drugset / Trial / NCT00364013

PRIME: Panitumumab Randomized Trial In Combination With Chemotherapy for Metastatic Colorectal Cancer to Determine Efficacy

NCT00364013 ↗

Phase 3 Completed 1183 enrolled Amgen
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the treatment effect of panitumumab in combination with FOLFOX compared to FOLFOX alone as first line therapy for metastatic colorectal cancer

Timeline

Start
2006-08-01
Primary completion
2009-08-01
Completion
2013-03-22

Outcome

Met primary endpoint

registry MEDIAN Wild-type KRAS - FOLFOX + Panitumumab: 9.6 (9.2 to 11.1) months NCT00364013 ↗

registry analysis (unspecified test); Wild-type KRAS - FOLFOX + Panitumumab vs Wild-type KRAS - FOLFOX; p = 0.0234; Normal score -2.27; Stratified log-rank test; NCT00364013 ↗

release “The PRIME study showed that patients with wild-type KRAS tumors (exon 2) achieved statistically significant improvement in PFS with Vectibix and FOLFOX versus FOLFOX alone” amgen.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Panitumumab Monoclonal antibody 6 mg/kg —
Background Leucovorin Small molecule 200 mg/m2 —
Background Oxaliplatin Small molecule 85 mg/m2 —
Background fluorouracil Small molecule 400 mg/m2 —
Background fluorouracil Small molecule 600 mg/m2 —

Indications