drugset / Trial / NCT06411912

A Study of NIDO-361 in Patients With SBMA

NCT06411912 ↗

Phase 2 Completed 54 enrolled Nido Biosciences, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to evaluate the safety, tolerability, and efficacy of NIDO-361 in adult patients with Spinal and Bulbar Muscular Atrophy (SBMA).

Timeline

Start
2024-03-01
Primary completion
2025-10-22
Completion
2025-10-22

Drugs

EvaluationDrugModalityDoseRoute
Subject NIDO-361 Unknown 200 mg Oral