Overview

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

Status:
Completed
Trial end date:
2006-05-01
Target enrollment:
0
Participant gender:
All
Summary
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.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Cubist Pharmaceuticals LLC
Collaborator:
GlaxoSmithKline
Treatments:
Alvimopan
Analgesics
Criteria
Inclusion criteria:

- Participant is in any stage of cancer but has a minimum life expectancy of at least 3
months at the time of the Screening Visit.

- Participant is taking opioid therapy for persistent cancer pain.

- Participant meets the definition of opioid-induced bowel dysfunction as follows: Since
starting opioid therapy, the subject has had decreased bowel movement (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)].

- Participant 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.

- Participant is able and willing to comply with a daily paper diary and is capable of
completing paper questionnaires at study visits.

Exclusion criteria:

- Participant is pregnant or lactating, or planning to become pregnant.

- Participant is not ambulatory.

- Participant has participated in another trial with an investigational drug
(unapproved), device or procedure within 30 days of the Screening Visit.

- Participant is unable to eat, drink, take/hold down oral medications.

- Participant is taking opioids for the management of drug addiction.

- Participant 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.

- Participant 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.

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

- Participant is currently taking vinca alkyloids or plans to take vinca alkyloids
during the study.

- Participant is currently undergoing abdominal radiation therapy and/or plans to
undergo abdominal radiation therapy during the study.

- Participant is human immunodeficiency virus (HIV)-infected, has active hepatitis (any
subtype including ongoing chronic hepatitis B), or has ever been infected with
hepatitis C.