Irinotecan in Treating Patients With Esophageal or Stomach Cancer
Part of paid clinical trials in Bakersfield, California.
- Sponsor
- Jonsson Comprehensive Cancer Center
- Study ID
- NCT00003748
- Phase
- PHASE2
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- irinotecan hydrochloride — DRUGOne course of therapy is comprised of a 4-week treatment period and a two-week rest period. Drug administration will be based on actual calculated body surface area. Starting dose will be 125 mg/m2/day given once per week on four consecutive weeks.
Study Details
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. PURPOSE: Phase II trial to study the effectiveness of irinotecan in treating patients who have esophageal or stomach cancer.
Key Dates
- Start date
- Aug 31, 1998
- Status verified
- Jul 2012
- Primary completion
- Jun 30, 2000
- Completion
- Jan 31, 2005
Study Design
- Enrollment
- 40 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: irinotecan hydrochlorideOne course of therapy is comprised of a 4-week treatment period and a two-week rest period. Drug administration will be based on actual calculated body surface area. Starting dose will be 125 mg/m2/day given once per week on four consecutive weeks.
Primary Outcome Measure
To determine the antitumor activity of irinotecan hydrochloride (CPT-11) in patients with unresectable adenocarcinoma of the esophagus and gastric cardia who have failed prior chemotherapy [ Time Frame: 2 years ]
Locations (25)
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Comprehensive Blood and Cancer Center· Bakersfield, CASt Jude Heritage Health Foundation· Fullerton, CADaniel Freeman Memorial Hospital· Inglewood, CAUCLA - Antelope Valley Cancer Center· Lancaster, CAPacific Shores Medical Group· Long Beach, CAJonsson Comprehensive Cancer Center, UCLA· Los Angeles, CA
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