CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 540 enrolled
Drug / intervention
Eribulin +1 moredrug
Likely dose
Eribulin 1.4 mg/m2from 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/NCT01454934
NCT01454934Phase 3Completed

A Randomized, Open-label, Multicenter, Phase 3 Study to Compare the Efficacy and Safety of Eribulin With Treatment of Physician's Choice in Subjects With Advanced Non-Small Cell Lung Cancer

Eisai Inc.·interventional·Posted Oct 19, 2011·Updated Jun 22, 2023

In Brief

A Phase 3 clinical trial evaluating Eribulin and TPC -Vinorelbine,Gemcitabine,Docetaxel, and Pemetrexed for Non-Small Cell Lung Cancer (NSCLC). Completed, enrolled 540 participants across 83 sites in 14 countries.

Detailed Summary

This is a randomized, open-label, multicenter, Phase 3 study, comparing efficacy and safety of eribulin with TPC in subjects with advanced and disease progression following at least two prior regimens for advanced disease, which should have included a platinum-based regimen.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesAustralia, France, Germany, Hong Kong, Italy, Japan, Poland, Russia, Singapore, South Korea, Spain, Taiwan, United Kingdom, United States
Collaborators--

Timeline

Phase 3CompletedFinished
201220132014201520162017201820192020202120222023202420252026
First PostedOct 19, 2011
Enrollment StartDec 9, 2011
Primary CompletionMay 30, 2014
Study CompletionMay 2, 2016
TodayJul 2, 2026
Enrollment to primary: 2.5 yearsPosted 14.7 years ago

Interventions

Eribulindrug

Administration of eribulin mesylate at a dose of 1.4 mg/m2 i.v. over 2 to 5 minutes on Days 1 and Day 8 of every cycle, where the duration of each cycle is 21 days.

TPC -Vinorelbine,Gemcitabine,Docetaxel, and Pemetrexeddrug

* Vinorelbine 30 mg/m2 i.v. on Day 1, every 7 days * Gemcitabine 1250 mg/m2 i.v. on Days 1 and 8, every 21 days * Docetaxel 75 mg/m2 i.v. on Day 1 every 21 days * Pemetrexed 500 mg/m2 i.v. on Day 1 every 21 days (nonsquamous histology only).