NCT01891708

Brief Summary

a. VEGFRs may be the biomarker which can predict the effect of bevacizumab in non small cell lung cancer

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
40

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Jun 2013

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 1, 2013

Completed
18 days until next milestone

First Submitted

Initial submission to the registry

June 19, 2013

Completed
14 days until next milestone

First Posted

Study publicly available on registry

July 3, 2013

Completed
1.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2014

Completed
4 years until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2018

Completed
Last Updated

July 3, 2013

Status Verified

July 1, 2013

Enrollment Period

1.5 years

First QC Date

June 19, 2013

Last Update Submit

July 2, 2013

Conditions

Outcome Measures

Primary Outcomes (1)

  • PFS

    6 months

Secondary Outcomes (1)

  • OS

    18 months

Interventions

the dose and application model of the three intervention are not specified by the sponsor who just observe the efficacy of the combination application of the three in non small cell lung cancer patients with brain metastasis once enrolled.

Also known as: Drug:bevacizumab,also Avastine, Drug:standard chemotherapy recommended by clinical guidlines, Radiation

Eligibility Criteria

Age18 Years - 75 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

advanced non small cell lung cancer patients with brain metastatic disease

You may qualify if:

  • non squamous cell non small cell lung cancer
  • with measurable disease
  • ECOG 0-1

You may not qualify if:

  • \- patients received surgery in recent 4 weeks

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Cancer Center, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

Wuhan, Hubei, 430071, China

RECRUITING

Biospecimen

Retention: SAMPLES WITHOUT DNA

peripheral blood

MeSH Terms

Conditions

Carcinoma, Non-Small-Cell LungBrain Neoplasms

Interventions

BevacizumabRadiation

Condition Hierarchy (Ancestors)

Carcinoma, BronchogenicBronchial NeoplasmsLung NeoplasmsRespiratory Tract NeoplasmsThoracic NeoplasmsNeoplasms by SiteNeoplasmsLung DiseasesRespiratory Tract DiseasesCentral Nervous System NeoplasmsNervous System NeoplasmsBrain DiseasesCentral Nervous System DiseasesNervous System Diseases

Intervention Hierarchy (Ancestors)

Antibodies, Monoclonal, HumanizedAntibodies, MonoclonalAntibodiesImmunoglobulinsImmunoproteinsBlood ProteinsProteinsAmino Acids, Peptides, and ProteinsSerum GlobulinsGlobulinsPhysical Phenomena

Study Officials

  • Li Liu, MD

    Cancer Center, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
PROSPECTIVE
Target Duration
2 Months
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

June 19, 2013

First Posted

July 3, 2013

Study Start

June 1, 2013

Primary Completion

December 1, 2014

Study Completion

December 1, 2018

Last Updated

July 3, 2013

Record last verified: 2013-07

Locations