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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00259922
Other study ID # SB-767905/013
Secondary ID
Status Completed
Phase Phase 3
First received November 29, 2005
Last updated September 1, 2015
Start date August 2005

Study information

Verified date September 2009
Source Cubist Pharmaceuticals LLC
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

Adults who are taking opioid therapy for persistent non-cancer pain and have resulting opioid-induced bowel dysfunction (OBD) will be randomized (1:1:1) to one of 2 alvimopan arms, or to placebo. The primary objective of this phase 3 confirmatory study is to compare alvimopan with placebo for efficacy in the treatment of OBD. The primary efficacy endpoint is based on frequency of bowel movements. Subjects will be required to: (1) track their bowel movements and other bowel symptoms and (2) attend 6 clinic visits over 4 months.


Recruitment information / eligibility

Status Completed
Enrollment 485
Est. completion date
Est. primary completion date June 2006
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion criteria:

- Consented to participate in this study.

- Taking opioid therapy for persistent non-cancer pain.

- Has bowel dysfunction mainly due to opioids.

- Has bowel dysfunction since starting opioids as defined by infrequent bowel movements and additional bowel-related symptoms.

- Willing to discontinue laxative therapy (will be provided study-specific standardized laxative if needed).

- Willing to report daily bowel symptoms.

Exclusion criteria:

- Pregnant, lactating, or planning to become pregnant.

- Not ambulatory.

- Participated in another trial with an investigational drug in the past 30 days.

- Taking opioids for the management of drug addiction or cancer-related pain.

- Severe constipation whereby the subject is at immediate risk of developing serious complications of constipation.

- Gastrointestinal or pelvic disorders known to affect bowel transit, produce gastrointestinal (GI) obstruction, or contribute to bowel dysfunction.

- HIV-infected, has active hepatitis, or has ever been infected with hepatitis C.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Intervention

