Safety and Cognitive Function Study of EVP-6124 in Patients With Schizophrenia



Status:Completed
Conditions:Cognitive Studies, Cognitive Studies, Schizophrenia, Neurology
Therapuetic Areas:Neurology, Psychiatry / Psychology
Healthy:No
Age Range:18 - 55
Updated:10/14/2017
Start Date:December 2009
End Date:March 2011

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A Randomized Double-Blind Placebo-Controlled 12-Week Phase 2 Study of Two Different Doses of an Alpha-7 Nicotinic Acetylcholine Receptor Agonist(EVP-6124)or Placebo in Schizophrenia Subjects on Chronic Stable Atypical Anti-Psychotic Therapy

This study is being conducted to determine the safety and effect on cognitive function of two
different doses of an investigational medication, EVP-6124, in individuals with schizophrenia
who are on chronic stable atypical anti-psychotic therapy. In addition, behavioral and
psychotic symptoms will be evaluated.

This is a randomized, double-blind, placebo-controlled, Phase 2 safety/efficacy study in
which two dose levels of EVP-6124 will be evaluated. Eligible for enrollment will be patients
who meet clinical criteria for schizophrenia and who are taking chronic atypical
anti-psychotic medication at a stable dose. This study will therefore evaluate the effects of
EVP-6124 when administered concomitantly with anti-psychotic medication.

Patients will be randomized to one of the following groups: 0.3 mg or 1.0 mg EVP-6124, or
placebo. Seventy-five patients per group. Study drug will be supplied as capsules and will be
orally administered once daily for a total of 84 days.

Inclusion Criteria:

- Subjects who meet clinical criteria for schizophrenia or schizo-affective disorder
utilizing the structured clinical interview (SCI)

- Must be treated with a second generation anti-psychotic drug other than clozapine at a
stable dose for at least 4 weeks and must have been on that drug and clinically stable
for at least 8 weeks

- Must have no more than "moderate" severity rating for negative symptoms: BPRS item ≤4

- A minimal level of extrapyramidal symptoms (EPS); Simpson-Angus Scale total score ≤6

- A minimal level of depression; Calgary Depression Scale total score ≤10

- Must have a general health status acceptable for participation in a 12-week clinical
trial

- Fluency (oral and written) in the language in which the standardized tests will be
administered

- If a smoker, the ability to refrain from smoking for at least 30 minutes prior to any
cognitive testing

Exclusion Criteria:

General

- Insufficiently controlled diabetes mellitus in the judgment of the investigator

- Malignant tumor within the last 5 years with the exception of squamous and basal cell
carcinoma or cervical carcinoma it situ

- Pregnancy, nursing, (or if fertile female) not willing to utilize birth control
measures during study

- Unstable medical condition that is clinically significant in the judgment of the
investigator: major organ system dysfunction
We found this trial at
15
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Austin, Texas 78756
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Arkhangelsk,
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Charleston, South Carolina 29405
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Charleston, SC
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Chicago, Illinois 60640
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Chicago, IL
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DeSoto, Texas 75115
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DeSoto, TX
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222 West Eulalia Street
Glendale, California 91204
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Glendale, CA
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1650 Moon Lake Boulevard
Hoffman Estates, Illinois 60169
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Hoffman Estates, IL
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Nashville, Tennessee 37212
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Nashville, TN
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North Miami, Florida 33161
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North Miami, FL
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Oceanside, California 92056
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Oceanside, CA
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Rockville, Maryland 20850
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Rockville, MD
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San Diego, California 92093
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San Diego, CA
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San Diego, California 92108
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San Diego, CA
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Sherman Oaks, California 91403
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Sherman Oaks, CA
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Willingboro, New Jersey 08046
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Willingboro, NJ
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