memorial Medical CenterWorcesterUnited States21
University Children's Clinic TirsovaBelgradeSerbia1
University of California Los AngelesLos AngelesUnited States87
UZ GentGhentBelgium36
Washington UniversitySt LouisUnited States182