drugset / Trial / NCT02426125

A Study of Ramucirumab (LY3009806) Plus Docetaxel in Participants With Urothelial Cancer

NCT02426125 ↗

Phase 3 Completed 530 enrolled Eli Lilly and Company
RandomizedParallel-groupDouble-blindTreatment

Summary

The main purpose of this study is to evaluate the safety and efficacy of the study drug ramucirumab in combination with docetaxel in participants with urothelial cancer who failed prior platinum-based therapy.

Timeline

Start
2015-07-13
Primary completion
2017-04-21
Completion
2022-07-26

Outcome

Met primary endpoint

registry analysis (superiority test); Ramucirumab + Docetaxel vs Placebo + Docetaxel; p = 0.0118; Hazard Ratio (HR) 0.757 (95% CI 0.607 to 0.943); Log Rank; note: Stratified NCT02426125 ↗

release “RANGE is the first and only Phase 3 study of any therapy to show superior PFS over chemotherapy in a post-platinum setting in urothelial cancer.” lilly.com ↗

release “Phase 3 RANGE Study in Advanced or Metastatic Urothelial Cancer Significant improvement in primary endpoint of progression-free survival previously reported” lilly.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Ramucirumab Monoclonal antibody 10 mg/kg Intravenous
Background Docetaxel Small molecule 60 mg/m2 Intravenous
Background Docetaxel Small molecule 75 mg/m2 Intravenous

Indications