drugset / Trial / NCT00499109

Phase III of RRM1 & ERCC1 Directed Customized Chemotherapy for the Treatment of Patients With NSCLC

NCT00499109 ↗

RandomizedParallel-groupOpen-labelTreatment

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.

Timeline

Start
2007-05
Primary completion
2013-04
Completion
2013-11

Outcome

Missed primary endpoint

paper We found no statistically significant differences between the experimental arm and the control arm in PFS (6.1 months v 6.9 months) PMID 23690416 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Carboplatin Small molecule 5 unknown —
Subject Carboplatin Small molecule 6 unknown —
Subject Docetaxel Small molecule 40 mg/m2 —
Subject Docetaxel Small molecule 50 mg/m2 —
Subject Docetaxel Small molecule 75 mg/m2 —
Subject Gemcitabine Small molecule 1250 mg/m2 —
Subject Vinorelbine Small molecule 35 mg/m2 —