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Completed Phase 2 Interventional

Study 767905/008 Extension Study: Alvimopan for Treatment of Opioid-Induced Bowel Dysfunction in Cancer Pain Subjects

ClinicalTrials.gov ID: NCT00135577

Public ClinicalTrials.gov record NCT00135577. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 3, 2026, 12:20 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Double-Blind, Placebo-Controlled, Multicenter Phase IIb Extension Study to Evaluate the Safety and Efficacy of Multiple Alvimopan Dosage Regimens for the Treatment of Opioid-Induced Bowel Dysfunction in Cancer Pain Subjects

Brief summary

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

Study SB-767905/008 was a multicenter study to evaluate the effectiveness and safety of multiple dosage regimens of an investigational drug for the treatment of constipation due to prescription pain medication in participants with cancer pain. Study ABD101684 will serve as an extension to Study SB-767905/008 and offer continued access to blinded investigational product to participants who have completed the original study. The purpose of Study ABD101684 is to evaluate the safety and efficacy of alvimopan compared to placebo in subjects who completed Study SB-767905/008 and elected to participate in this extension study.

Study identification

NCT ID
NCT00135577
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
67 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
Aug 31, 2004
Primary completion
Mar 31, 2007
Completion
Mar 31, 2007
Last update posted
Sep 1, 2015

2004 – 2007

United States locations

U.S. sites
14
U.S. states
7
U.S. cities
14
Facility City State ZIP Site status
GSK Investigational Site Duarte California 91010
GSK Investigational Site Fountain Valley California 92708
GSK Investigational Site La Verne California 91750
GSK Investigational Site Sacramento California 95819
GSK Investigational Site San Diego California 92103
GSK Investigational Site New Port Richey Florida 34652
GSK Investigational Site Tampa Florida 33612-9497
GSK Investigational Site West Des Moines Iowa 50265
GSK Investigational Site Boston Massachusetts 02215
GSK Investigational Site Worcester Massachusetts 01608
GSK Investigational Site St Louis Missouri 63141
GSK Investigational Site Durham North Carolina 27710
GSK Investigational Site Hendersonville North Carolina 28793
GSK Investigational Site Tacoma Washington 98405

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 26 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00135577, 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 Sep 1, 2015 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00135577 live on ClinicalTrials.gov.

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