New drug shows promise for improving walking in adults with spinal muscular atrophy
NCT ID NCT05794139
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested an experimental drug called NMD670 in 52 adults with type 3 spinal muscular atrophy who can still walk. The goal was to see if the drug helps them walk farther in 6 minutes and improves muscle strength compared to a placebo. The trial is now complete, and results will show whether NMD670 can ease symptoms of this muscle-weakening condition.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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AOU Città della Salute e della Scienza di Torino
Torino, Italy
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Aarhus Universitetshospital, Neurologisk Afdeling
Aarhus, Denmark
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CHR de la Citadelle - Neurologie
Liège, Belgium
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Charite - Campus Virchow-Klinikum (CVK)
Berlin, Germany
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Genge Partners Inc.
Montreal, Canada
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Heritage Medical Research Clinic
Calgary, Canada
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Hospital Materno Infantil La Paz
Madrid, Spain
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Hospital Universitari Vall D Hebron
Barcelona, Spain
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Hospital Universitario y Politécnico La Fe
Valencia, Spain
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Istituto Giannina Gaslini, IRCCS
Genova, Italy
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Istituto Neurologico C. Besta, Fondazione IRCCS
Milan, Italy
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Neurology Rare Disease Center
Denton, Texas, 76208, United States
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Ospedale Niguarda, ASST Grande Ospedale Metropolitano Niguarda
Milan, Italy
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Rare Disease Research - Raleigh-Durham
Hillsborough, North Carolina, 27278, United States
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Rigshospitalet - Neurologisk Afdeling
Copenhagen, Denmark
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Roy Blunt NextGen Precision Health Institute
Columbia, Missouri, 65212, United States
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Stanford University Medical Center
Palo Alto, California, 94304, United States
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The Johns Hopkins Medicine, Spinal Muscular Atrophy Center
Baltimore, Maryland, 21287, United States
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The Ohio State University Wexner Medical Center
Columbus, Ohio, 43210, United States
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UCLA David Geffen School Of Medicine - Neurology
Los Angeles, California, 90095, United States
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UZ Leuven - Neurochirurgie Campus Gasthuisberg
Leuven, Belgium
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Universitair Medisch Centrum Utrecht, locatie Academisch Zie - Neurology
Utrecht, Netherlands
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University of Kansas Medical Center
Kansas City, Kansas, 66160, United States
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Universitätsklinikum Essen - Klinik Für Neurologie
Essen, Germany
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Washington University School of Medicine
St Louis, Missouri, 63110, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can gene therapy help babies with SMA reach milestones? a Real-World review
- School transitions put to the test for children with a rare muscle disease
- Horseback therapy may boost movement and breathing in kids with Muscle-Weakening disease
- Newborn screening study aims to catch rare diseases at birth
- Gene therapy trial aims to halt Muscle-Wasting disease
- Higher dose of spinraza tested in SMA patients who already tried risdiplam