Study to Evaluate DT-216 in Adult Patients With Friedreich Ataxia

  • participants needed
  • sponsor
    Design Therapeutics
Updated on 28 January 2023
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The purpose of this study is to evaluate the safety, tolerability, pharmacokinetic and pharmacodynamic effects of intravenous DT-216 in adult patients with Friedreich Ataxia. This single ascending dose study is randomized, double-blind, placebo-controlled.

Condition Friedreich Ataxia
Treatment DT-216, DT-216 matching Placebo
Clinical Study IdentifierNCT05285540
SponsorDesign Therapeutics
Last Modified on28 January 2023

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