Drug:
Placebo
Placebo
Alvimopan
0.5 mg QD
Alviompan
0.5 mg BID

Locations

Country Name City State
Australia GSK Investigational Site Bedford Park South Australia
Australia GSK Investigational Site Box Hill Victoria
Australia GSK Investigational Site Broadmeadow New South Wales
Australia GSK Investigational Site Carina Heights Queensland
Australia GSK Investigational Site Carlton Victoria
Australia GSK Investigational Site Fremantle Western Australia
Australia GSK Investigational Site Kippa Ring Queensland
Australia GSK Investigational Site Nedlands Western Australia
Australia GSK Investigational Site Newcastle New South Wales
Australia GSK Investigational Site Port Lincoln South Australia
Australia GSK Investigational Site St Leonards New South Wales
Australia GSK Investigational Site Toorak Gardens South Australia
Canada GSK Investigational Site Bonaventure Quebec
Canada GSK Investigational Site Coquitlam British Columbia
Canada GSK Investigational Site Mississauga Ontario
Canada GSK Investigational Site Moncton New Brunswick
Canada GSK Investigational Site North Bay Ontario
Canada GSK Investigational Site North York Ontario
Canada GSK Investigational Site Saint Romuald Quebec
Canada GSK Investigational Site St. John's Newfoundland and Labrador
Canada GSK Investigational Site Sudbury Ontario
Canada GSK Investigational Site Trois-Rivieres Quebec
Canada GSK Investigational Site Winnipeg Manitoba
France GSK Investigational Site Boulogne
France GSK Investigational Site Grenoble
France GSK Investigational Site Montpellier Cedex 5
France GSK Investigational Site Paris
France GSK Investigational Site Paris
France GSK Investigational Site Paris Cedex 4
Hungary GSK Investigational Site Budapest
Hungary GSK Investigational Site Budapest
Hungary GSK Investigational Site Csongrád
Hungary GSK Investigational Site Heves
Netherlands GSK Investigational Site Alkmaar
Netherlands GSK Investigational Site Breda
Netherlands GSK Investigational Site Roosendaal
Netherlands GSK Investigational Site Rotterdam
Netherlands GSK Investigational Site Utrecht
New Zealand GSK Investigational Site Christchurch
New Zealand GSK Investigational Site Hamilton
New Zealand GSK Investigational Site Tauranga
Norway GSK Investigational Site Oslo
Norway GSK Investigational Site Oslo
Norway GSK Investigational Site Paradis
Norway GSK Investigational Site Rådahl
Norway GSK Investigational Site Skien
South Africa GSK Investigational Site Athlone, Cape Town
South Africa GSK Investigational Site Erasmuskloof, Pretoria
South Africa GSK Investigational Site Fourways, Johannesburg
South Africa GSK Investigational Site Kempton Park
South Africa GSK Investigational Site Kenilworth, Cape Town
South Africa GSK Investigational Site Lynnwood, Pretoria
South Africa GSK Investigational Site Tygervalley
South Africa GSK Investigational Site Westridge, Mitchells Plain
Spain GSK Investigational Site Alcorcon
Spain GSK Investigational Site Barcelona
Spain GSK Investigational Site El Ferrol
Spain GSK Investigational Site Granada
Spain GSK Investigational Site Madrid
Spain GSK Investigational Site Madrid
Spain GSK Investigational Site Santander
Spain GSK Investigational Site Valencia
Sweden GSK Investigational Site Jönköping
Sweden GSK Investigational Site Karlstad
Sweden GSK Investigational Site Linköping
Sweden GSK Investigational Site Stockholm
Switzerland GSK Investigational Site Bern
Switzerland GSK Investigational Site Nottwil
United States GSK Investigational Site Albuquerque New Mexico
United States GSK Investigational Site Asheville North Carolina
United States GSK Investigational Site Atlanta Georgia
United States GSK Investigational Site Atlanta Georgia
United States GSK Investigational Site Austin Texas
United States GSK Investigational Site Bakersfield California
United States GSK Investigational Site Beverly Hills California
United States GSK Investigational Site Birmingham Alabama
United States GSK Investigational Site Birmingham Alabama
United States GSK Investigational Site Blackwood New Jersey
United States GSK Investigational Site Boston Massachusetts
United States GSK Investigational Site Brockton Massachusetts
United States GSK Investigational Site Centerville Ohio
United States GSK Investigational Site Charleston West Virginia
United States GSK Investigational Site Chicago Illinois
United States GSK Investigational Site Chiefland Florida
United States GSK Investigational Site Cincinnati Ohio
United States GSK Investigational Site Clearwater Florida
United States GSK Investigational Site Corpus Christi Texas
United States GSK Investigational Site Cranston Rhode Island
United States GSK Investigational Site Cumming Georgia
United States GSK Investigational Site Dayton Ohio
United States GSK Investigational Site Deerfield Beach Florida
United States GSK Investigational Site Destin Florida
United States GSK Investigational Site Dover New Hampshire
United States GSK Investigational Site Egg Harbor Township New Jersey
United States GSK Investigational Site Eugene Oregon
United States GSK Investigational Site Evansville Indiana
United States GSK Investigational Site Fort Myers Florida
United States GSK Investigational Site Galveston Texas
United States GSK Investigational Site Greensboro North Carolina
United States GSK Investigational Site Greer South Carolina
United States GSK Investigational Site Hickory North Carolina
United States GSK Investigational Site Hollywood Florida
United States GSK Investigational Site Hollywood Florida
United States GSK Investigational Site Houston Texas
United States GSK Investigational Site Huntsville Alabama
