CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 795 enrolled
Drug / intervention
afatinib +1 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/NCT01523587
NCT01523587Phase 3Completed

LUX-Lung 8: A Randomized, Open-label Phase III Trial of Afatinib Versus Erlotinib in Patients With Advanced Squamous Cell Carcinoma of the Lung as Second-line Therapy Following First-line Platinum-based Chemotherapy

Boehringer Ingelheim·interventional·Posted Feb 1, 2012·Updated Feb 15, 2019

In Brief

A Phase 3 clinical trial evaluating afatinib and erlotinib for Carcinoma, Non-Small-Cell Lung. Completed, enrolled 795 participants across 192 sites in 23 countries.

Detailed 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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesArgentina, Austria, Canada, Chile, China, Denmark, France, Germany, Greece, Hungary, India, Ireland, Italy, Mexico, Netherlands, Portugal, Singapore, South Korea, Spain, Taiwan, Turkey (Türkiye), United Kingdom, United States
Collaborators--

Timeline

Phase 3CompletedFinished
201220132014201520162017201820192020202120222023202420252026
First PostedFeb 1, 2012
Enrollment StartMar 5, 2012
Primary CompletionOct 21, 2013
Study CompletionDec 27, 2017
TodayJul 2, 2026
Enrollment to primary: 1.6 yearsPosted 14.4 years ago

Interventions

afatinibdrug

Afatinib taken once daily, continuously until disease progression or unacceptable toxicity.

erlotinibdrug

erlotinib taken once daily