drugset / Trial / NCT06830642

Study of the Oral Treatment MTR-601 in Cervical Dystonia

NCT06830642 ↗

Phase 2 Suspended 80 enrolled Motric Bio
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Study MTR-601-201 is an 8-week, randomized, placebo-controlled study to examine the safety, tolerability, and efficacy of MTR-601 in participants with cervical dystonia.

Timeline

Start
2025-02-28
Primary completion
2026-07-08
Completion
2026-08-03

Outcome

Outcome not reported

Stopped: “Pending further safety evaluation”

Drugs

EvaluationDrugModalityDoseRoute
Subject MTR-601 Unknown — Oral

Indications