Muscle function, linear growth, and bone health during 30 months of vamorolone, prednisone, and deflazacort treatment for Duchenne muscular dystrophy: a comparative study
Corticosteroids are standard of care to slow disease progression in Duchenne muscular dystrophy (DMD) despite impaired growth and increased fracture risk. Vamorolone, a dissociative corticosteroid approved for DMD, showed stable growth and serum bone turnover markers in the 48-week VISION-DMD study. We compared muscle function and bone health from the non-randomized, open-label, 30-month Phase 2a VBP15-002/003/LTE trials (NCT02760264/NCT02760277/NCT03038399) in treatment-naive boys with DMD, aged 4 to <7 years at baseline, with data from matched corticosteroids-treated boys from FOR-DMD (NCT01603407). Motor function by slope-of-change analysis was evaluated for vamorolone 2-6 mg/kg/d through 30 months compared with propensity score-matched boys from FOR-DMD who received daily prednisone (starting dosage 0.75 mg/kg/d) or deflazacort (0.9 mg/kg/d) for 36 months. Anthropometric and bone assessments were performed in boys on vamorolone for 30 months, including those who received lower dosages during VBP15-002/003 (0.25/0.75 mg/kg/d for 6 months). Vertebral fracture (VF) prevalence was compared with baseline-matched FOR-DMD data. Thirty-month vamorolone VF results were adjusted to approximate expected fracture prevalence at 36 months. All slope-of-change motor function comparisons between vamorolone (N=22) and prednisone (N=32) or deflazacort (N=34) groups yielded no significant differences (p>0.05). Thirty-month height z-scores remained stable from baseline for vamorolone (N=36; +0.078 least-squares-mean change) and decreased from baseline for prednisone (N=27, -0.668; change versus vamorolone: p<0.0001 mixed models for repeat measures) and deflazacort (N=28, -0.928; change versus vamorolone: p<0.0001). VF prevalence on vamorolone (8 VF in 5/39 boys [12.8%]) was ~50% lower than prednisone (13 VF in 7/27 boys [25.9%]) and deflazacort (19 VF in 8/28 boys [28.6%]). Compared with prednisone and deflazacort, vamorolone demonstrated similar motor function efficacy with significantly fewer VF and preserved growth.
Authors
- Raoul Rooman (ORCID: https://orcid.org/0000-0003-3061-3388)
- Michela Guglieri (ORCID: https://orcid.org/0000-0002-8455-0637)
- Jacob Lester Jaremko (ORCID: https://orcid.org/0000-0001-5314-2297)
- Utkarsh J. Dang (ORCID: https://orcid.org/0000-0003-4120-2015)
- Nazih F. Shenouda
- Kerry G. Siminoski
- Khaldoun Koujok
- Stefan A. Jackowski (ORCID: https://orcid.org/0000-0002-0544-9240)
- Leanne Marie Ward (ORCID: https://orcid.org/0000-0003-1557-9185)
- Hugh J. McMillan (ORCID: https://orcid.org/0000-0001-8927-2018)
- Eric P. Hoffman (ORCID: https://orcid.org/0000-0001-6470-5139)
- Shabir Hasham (ORCID: https://orcid.org/0000-0003-4672-8825)
- Paula R. Clemens (ORCID: https://orcid.org/0000-0002-0652-6703)
- Mary‐Ann Matzinger
- Mika Leinonen
- Maya Scharke B Comm (ORCID: https://orcid.org/0009-0000-6392-8648)
Institutions
- Binghamton University (US)
- University of Ottawa (CA)
- University of Alberta (CA)
- University of Pittsburgh (US)
- Children's Hospital of Eastern Ontario (CA)
- Newcastle upon Tyne Hospitals NHS Foundation Trust (GB)
- Santhera Pharmaceuticals (Switzerland) (CH)
- ReveraGen BioPharma (United States) (US)
- Anthera Pharmaceuticals (United States) (US)
- Carleton University (CA)
- Newcastle University (GB)
Publication Details
- Journal
- Journal of Bone and Mineral Research
- Published
- 2026-10-29
- DOI
- https://doi.org/10.1093/jbmr/zjag154
- Primary Topic
- Muscle Physiology and Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- U.S. Department of Defense
- Foundation to Eradicate Duchenne
- Muscular Dystrophy Association
- Parent Project Muscular Dystrophy
- Canadian Institute for Advanced Research
- University of Ottawa
- National Institute for Health and Care Research
- Newcastle University
- European Commission
- National Institutes of Health
- NIHR Newcastle Biomedical Research Centre
- National Institute of Neurological Disorders and Stroke
- National Institute of Child Health and Human Development
- Eunice Kennedy Shriver National Institute of Child Health and Human Development