Study Of Alvimopan Drug For Treatment Of Constipation Due To Prescription Pain Medication

This study has been completed.
Sponsor:
Collaborator:
GlaxoSmithKline
Information provided by:
Cubist Pharmaceuticals
ClinicalTrials.gov Identifier:
NCT00101998
First received: January 18, 2005
Last updated: March 6, 2009
Last verified: March 2009

January 18, 2005
March 6, 2009
October 2003
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Change in weekly SCBM frequency. A SCBM is a spontaneous and complete bowel movement, which means a bowel movement that occurs with no laxative use in the prior 24 hours and leaves the subject with the feeling of complete evacuation of the rectum.
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Complete list of historical versions of study NCT00101998 on ClinicalTrials.gov Archive Site
Additional measures of Bowel movement (BM) frequency and symptoms, safety profile of the treatment regimens and any changes in pain intensity or opioid use.
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Study Of Alvimopan Drug For Treatment Of Constipation Due To Prescription Pain Medication
A Randomized, Double-Blind, Placebo-Controlled, Multicenter Phase IIb Study to Evaluate the Efficacy and Safety of Multiple Alvimopan Dosage Regimens for the Treatment of Opioid-Induced Bowel Dysfunction in Cancer Pain Subjects

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 subjects with cancer pain. The study will require five visits over a five-week period.

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Interventional
Phase 2
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double-Blind
Primary Purpose: Treatment
  • Constipation
  • Bowel Dysfunction
Drug: alvimopan
Other Name: alvimopan
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
215
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Inclusion criteria:

  • Subject is in any stage of cancer but has a minimum life expectancy of at least 3 months at the time of the Screening Visit.
  • Subject is taking opioid therapy for persistent cancer pain.
  • Subject meets the definition of opioid-induced bowel dysfunction as follows: Since starting opioid therapy, the subject has had decreased BM frequency and at least one of the following constipation symptoms [sensation of incomplete evacuation, difficulty in expelling stool (straining), hard stools (abnormal stool consistency)].
  • Subject understands the procedures, agrees to participate in the study, and has signed and dated the informed consent form prior to the initiation of any study-related activities, including discontinuation of pre-study laxative regimen or other prohibited medications.
  • Subject is able and willing to comply with a daily paper diary and is capable of completing paper questionnaires at study visits.

Exclusion criteria:

  • Subject is pregnant or lactating, or planning to become pregnant.
  • Subject is not ambulatory.
  • Subject has participated in another trial with an investigational drug (unapproved), device or procedure within 30 days of the Screening Visit.
  • Subject is unable to eat, drink, take/hold down oral medications.
  • Subject is taking opioids for the management of drug addiction.
  • Subject is unable or unwilling to discontinue the use of and/or refrain from using laxatives of all types and formulation at the Screening Visit and throughout the entire study.
  • Subject has severe constipation that has not been appropriately managed such that the subject is at immediate risk of developing serious complications of constipation. This would include a subject who has reported no bowel movement for 7 consecutive days prior to the Screening Visit.
  • Subject with gastrointestinal or pelvic disorders known to affect bowel transit, produce gastrointestinal (GI) obstruction, or contribute to bowel dysfunction.
  • Subject is currently taking vinca alkyloids or plans to take vinca alkyloids during the study.
  • Subject is currently undergoing abdominal radiation therapy and/or plans to undergo abdominal radiation therapy during the study.
  • Subject is HIV-infected, has active hepatitis (any subtype including ongoing chronic hepatitis B), or has ever been infected with hepatitis C.
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States,   Argentina,   Australia,   Canada,   Czech Republic,   Finland,   France,   Germany,   Hong Kong,   Hungary,   India,   Italy,   Korea, Republic of,   Netherlands,   New Zealand,   Pakistan,   Peru,   Philippines,   Poland,   Portugal,   Russian Federation,   South Africa,   Spain,   Taiwan,   Thailand,   United Kingdom
 
NCT00101998
767905/008
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Study Director, GSK
Cubist Pharmaceuticals
GlaxoSmithKline
Study Director: GSK Clinical Trials, MD GlaxoSmithKline
Cubist Pharmaceuticals
March 2009

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP