Study To Examine Effect Of CP-866,087 On Consumption And Craving Of Alcohol In Alcohol Dependent Subjects.

Completed · Phase 2

Conditions studied: Alcoholism

In brief

Test the hypothesis that increasing doses of CP-866,087 will decrease the total number of drinks consumed during a 2 hour acute alcohol consumption assessment and to determine the safety and tolerability of multiple doses of CP-866,087 in alcohol dependent subjects compared to placebo.

Key facts

Study ID

NCT00147576

Run by

Pfizer

People needed

88

Starts

2003-12-01

Expected to finish

2004-12-01

Last updated by the study team

2012-10-02

Who can join

Age: 21 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subject meets the DSM-IV criterion for current alcohol dependence.
• Subject is currently not engaged in, and does not want, treatment for alcohol related problems.

You may not qualify if…

• Subject meets criteria for current DSM-IV diagnosis for any other psychoactive substance abuse or dependence disorder, excluding nicotine and caffeine.
• Specialized inpatient or outpatient alcoholism or other addiction treatment (except nicotine) within the past 12 months.

Where it is running

• Pfizer Investigational Site — Cerritos, California, United States
• Pfizer Investigational Site — New Haven, Connecticut, United States
• Pfizer Investigational Site — New Haven, Connecticut, United States
• Pfizer Investigational Site — Washington D.C., District of Columbia, United States
• Pfizer Investigational Site — Melbourne, Florida, United States
• Pfizer Investigational Site — Melbourne, Florida, United States
• Pfizer Investigational Site — Lenexa, Kansas, United States
• Pfizer Investigational Site — Providence, Rhode Island, United States
• Pfizer Investigational Site — Charleston, South Carolina, United States
• Pfizer Investigational Site — San Antonio, Texas, United States
• Pfizer Investigational Site — San Antonio, Texas, United States

Full record on ClinicalTrials.gov

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