Clinical Trials Directory

Trials / Unknown

UnknownNCT00604760

Study to Evaluate the Safety and Efficacy of MEM 3454 as Adjunctive Treatment in Combination With a Preexisting Antipsychotic in Patients With Cognitive Impairment Associated With Schizophrenia

A Phase 2a, Multi-Center, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study to Evaluate the Safety and Efficacy of MEM 3454 as Adjunctive Treatment in Combination With a Preexisting Antipsychotic in Patients With Cognitive Impairment Associated With Schizophrenia

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

Summary

To establish the proof of concept that MEM 3454, used as add-on pharmacotherapy, is a safe and effective treatment in patients with cognitive impairment associated with schizophrenia (CIAS).

Conditions

Interventions

TypeNameDescription
DRUGMEM 3454Capsule 5 mg once a day
DRUGMEM 3454Capsule 15 mg once a day
DRUGMEM 3454Capsule 50 mg once a day
DRUGPlacebo for MEM 3454Capsule once a day

Timeline

Start date
2007-12-01
Primary completion
2009-02-01
First posted
2008-01-30
Last updated
2008-12-08

Locations

44 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00604760. Inclusion in this directory is not an endorsement.