drugset / Trial / NCT00216255

EXPRESS: Examining Pagoclone for Persistent Developmental Stuttering Study

NCT00216255 ↗

Phase 2 Completed 120 enrolled Endo USA Inc., a Keenova Therapeutics Company
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The objective of the study is to determine the effects of pagoclone on the symptoms of Persistent Developmental Stuttering, using a flexible dosing titration regimen on persistent developmental stuttering in patients 18 to 65 years of age.

Timeline

Start
2005-04
Primary completion
2011-07
Completion
2011-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Pagoclone Small molecule 0.15 mg —
Subject Pagoclone Small molecule 0.3 mg —
Subject Pagoclone Small molecule 0.6 mg —

Indications