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Clinical Trial Summary

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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05285540
Study type Interventional
Source Design Therapeutics
Contact
Status Completed
Phase Phase 1
Start date March 11, 2022
Completion date December 19, 2022

See also
  Status Clinical Trial Phase
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