drugset / Trial / NCT01523587

LUX-Lung 8: A Phase III Trial of Afatinib (BIBW 2992) Versus Erlotinib for the Treatment of Squamous Cell Lung Cancer After at Least One Prior Platinum Based Chemotherapy

NCT01523587 ↗

Phase 3 Completed 795 enrolled Boehringer Ingelheim
RandomizedParallel-groupOpen-labelTreatment

Summary

This randomised, open-label phase III trial will be performed in patients with advanced squamous cell carcinoma of the lung requiring second-line treatment after receiving first-line platinum-based chemotherapy. The primary objective of this trial is to compare the efficacy of BIBW 2992 to erlotinib as second-line treatment in this group of patients.

Timeline

Start
2012-03-05
Primary completion
2013-10-21
Completion
2017-12-27

Outcome

Met primary endpoint

registry analysis (superiority or other test); Afatinib vs Erlotinib; p = 0.0103; Hazard Ratio (HR) 0.814 (95% CI 0.693 to 0.956); NCT01523587 ↗

release “LUX-Lung 8 demonstrated that afatinib significantly reduced the risk of disease progression by 18%” prnewswire.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Afatinib Small molecule 40 mg Oral
Comparator Erlotinib Small molecule 150 mg Oral