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
| Type | Name | Description |
|---|---|---|
| DRUG | MEM 3454 | 1 mg dose |
| DRUG | MEM 3454 | 5 mg dose |
| DRUG | MEM 3454 | 15 mg dose |
| DRUG | MEM 3454 | 50 mg dose |
| DRUG | Placebo for MEM 3454 | Placebo 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.