Condition: Duchenne Muscular Dystrophy (DMD) · Sponsor: Shanghai Siponuoyin Biotechnology Co Ltd
The primary objective of this study is to evaluate the safety and tolerability of SPOT-03 administered by intravenous (IV) infusion to DMD patients. In addition, this study will preliminarily investigate the changes in dystrophin nucleic acid concentration, dystrophin protein expression and engraftment, anti-dystrophin antibodies and cytokine profiles, as well as fat tissue mas and lean tissue mass following SPOT-03 administrations.
This description comes directly from the study's public registry record.
Winston Town · 212-920-5501 · Winston.town@spotbiosystems.com
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| Shanghai Children's Medical Center | Shanghai, Shanghai Municipality, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07188012