- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01891708
VEGFRs Predict Bevacizumab Benefit in Advanced Non Small Cell Lung Cancer
July 2, 2013 updated by: Li Liu
a. VEGFRs may be the biomarker which can predict the effect of bevacizumab in non small cell lung cancer
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
- non small cell lung cancer (non squamous carcinoma)
- ECOG 0-1
- from 18-75 years old
Study Type
Observational
Enrollment (Anticipated)
40
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Hubei
-
Wuhan, Hubei, China, 430071
- Recruiting
- Cancer Center, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
-
Contact:
- Li Liu, MD
- Phone Number: 027-85872015
- Email: liulixiehe@163.com
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 75 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
advanced non small cell lung cancer patients with brain metastatic disease
Description
Inclusion Criteria:
- non squamous cell non small cell lung cancer
- with measurable disease
- ECOG 0-1
Exclusion Criteria:
- patients received surgery in recent 4 weeks
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Case-Only
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
PFS
Time Frame: 6 months
|
6 months
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
OS
Time Frame: 18 months
|
18 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Li Liu, MD, Cancer Center, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
June 1, 2013
Primary Completion (Anticipated)
December 1, 2014
Study Completion (Anticipated)
December 1, 2018
Study Registration Dates
First Submitted
June 19, 2013
First Submitted That Met QC Criteria
July 2, 2013
First Posted (Estimate)
July 3, 2013
Study Record Updates
Last Update Posted (Estimate)
July 3, 2013
Last Update Submitted That Met QC Criteria
July 2, 2013
Last Verified
July 1, 2013
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Brain Diseases
- Central Nervous System Diseases
- Nervous System Diseases
- Respiratory Tract Diseases
- Neoplasms
- Lung Diseases
- Neoplasms by Site
- Respiratory Tract Neoplasms
- Thoracic Neoplasms
- Carcinoma, Bronchogenic
- Bronchial Neoplasms
- Central Nervous System Neoplasms
- Nervous System Neoplasms
- Lung Neoplasms
- Carcinoma, Non-Small-Cell Lung
- Brain Neoplasms
- Physiological Effects of Drugs
- Antineoplastic Agents
- Antineoplastic Agents, Immunological
- Angiogenesis Inhibitors
- Angiogenesis Modulating Agents
- Growth Substances
- Growth Inhibitors
- Bevacizumab
Other Study ID Numbers
- XHZL02
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.