Stopped: Sponsor decision not related to safety concerns
The primary objective of the study is to evaluate the safety of UX053 in adults with Glycogen Storage Disease Type III (GSD III).
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Number of Participants With Treatment-Emergent Adverse Events (TEAEs), Serious TEAEs, Deaths, Discontinuations, and/or Dose Changes
Timeframe: From first dose of study drug through the end of study (up to Day 90)