Clinical Trials Directory

Trials / Unknown

UnknownNCT00725855

A Single-Center, Double-Blind (DB) Study of MEM 3454 on P50 Sensory Gating and Mismatch Negativity in Schizophrenia Patients

A Single-Center, Double-Blind, Placebo-Controlled, Randomized Blocks Study Investigating the Effect of 4 Dosages (1 mg, 5 mg, 15 mg, 50 mg) of MEM 3454 on P50 Sensory Gating and Mismatch Negativity (MMN) in Patients With Schizophrenia

Status
Unknown
Phase
Phase 2
Study type
Interventional
Enrollment
12 (estimated)
Sponsor
Memory Pharmaceuticals · Industry
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the effects of nicotinic alpha-7 MEM 3454 on P50 sensory gating in patients with Schizophrenia. The hypothesis is that MEM 3454 will normalize the P50 ratio. Data produced in this study will provide useful information regarding the value of P50 as an efficacy biomarker, and provide evidence for the optimal dosing of MEM 3454 for additional P50 studies.

Conditions

Interventions

TypeNameDescription
DRUGMEM 34541 mg dose
DRUGMEM 34545 mg dose
DRUGMEM 345415 mg dose
DRUGMEM 345450 mg dose
DRUGPlacebo for MEM 3454Placebo dose

Timeline

Start date
2008-08-01
Primary completion
2009-03-01
Completion
2009-04-01
First posted
2008-07-31
Last updated
2008-07-31

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00725855. Inclusion in this directory is not an endorsement.