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This study evaluates AVI-4658, an antisense oligonucleotide (designed to restore the dystrophin protein via exon 51 skipping) in Duchenne Muscular Dystrophy (DMD). It included boys aged 10-17 with biopsy-confirmed dystrophin defects and eligible gene deletions. It was a Phase 1/Phase 2 study and has been completed.
The summary above is a plain-language rendering of the official record. The original English title is shown for reference.
Criteria are reproduced from the ClinicalTrials.gov record in the original English. Only the trial team can determine eligibility.
Inclusion Criteria: 1. Subject is male ≥ 10 years and ≤ 17 years of age at the time of study drug administration. 2. Subject has clinical diagnosis compatible with Duchenne's Muscular Dystrophy (DMD) and evidence of mutational and dystrophin defects from muscle biopsy consistent with DMD (out-of frame deletions, absent dystrophin).Eligible deletions are those that can be rescued by the skipping of exon 51 \[45-50; 47-50; 48-50; 49-50; 50; 52; 52-63\]. 3. Subject has had a muscle biopsy analysed, showing \<5% revertant fibres present. Biopsy may be collected at the time of DMD diagnosis or as part of protocol screening procedures. 4. Subject is unable to ambulate or stand independently. 5. Subject has Stage 1 to 3 EDB muscle preservation determined by MRI. 6. Subject has a forced vital capacity ≥ 25% confirmed within 3 months from Day One. 7. Subject has mean oxygen saturation monitoring \> 94% in overnight domiciliary overnight sleep study within 3 months of Day One. 8. Subject has the ability to comply with all study evaluations and return for all study. 9. Subject and parent have psychiatric adjustments, adequately supportive psychosocial circumstances and a full understanding of study aims process and likely outcomes. Exclusion Criteria: 1. Subject has had external digitorum brevis (EDB) muscle removed. 2. Subject has Stage 4 EDB muscle preservation determined by MRI. 3. Subject has a left ventricular shortening fraction of \< 25% and/or an ejection fraction of \< 35% by echocardiography at visit one or within three months of visit one. 4. Subject has evidence of nocturnal hypoventilation (mean oxygen saturation at night of ≤ 94%) confirmed via overnight sleep study at Visit One (as screening procedure) or within 3 months of Visit One by overnight sleep study. 5. Subject has severe respiratory insufficiency defined by the need for invasive or non-invasive mechanical ventilation (does not include nocturnal ventilatory support). 6. Subject has severe cognitive dysfunction rendering them unable to understand and collaborate with study protocol. 7. Subject has immune deficiency or autoimmune disease. 8. Subject has a known bleeding disorder or has received chronic anticoagulant treatment within three months of study entry. 9. Subject has received pharmacologic treatment, apart from corticosteroids, that might affect muscle strength or function within 8 weeks of study entry (viz.,anabolic steroids, creatine protein supplementation, albuterol or other beta agonists). 10. Subject has had surgery within 3 months of study entry or planned for anytime during study. 11. Subject has active significant illness at time of study entry. 12. Subject has is unable to undergo MRI testing (viz., has metal implants). 13. Subject or parent has active psychiatric disorder, has adverse psychosocial circumstances, recent significant emotional loss, history of depressive or anxiety disorders that might interfere with protocol completion or compliance. 14. Subject has any known allergies to products likely to be used in the study (viz.,antiseptics, anaesthetics). 15. Subject has used any experimental treatments or has participated in any clinical trial within 4 weeks of study entry. 16. Subject has used intranasal, inhaled or topical steroids for a condition other than muscular dystrophy within 1 weeks of study entry.