CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 547 enrolled
Drug / intervention
Modified Bolus 5-FU/LV with Irinotecan +4 moredrug
Likely dose
Irinotecan 180 mg/m² IV over 90 minutes + Leucovorin 400 mg/m² IV over 2 hours + 5-FU 400 mg/m² IV bolus followed by 2400 mg/m² continuous infusion over 46 hours (FOLFIRI), repeated every 2 weeks; or Irinotecan 125 mg/m² IV on Days 1 & 8 + Leucovorin 20 mg/m² IV bolus + 5-FU 500 mg/m² IV bolus, repeated every 3 weeks; or Irinotecan 250 mg/m² IV + Capecitabine 1000 mg/m² PO BID Days 1-14, repeated every 3 weeks; with or without Bevacizumab 5-7.5 mg/kg IVAI-extracted
Key inclusion· 2
  • Histologically confirmed adenocarcinoma of colon or rectum with evidence of metastatic (Stage IV distant) disease
  • Primary lesion confirmed endoscopically, radiologically, or surgically to be in the large bowel
Key exclusion· 2
  • Any prior systemic anticancer therapy for metastatic colorectal cancer (chemotherapy, antibody therapy, immunotherapy, gene therapy, vaccine therapy, cytokine therapy, or experimental agents)
  • Concurrent malignancies at study entry, except early-stage prostate cancer, melanoma, bladder cancer, squamous/basal cell skin cancer, or in situ cervical cancer if effectively treated

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00101686
NCT00101686Phase 3Completed

A Randomized, Multi-Center Phase III Trial Of Irinotecan In Combination With Three Different Methods Of Administration Of Fluoropyrimidine: Infusional 5-FU (FOLFIRI), Modified-Bolus 5-FU (Day 1 & 8), And Oral Capecitabine (Day 1-14); With Celecoxib Versus Placebo As First-Line Treatment For Patients With Metastatic Colorectal Cancer Study Amended April 23, 2004 To Include Bevacizumab

Pfizer·interventional·Posted Jan 13, 2005·Updated Jan 12, 2010

In Brief

A Phase 3 clinical trial evaluating Modified Bolus 5-FU/LV with Irinotecan, FOLFIRI + bevacizumab, and 3 other interventions for Colorectal Neoplasms. Completed, enrolled 547 participants across 175 sites in 4 countries.

Detailed Summary

This study compares in the first study period combination of Irinotecan with three different methods of administration by Fluoropyrimidine. (ie. infusion, bolus and oral). In the second period of study it compares FOLFIRI \[a chemotherapy regime that combines bolus irinotecan and leucovorin \[LV\] with infusional 5-fluorouracil (5-FU)\] + bevacizumab and mlFL + bevacizumab. Measures of efficacy and safety will be reported.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesAustralia, Canada, New Zealand, United States
Collaborators--

Timeline

Phase 3CompletedFinished
2003200420052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedJan 13, 2005
Enrollment StartFeb 1, 2003
Primary CompletionOct 1, 2008
TodayJul 2, 2026
Enrollment to primary: 5.7 yearsPosted 21.5 years ago

Interventions

Modified Bolus 5-FU/LV with Irinotecandrug

Day 1 \& 8: Irinotecan (125 mg/m2 IV over 90 minutes), LV (20 mg/m2 IV bolus), 5-FU (500 mg/m2 IV bolus). All chemotherapy cycles repeated every 3 weeks. Celecoxib/placebo treatment will commence on the same day as chemotherapy treatment (i.e. Day 1 of treatment on study). Celecoxib/placebo will be taken at a dose of 400 mg po BID \[two times a day\] (800 mg/day) and will continue daily without interruption (no rest period for celecoxib/placebo treatment).

FOLFIRI + bevacizumabdrug

Day 1 Bevacizumab 5mg/kg IV 90 minutes prior to irinotecan/LV Irinotecan 180 mg/m2 IV 90 minutes Leucovorin 400 mg/m2 IV 2 hours - given with irinotecan without mixing. I m m e d i a t e l y f o l l o w e d b y : 5-FU 400 mg/m2 IV bolus 5-FU 2400 mg/m2 IV Continuous infusion over 46 hours Every 2 weeks Amendment 2 Bevacizumab 5mg/kg IV 90 minutes prior to irinotecan/LV Irinotecan 180 mg/m2 IV 90 minutes Leucovorin 400 mg/m2 IV 2 hours - given with irinotecan without mixing. I m m e d i a t e l y f o l l o w e d b y : 5-FU 400 mg/m2 IV bolus 5-FU 2400 mg/m2 IV Continuous infusion over 46 hours Celecoxib/placebo 400 mg BID \[two times a day\] oral Every 2 weeks

miFL + bevacizumabdrug

Day 1 Bevacizumab 7.5mg/kg IV \*over 90 minutes - given prior to irinotecan, 5-FU, and leucovorin Irinotecan 125 mg/m2 IV over 90 minutes Leucovorin 20 mg/m2 IV bolus 5-FU 500 mg/m2 IV bolus Day 8 Irinotecan 125 mg/m2 IV over 90 minutes Leucovorin 20 mg/m2 IV bolus 5-FU 500 mg/m2 IV bolus Every 3 weeks Amendment 2 Day 1 Bevacizumab 7.5mg/kg IV over 90 minutes - given prior to irinotecan, 5-FU, and leucovorin Irinotecan 125 mg/m2 IV over 90 minutes Leucovorin 20 mg/m2 IV bolus 5-FU 500 mg/m2 IV bolus Celecoxib/placebo 400 mg BID \[two times a day\] oral Day 8 Irinotecan 125 mg/m2 IV over 90 minutes Leucovorin 20 mg/m2 IV bolus 5-FU 500 mg/m2 IV bolus Celecoxib/placebo -- 400 mg po BID \[two times a day\] continues daily without interruption Every 3 weeks

Infusional 5-FU/LV with Irinotecandrug

Day 1: Irinotecan (180 mg/m2) IV over 90 minutes, LV (racemic mixture 400 mg/m2) over 2 hours during irinotecan infusion but without mixing, immediately followed by 5-FU IV bolus (400 mg/m2) and 5-FU continuous infusion (2400 mg/m2) over 46 hours. FOLFIRI regimen is repeated every 2 weeks. Celecoxib/placebo treatment will commence on the same day at a dose of 400 mg po BID \[two times a day\](800 mg/day) and will continue daily without interruption (no rest period for celecoxib/placebo treatment).

Oral Capecitabine with Irinotecandrug

Day 1: Irinotecan (250 mg/m2 IV) over 90 minutes; Day 1-14: capecitabine 1000 mg/m2 PO BID \[two times a day\] (28 single doses). All chemotherapy cycles repeated every 3 weeks. Celecoxib/placebo treatment will commence on the same day as chemotherapy treatment (i.e. Day 1 of treatment on study). Celecoxib/placebo will be taken at a dose of 400 mg po BID (800 mg/day) and will continue daily without interruption (no rest period for celecoxib/placebo treatment).