Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 2 Interventional Results available

A Safety and Efficacy Study of Carboplatin, Paclitaxel, Bevacizumab and CA4P in Non-Small Cell Lung Cancer

ClinicalTrials.gov ID: NCT00653939

Public ClinicalTrials.gov record NCT00653939. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 18, 2026, 2:08 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase II Study to Assess the Safety and Efficacy of the Combination of Carboplatin, Paclitaxel, and Bevacizumab ± Combretastatin A4 Phosphate (CA4P) Followed by Bevacizumab ± CA4P in Subjects With Chemotherapy Naïve Stage IIIB/IV Non-Squamous Cell Histology Non-Small Cell Lung Cancer (NSCLC)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to determine the safety, tolerability and efficacy of combretastatin A4 phosphate (CA4P), also known as fosbretabulin, in combination with bevacizumab (Avastin), carboplatin and paclitaxel in patients with chemotherapy naïve non-small cell lung cancer (NSCLC). This is a randomized parallel arm study. All participants will receive carboplatin, paclitaxel and bevacizumab, and half will additionally receive CA4P. Patients who complete the first 6 cycles of therapy and have not experienced disease progression will receive maintenance therapy with bevacizumab alone or with bevacizumab plus CA4P. The rationale for this study is the potential additive or synergistic actions of vascular disrupting agents like CA4P with anti-angiogenic agents like bevacizumab.

Study identification

NCT ID
NCT00653939
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Mateon Therapeutics
Industry
Enrollment
63 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 2008 (Type not available)
Primary completion
Jul 2011 (Actual)
Completion
Oct 2011 (Actual)
Last update posted
Feb 9, 2015

2008 – 2011

United States locations

U.S. sites
15
U.S. states
10
U.S. cities
15
Facility City State ZIP Site status
Southbay Oncology Hematology Campbell California 95008 —
Pacific Coast Hematology and Oncology Medical Group Fountain Valley California 92708 —
UCLA Division of Hematology and Oncology Los Angeles California 90095 —
Bay Area Cancer Research Group, LLC Pleasant Hill California 94523 —
Boca Raton Comprehensive Cancer Center Boca Raton Florida 21020 —
Kentuckiana Cancer Institute Louisville Kentucky 40202 —
Lahey Clinic Medical Center Burlington Massachusetts 01805 —
The Center for Cancer and Hematologic Disease Cherry Hill New Jersey 08003 —
San Juan Oncology Associates Farmington New Mexico 87401 —
Gabrail Cancer Center Canton Ohio 44718 —
The Mark H. Zangmeister Center Columbus Ohio 43219 —
Signal Point Clinical Research Middletown Ohio 45042 —
Blueridge Cancer Care Salem Virginia 24153 —
Northwest Medical Specialties Tacoma Washington 98405 —
Mary Babb Randolph Cancer Center-Clinical Trials Unit Morgantown West Virginia 26506 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00653939, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 9, 2015 · Synced Oct 18, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00653939 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →