CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 1,501 enrolled / 1,501 target
Drug / intervention
Bevacizumab +7 morebiological
Likely dose
30 mg/m2from 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/NCT00324805
NCT00324805Phase 3CompletedMonitor (6.6/mo)Completion was 128mo ago

A Phase III Randomized Trial of Adjuvant Chemotherapy With or Without Bevacizumab for Patients With Completely Resected Stage IB (≥ 4 cm) - IIIA Non-small Cell Lung Cancer (NSCLC)

National Cancer Institute (NCI)·interventional·Posted May 11, 2006·Updated Jun 23, 2026

In Brief

A Phase 3 clinical trial evaluating Bevacizumab, Cisplatin, and 6 other interventions for Stage IB Lung Non-Small Cell Carcinoma AJCC v7 and 3 related conditions. Completed, enrolled 1,501 participants across 1,169 sites in 5 countries.

Signals

Enrolling slower than its timeline implies

Detailed Summary

This randomized phase III trial studies chemotherapy and bevacizumab to see how well they work compared to chemotherapy alone in treating patients with stage IB, stage II, or stage IIIA non-small cell lung cancer that was removed by surgery. Drugs used in chemotherapy work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving more than one drug (combination chemotherapy) may kill more tumor cells. Monoclonal antibodies, such as bevacizumab, may interfere with the ability of tumor cells to grow and spread. Bevacizumab also may stop the growth of non-small cell lung cancer by blocking the growth of new blood vessels necessary for tumor growth. It is not yet known whether chemotherapy is more effective with or without bevacizumab in treating non-small cell lung cancer.

Study Details

Timeline

Phase 3CompletedFinished
2006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedMay 11, 2006
Enrollment StartJul 19, 2007
Primary CompletionOct 20, 2015
Study CompletionJan 31, 2025
TodayJul 2, 2026
Enrollment to primary: 8.3 yearsPosted 20.1 years ago

Arms & Interventions

Arm I (chemotherapy)active_comparator

Patients receive one of the following. For all, treatment repeats every 21 days for up to 4 courses in the absence of disease progression or unacceptable toxicity. REGIMEN 1: Vinorelbine ditartrate 30 mg/m2 IV on days 1 and 8, cisplatin 75 mg/m2 IV over 60 minutes on day 1 REGIMEN 2: Docetaxel 75 mg/m2 IV and cisplastin 75 mg/m2 IV on day 1 REGIMEN 3: Gemcitabine hydrochloride 1200 mg/m2 IV on days 1 and 8, cisplatin 75 mg/m2 IV on day 1 REGIMEN 4 (non-squamous histology only): Pemetrexed disodium 500mg/m2 IV and cisplatin 75 mg/m2 IV on day 1

Drug: CisplatinDrug: DocetaxelDrug: Gemcitabine HydrochlorideOther: Laboratory Biomarker AnalysisDrug: Pemetrexed DisodiumOther: Questionnaire AdministrationDrug: Vinorelbine Tartrate
Arm II (chemotherapy, bevacizumab)experimental

Patients receive chemotherapy as in Arm I. Patients also receive bevacizumab IV over 30-90 minutes on day 1. Treatment with bevacizumab repeats every 21 days for up to 1 year.

Biological: BevacizumabDrug: CisplatinDrug: DocetaxelDrug: Gemcitabine HydrochlorideOther: Laboratory Biomarker AnalysisDrug: Pemetrexed DisodiumOther: Questionnaire AdministrationDrug: Vinorelbine Tartrate

Interventions

Bevacizumabbiological

Given IV

Cisplatindrug

Given IV

Docetaxeldrug

Given IV

Gemcitabine Hydrochloridedrug

Given IV

Laboratory Biomarker Analysisother

Correlative studies

Pemetrexed Disodiumdrug

Given IV

Questionnaire Administrationother

Ancillary studies

Vinorelbine Tartratedrug

Given IV