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.

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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

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article

Muscle function, linear growth, and bone health during 30 months of vamorolone, prednisone, and deflazacort treatment for Duchenne muscular dystrophy: a comparative study

Raoul Rooman, Michela Guglieri, Jacob Lester Jaremko, Utkarsh J. Dang et al.
2 links
Journal of Bone and Mineral Research
Muscle Physiology and Disorders
article

Muscle function, linear growth, and bone health during 30 months of vamorolone, prednisone, and deflazacort treatment for Duchenne muscular dystrophy: a comparative study

Raoul Rooman, Michela Guglieri, Jacob Lester Jaremko, Utkarsh J. Dang, Nazih F. Shenouda, Kerry G. Siminoski, Khaldoun Koujok, Stefan A. Jackowski, Leanne Marie Ward, Hugh J. McMillan, Eric P. Hoffman, Shabir Hasham, Paula R. Clemens, Mary‐Ann Matzinger, Mika Leinonen, Maya Scharke B Comm
article en

Abstract

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.

Journal of Bone and Mineral Research
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)
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
Good health and well-being
Openalex Percentile: Top 23%
Muscle Physiology and Disorders
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