Study of SPG601 in Adult Men With Fragile X Syndrome

Status Recruiting

Clinical Trial Summary

This Phase 2 study described herein will evaluate the safety, efficacy, tolerability, pharmacokinetics and pharmacodynamics of SPG601 in adult men with Fragile X syndrome.

Clinical Trial Description

This study is a Phase 2 randomized, double blind, placebo-controlled, cross over, single dose of SPG601 and matching Placebo in patients with Fragile X syndrome. This study will entail 2 in person clinic visits to administer oral doses of SPG601 or matching placebo. Participants will receive a dose of either SPG601 or placebo at first visit, and will cross over to receive the other product at the second visit. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06413537
Study type	Interventional
Source	Spinogenix
Contact	Sarah Richter
Phone	513-803-3324
Email	sarah.richter@cchmc.org
Status	Recruiting
Phase	Phase 2
Start date	June 18, 2024
Completion date	February 2025

View Details

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