CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 275 enrolled
Drug / intervention
Docetaxel +3 moredrug
Likely dose
Docetaxel 40 mgfrom 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/NCT00499109
NCT00499109Phase 3Completed

Randomized Phase III Multicenter Trial of RRM1 & ERCC1 Directed Customized Chemotherapy Versus Standard of Care for 1st Line Treatment of Patients With Advanced Non-Small-Cell Lung Cancer

H. Lee Moffitt Cancer Center and Research Institute·interventional·Posted Jul 11, 2007·Updated Jul 9, 2014

In Brief

A Phase 3 clinical trial evaluating Docetaxel, Vinorelbine, and 2 other interventions for Non-Small Cell Lung Cancer. Completed, enrolled 275 participants across 9 sites in 3 countries.

Detailed Summary

This is a clinical research study to evaluate if chemotherapy in the experimental arm (E) results in a better outcome compared to patients in the standard of care arm (C). 2:1 randomization to experimental arm (E) or standard arm (C). In arm E, treatment of dual-agent chemotherapy will be selected based on RRM1 and ERCC1 expression at the protein level. In arm C, treatment of dual-agent chemotherapy will be gemcitabine/carboplatin, i.e., standard of care.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesGermany, Puerto Rico, United States
CollaboratorsSanofi

Timeline

Phase 3CompletedFinished
200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedJul 11, 2007
Enrollment StartMay 1, 2007
Primary CompletionApr 1, 2013
Study CompletionNov 1, 2013
TodayJul 2, 2026
Enrollment to primary: 5.9 yearsPosted 19.0 years ago

Interventions

Docetaxeldrug

GD Group: 40 mg/m\^2 on days 1 and 8, every 21 days DCb Group: 75 mg/m\^2 on day 1 DV Group: 50 mg/m\^2 on days 1 and 15, every 28 days

Vinorelbinedrug

DV Group: 35 mg/m\^2 on days 1 and 15

Carboplatindrug

GCb Group: Area under the curve (AUC) 5 on day 1, every 21 days DCb Group: AUC 6 on day 1, every 21 days Control Arm: Patients received up to 6 cycles, and no maintenance therapy was allowed.

Gemcitabinedrug

GCb Group: 1,250 mg/m\^2 on days 1 and 8 GD Group: 1,250 mg/m\^2 on days 1 and 8 Control Arm: Patients received up to 6 cycles, and no maintenance therapy was allowed.