CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 70 enrolled
Drug / intervention
bevacizumab +5 morebiological
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/NCT00828009
NCT00828009Phase 2Completed

A Phase II Study of L-BLP25 and Bevacizumab in Unresectable Stage IIIA and IIIB Non-Squamous Non-Small Cell Lung Cancer After Definitive Chemoradiation

ECOG-ACRIN Cancer Research Group·interventional·Posted Jan 23, 2009·Updated Jul 7, 2023

In Brief

A Phase 2 clinical trial evaluating bevacizumab, Tecemotide, and 4 other interventions for Lung Cancer. Completed, enrolled 70 participants across 88 sites.

Detailed Summary

RATIONALE: Vaccines may help the body build an effective immune response to kill tumor cells. Monoclonal antibodies, such as bevacizumab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. Drugs used in chemotherapy work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Radiation therapy uses high-energy x-rays to kill tumor cells. Giving vaccine therapy together with bevacizumab after chemotherapy and radiation therapy may kill more tumor cells. PURPOSE: This phase II trial is studying the side effects of giving BLP25 liposome vaccine together with bevacizumab after chemotherapy and radiation therapy in treating patients with newly diagnosed stage IIIA or stage IIIB non-small cell lung cancer that cannot be removed by surgery.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsLung Cancer
CountriesUnited States

Timeline

Phase 2CompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
First PostedJan 23, 2009
Enrollment StartJan 17, 2011
Primary CompletionAug 20, 2018
Study CompletionMay 22, 2019
TodayJul 2, 2026
Enrollment to primary: 7.6 yearsPosted 17.4 years ago

Interventions

bevacizumabbiological

IV

Tecemotidebiological

carboplatindrug

IV

cyclophosphamidedrug

IV

paclitaxeldrug

IV

radiotherapyradiation

radiotherapy is given 5 days a week for 6½ weeks during concomitant chemoradiotherapy