Safety, Tolerability, and Pharmacokinetics of Single and Multiple Doses of HT-100 in Duchenne Muscular Dystrophy
Duchenne Muscular Dystrophy
About this trial
This is an interventional treatment trial for Duchenne Muscular Dystrophy focused on measuring halofuginone hydrobromide, anti-fibrotic, anti-inflammatory, muscle regeneration, protein synthesis inhibitor
Eligibility Criteria
Main Inclusion Criteria:
- Ambulatory or non-ambulatory
- Diagnosis of DMD with confirmation of minimal to no dystrophin
- Corticosteroid naive or on therapy for at least 12 months (stable dose and regimen)
Main Exclusion Criteria:
- Recent, substantial change in use of cardiac medications or medications affecting muscle function
- Inability to undergo magnetic resonance imaging (MRI)
- Significantly compromised cardio-respiratory function
- Prior treatment with another investigational product in past 6 months
Sites / Locations
- University of California, Davis Medical Center
- Kennedy Krieger Institute, Johns Hopkins School of Medicine
- Washington University School of Medicine
- Cincinnati Children's Hospital Medical Center
- Nationwide Children's Hospital
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm 5
Arm 6
Experimental
Experimental
Experimental
Experimental
Experimental
Experimental
Cohort 1: HT-100 tablet, Dose 1
Cohort 2: HT-100 tablet, Dose 2
Cohort 3: HT-100 tablet, Dose 3
Cohort 4a: HT-100 tablet, Dose 4
Cohort 4b: HT-100 tablet, Dose 5
Cohort 5: HT-100 tablet, Dose 6
Single dose administration: Dose 1 Multiple dose administration: Dose 1
Single dose administration: Dose 2 Multiple dose administration: Dose 2
Single dose administration: Dose 3 Multiple dose administration: Dose 3
Single dose administration: Dose 4 Multiple dose administration: Dose 4
* Multiple dose administration: Dose 5
* Multiple dose administration: Dose 5