← Eichor
Study identifier: NCT07287189 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Phase 2 Study of SAT-3247 in Pediatric Ambulatory Patients

Condition: Duchenne Muscular Dystrophy · Duchenne · DMD  ·  Sponsor: Satellos Bioscience, Inc.

PhasePhase 2
Planned participants51
Who can joinMale, 7 Years to 9 Years
Healthy volunteersNo

About this study

Phase 2a trial of SAT-3247 in ambulatory DMD patients aged ≥ 7 and \< 10 years. The trial will study two doses of SAT-3247 in a randomized, double-blind, placebo-controlled weekday regimen for 12 weeks to determine the optimal dose, safety, tolerability, and preliminary efficacy.

This description comes directly from the study's public registry record.

Talk to the study team

Satellos Medical Information  ·  +1 647-660-1780  ·  medicalinfo@satellos.com

Always discuss trial participation with your own doctor first.

Locations (21)

University of California Los AngelesLos Angeles, California, United StatesRecruiting
Colorado Children'sAurora, Colorado, United StatesRecruiting
Lurie Children'sChicago, Illinois, United StatesRecruiting
UMass Memorial Medical CenterWorcester, Massachusetts, United StatesRecruiting
Washington UniversitySt Louis, Missouri, United StatesRecruiting
Nationwide Children's HospitalColumbus, Ohio, United StatesRecruiting
Seattle Children'sSeattle, Washington, United StatesRecruiting
Children's Hospital at WestmeadWestmead, New South Wales, AustraliaNot Yet Recruiting
Royal Children's Hospital MelbourneMelbourne, Victoria, AustraliaRecruiting
Hôpital De La Citadelle (CHR)Liège, Liège, BelgiumRecruiting
UZ GentGhent, Oost-Vlaanderen, BelgiumRecruiting
Children's Hospital Eastern OntarioOttawa, Ontario, CanadaRecruiting

+ 9 more locations — full list on the registry record.

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07287189