United States GSK Investigational Site Independence Missouri
United States GSK Investigational Site Indianapolis Indiana
United States GSK Investigational Site Kingsport Tennessee
United States GSK Investigational Site La Crosse Wisconsin
United States GSK Investigational Site Largo Florida
United States GSK Investigational Site Las Vegas Nevada
United States GSK Investigational Site Las Vegas Nevada
United States GSK Investigational Site Las Vegas Nevada
United States GSK Investigational Site Las Vegas Nevada
United States GSK Investigational Site Levittown Pennsylvania
United States GSK Investigational Site Lexington Kentucky
United States GSK Investigational Site Libertyville Illinois
United States GSK Investigational Site Long Beach California
United States GSK Investigational Site Los Angeles California
United States GSK Investigational Site Los Gatos California
United States GSK Investigational Site Louisville Kentucky
United States GSK Investigational Site Margate Florida
United States GSK Investigational Site Marietta Georgia
United States GSK Investigational Site Medford Oregon
United States GSK Investigational Site Meridian Idaho
United States GSK Investigational Site Mesa Arizona
United States GSK Investigational Site Miami Florida
United States GSK Investigational Site Miami Florida
United States GSK Investigational Site Miami Florida
United States GSK Investigational Site Mineola New York
United States GSK Investigational Site Missoula Montana
United States GSK Investigational Site Mobile Alabama
United States GSK Investigational Site New Tazewell Tennessee
United States GSK Investigational Site New York New York
United States GSK Investigational Site Norfolk Virginia
United States GSK Investigational Site Northport Alabama
United States GSK Investigational Site Northridge California
United States GSK Investigational Site Oak Forest Illinois
United States GSK Investigational Site Oakbrook Terrace Illinois
United States GSK Investigational Site Ocala Florida
United States GSK Investigational Site Olive Branch Mississippi
United States GSK Investigational Site Orange California
United States GSK Investigational Site Ormond Beach Florida
United States GSK Investigational Site Palm Springs California
United States GSK Investigational Site Pasadena California
United States GSK Investigational Site Pasadena Maryland
United States GSK Investigational Site Perrysburg Ohio
United States GSK Investigational Site Phoenix Arizona
United States GSK Investigational Site Pittsburgh Pennsylvania
United States GSK Investigational Site Portage Michigan
United States GSK Investigational Site Portland Oregon
United States GSK Investigational Site Raleigh North Carolina
United States GSK Investigational Site Reading Pennsylvania
United States GSK Investigational Site Richardson Texas
United States GSK Investigational Site Richmond Virginia
United States GSK Investigational Site Rochester New York
United States GSK Investigational Site Rockville Maryland
United States GSK Investigational Site Sacramento California
United States GSK Investigational Site Salem Oregon
United States GSK Investigational Site Salt Lake City Utah
United States GSK Investigational Site San Antonio Texas
United States GSK Investigational Site San Antonio Texas
United States GSK Investigational Site San Diego California
United States GSK Investigational Site San Rafael California
United States GSK Investigational Site Santa Ana California
United States GSK Investigational Site Scottsdale Arizona
United States GSK Investigational Site Scottsdale Arizona
United States GSK Investigational Site Spokane Washington
United States GSK Investigational Site St. Cloud Florida
United States GSK Investigational Site St. Louis Missouri
United States GSK Investigational Site St. Louis Missouri
United States GSK Investigational Site Stamford Connecticut
United States GSK Investigational Site Stockbridge Georgia
United States GSK Investigational Site Sunset Louisiana
United States GSK Investigational Site Tacoma Washington
United States GSK Investigational Site Tampa Florida
United States GSK Investigational Site Tempe Arizona
United States GSK Investigational Site Tucson Arizona
United States GSK Investigational Site Tucson Arizona
United States GSK Investigational Site Washington District of Columbia
United States GSK Investigational Site Waterbury Connecticut
United States GSK Investigational Site Waterford Michigan
United States GSK Investigational Site Wellesley Hills Massachusetts
United States GSK Investigational Site West Palm Beach Florida
United States GSK Investigational Site Winston-Salem North Carolina
United States GSK Investigational Site Winterhaven Florida
United States GSK Investigational Site Yakima Washington

Sponsors (2)

Lead Sponsor Collaborator
Cubist Pharmaceuticals LLC GlaxoSmithKline

Countries where clinical trial is conducted

United States,  Australia,  Canada,  France,  Hungary,  Netherlands,  New Zealand,  Norway,  South Africa,  Spain,  Sweden,  Switzerland, 

References & Publications (1)

Irving G, Pénzes J, Ramjattan B, Cousins M, Rauck R, Spierings EL, Kleoudis CS, Snidow JW, Pierce A, Wurzelmann J, Mortensen ER. A randomized, placebo-controlled phase 3 trial (Study SB-767905/013) of alvimopan for opioid-induced bowel dysfunction in pati — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary To compare alvimopan with placebo for efficacy in the treatment of OBD
Secondary Safety and tolerability, quality of life, pharmacogenetics (dependent on results from other data)
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