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Completed Phase 2 Interventional

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

ClinicalTrials.gov ID: NCT00147576

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This page only displays public information reproduced from the official ClinicalTrials.gov record NCT00147576. It adds no medical advice, opinions, or eligibility judgments. The official record remains the source of truth for eligibility criteria, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 13, 2026, 11:26 PM EST

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Official title

Randomized, Placebo-Controlled Parallel Group Study Comparing Effect Of Three Doses Of CP-866,087 And Naltrexone On Acute Alcohol Consumption And Craving After Seven Days Of Treatment In Alcohol Dependent (DSM IV) Subjects Who Are Not Currently Seeking Treatment

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT00147576
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
88 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
21 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 2003 (Type not available)
Primary completion
Not listed
Completion
Dec 2004 (Actual)
Last update posted
Oct 2, 2012

2003 – 2004

United States locations

U.S. sites
11
U.S. states
8
U.S. cities
8
Facility City State ZIP Site status
Pfizer Investigational Site Cerritos California 90703 —
Pfizer Investigational Site New Haven Connecticut 06504 —
Pfizer Investigational Site New Haven Connecticut 06519 —
Pfizer Investigational Site Washington D.C. District of Columbia 20016 —
Pfizer Investigational Site Melbourne Florida 32901 —
Pfizer Investigational Site Melbourne Florida 32935 —
Pfizer Investigational Site Lenexa Kansas 66219 —
Pfizer Investigational Site Providence Rhode Island 02908 —
Pfizer Investigational Site Charleston South Carolina 29425 —
Pfizer Investigational Site San Antonio Texas 78229-3900 —
Pfizer Investigational Site San Antonio Texas 78229 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00147576, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 2, 2012 · Synced Nov 13, 2026

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