drugset / Trial / NCT00698022

A 4-week Study of Mifepristone in the Prevention of Risperidone-induced Weight Gain in Healthy Male Volunteers

NCT00698022

Phase 1 Completed 76 enrolled Corcept Therapeutics
RandomizedSingle-groupTriple-blindPrevention

Summary

This is a 28-day, single-center, double-blind, placebo-controlled inpatient study of the administration of risperidone alone or in combination with mifepristone in healthy adult male volunteers to determine the average change in absolute weight at Day 28 compared to baseline.

Timeline

Start
2008-11
Primary completion
2009-02
Completion
2009-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Mifepristone Small molecule
Subject Risperidone Other / unclassified

Indications

No indication recorded.