CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 399 enrolled
Drug / intervention
Icotinib +1 moredrug
Likely dose
Icotinib 125 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/NCT01040780
NCT01040780Phase 3Completed

A Randomized,Double-blind,Multicenter Phase III Trial to Evaluate the Safety and Efficacy of Icotinib and Gefitinib in Advanced NSCLC Patients Previously Treated With Chemotherapy

Betta Pharmaceuticals Co., Ltd.·interventional·Posted Dec 30, 2009·Updated Feb 14, 2014

In Brief

A Phase 3 clinical trial evaluating Icotinib and Gefitinib for Non-small Cell Lung Cancer. Completed, enrolled 399 participants across 27 sites.

Detailed Summary

The purpose of this study is to determine whether Icotinib is at least non-inferior to Gefitinib in the treatment of advanced non-small cell lung cancer (NSCLC) patients after one or two chemotherapies.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesChina
Collaborators--

Timeline

Phase 3CompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
First PostedDec 30, 2009
Enrollment StartFeb 1, 2009
Primary CompletionMar 1, 2010
Study CompletionDec 1, 2011
TodayJul 1, 2026
Enrollment to primary: 1.1 yearsPosted 16.5 years ago

Interventions

Icotinibdrug

125 mg three times daily (375 mg per day) by mouth

Gefitinibdrug

250 mg every 24 hours by mouth