Abstract | INTRODUCTION/AIMS: METHODS: Nineteen patients were enrolled and assigned to one of three dosing arms (5, 20, or 40 mg/kg every 4 weeks). After 32 weeks of treatment, participants receiving the lowest dose were switched to the highest dose (40 mg/kg) for an additional 32 weeks. An extension study was also conducted. The primary endpoints were safety and tolerability. Secondary endpoints included muscle strength, timed function testing, pulmonary function, lean body mass, pharmacokinetics, and pharmacodynamics. As an exploratory outcome, muscle fat fractions were derived from whole-body magnetic resonance images. RESULTS: Serum concentrations of domagrozumab increased in a dose-dependent manner and modest levels of myostatin inhibition were observed in both serum and muscle tissue. The most frequently occurring adverse events were injuries secondary to falls. There were no significant between-group differences in the strength, functional, or imaging outcomes studied. DISCUSSION:
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Authors | Doris G Leung, Alex E Bocchieri, Shivani Ahlawat, Michael A Jacobs, Vishwa S Parekh, Vladimir Braverman, Katherine Summerton, Jennifer Mansour, Nikia Stinson, Genila Bibat, Carl Morris, Shannon Marraffino, Kathryn R Wagner |
Journal | Muscle & nerve
(Muscle Nerve)
Vol. 64
Issue 2
Pg. 172-179
(08 2021)
ISSN: 1097-4598 [Electronic] United States |
PMID | 33961310
(Publication Type: Clinical Trial, Phase II, Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | © 2021 Wiley Periodicals LLC. |
Chemical References |
- Antibodies, Monoclonal, Humanized
- domagrozumab
- FKRP protein, human
- Pentosyltransferases
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Topics |
- Adult
- Antibodies, Monoclonal, Humanized
(therapeutic use)
- Body Composition
(drug effects)
- Female
- Humans
- Male
- Middle Aged
- Muscle Strength
(drug effects)
- Muscle, Skeletal
(drug effects, physiopathology)
- Muscular Dystrophies, Limb-Girdle
(drug therapy, physiopathology)
- Pentosyltransferases
(metabolism)
- Young Adult
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