Chemoembolization, Irinotecan Bead, Second Line Chemotherapy Treatment of Unresectable Metastatic Colorectal Cancer
Part of paid clinical trials in Aurora, Colorado.
- Sponsor
- Generic Devices Consulting, Inc.
- Study ID
- NCT00816777
- Phase
- PHASE1/PHASE2
- Status
- Terminated
Conditions
- Unresectable Metastatic Colo-rectal Cancer
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Chemoembolization with irinotecan Bead — PROCEDUREIntra arterial chemoembolization using Irinotecan Bead 100mg irinotecan per procedure in combination with irinotecan monotherapy 250mg/m2 alternating on a 3 weekly schedule
- Irinotecan — DRUGIrinotecan monotherapy: 250mg/m2 repeated every 3 weeks
Study Details
The primary objective of this study is to evaluate the safety and efficacy of Irinotecan Bead in combination with intravenous chemotherapy versus intravenous chemotherapy alone in the treatment of unresectable liver metastases in patients with colorectal cancer. The results of this study are intended to be used in support of a PMA application for a combination device
Key Dates
- Start date
- Dec 31, 2008
- Status verified
- Feb 2018
- Primary completion
- Jan 31, 2011
- Completion
- Mar 31, 2011
Study Design
- Enrollment
- 4 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: ChemoembolizationChemoembolization with Irinotecan Bead in combination with Intravenous Chemotherapy Group (test arm)
- Active Comparator: ChemotherapyIrinotecan monotherapy: 250mg/m2 repeated every 3 weeks
Primary Outcome Measure
Progression Free Survival [ Time Frame: 1 year ]
Locations (3)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Colorado Cancer Center | Aurora | Colorado | 80045 | - |
| Northwestern University | Chicago | Illinois | 60611 | - |
| Lahey Clinic | Burlington | Massachusetts | 01805 | - |