CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 530 enrolled
Drug / intervention
Ramucirumab +2 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

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

Search/NCT02426125
NCT02426125Phase 3Completed

A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study of Ramucirumab Plus Docetaxel Versus Placebo Plus Docetaxel in Patients With Locally Advanced or Unresectable or Metastatic Urothelial Carcinoma Who Progressed on or After Platinum-Based Therapy

Eli Lilly and Company·interventional·Posted Apr 24, 2015·Updated Aug 21, 2023

In Brief

A Phase 3 clinical trial evaluating Ramucirumab, Docetaxel, and 1 other intervention for Urothelial Carcinoma. Completed, enrolled 530 participants across 141 sites in 23 countries.

Detailed 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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesAustralia, Belgium, Canada, Denmark, France, Germany, Greece, Hungary, Israel, Italy, Japan, Mexico, Netherlands, Poland, Romania, Russia, South Korea, Spain, Taiwan, Turkey (Türkiye), Ukraine, United Kingdom, United States
Collaborators--

Timeline

Phase 3CompletedFinished
201520162017201820192020202120222023202420252026
First PostedApr 24, 2015
Enrollment StartJul 13, 2015
Primary CompletionApr 21, 2017
Study CompletionJul 26, 2022
TodayJul 2, 2026
Enrollment to primary: 1.8 yearsPosted 11.2 years ago

Interventions

Ramucirumabdrug

Administered IV

Docetaxeldrug

Administered IV

Placebodrug

Administered IV