CI

At a glance

ClinicalIndex Comparison Record
Phase 2Active· 5 enrolled / 5 target
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/NCT02971501
NCT02971501Phase 2ActiveUpdate Overdue (0.1/mo)Completion was 16mo ago

A Phase II Trial of Osimertinib (AZD9291) With or Without Bevacizumab in Patients With EGFR Mutation Positive NSCLC and Brain Metastases

National Cancer Institute (NCI)·interventional·Posted Nov 23, 2016·Updated Jun 26, 2026

In Brief

A Phase 2 clinical trial evaluating Bevacizumab, Biopsy Procedure, and 4 other interventions for Metastatic Lung Non-Small Cell Carcinoma and 2 related conditions. Active but no longer recruiting, targeting 5 participants across 18 sites.

Signals

Enrollment appears stalled

Detailed Summary

This phase II trial studies how well osimertinib with or without bevacizumab works in treating patients with EGFR positive non-small cell lung cancer that has spread to the brain (brain metastases). Osimertinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Bevacizumab may stop or slow non-small cell lung cancer by blocking the growth of new blood vessels necessary for tumor growth. Giving osimertinib with or without bevacizumab may work better in treating patients with non-small cell lung cancer.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2ActiveOverdue
2017201820192020202120222023202420252026
First PostedNov 23, 2016
Enrollment StartJun 27, 2018
Primary CompletionFeb 18, 2025
Study CompletionJul 1, 2026
TodayJul 2, 2026
Enrollment to primary: 6.6 yearsPosted 9.6 years ago

Arms & Interventions

Arm I (osimertinib, bevacizumab)experimental

Patients receive osimertinib PO QD on days 1-21 and bevacizumab IV over 30-90 minutes on day 1. Cycles repeat every 21 days in the absence of disease progression or unacceptable toxicity. Patients undergo CT scan, MRI, tumor biopsy and blood sample collection throughout the study.

Biological: BevacizumabProcedure: Biopsy ProcedureProcedure: Biospecimen CollectionProcedure: Computed TomographyProcedure: Magnetic Resonance ImagingDrug: Osimertinib
Arm II (osimertinib)experimental

Patients receive osimertinib PO QD on days 1-21. Cycles repeat every 21 days in the absence of disease progression or unacceptable toxicity. Patients undergo CT scan, MRI, tumor biopsy and blood sample collection throughout the study.

Drug: Osimertinib

Interventions

Bevacizumabbiological

Given IV

Biopsy Procedureprocedure

Undergo tumor biopsy

Biospecimen Collectionprocedure

Undergo blood sample collection

Computed Tomographyprocedure

Undergo CT scan

Magnetic Resonance Imagingprocedure

Undergo MRI

Osimertinibdrug

Given PO