drugset / Trial / NCT05285540

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

NCT05285540 ↗

Phase 1 Completed 39 enrolled Design Therapeutics, Inc.
RandomizedSequentialQuadruple-blindTreatment

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.

Timeline

Start
2022-03-11
Primary completion
2022-12-19
Completion
2022-12-19

Drugs

EvaluationDrugModalityDoseRoute
Subject DT-216 Unknown — Intravenous

Indications