- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02666612
Measurement and Characterization of Circulating Endothelial Cells or Circulating Tumor Cells or Circulating DNA in Adult Patients With Metastatic Cancer (Liquid Biopsy)
January 25, 2017 updated by: Gustave Roussy, Cancer Campus, Grand Paris
Monitoring of circulating endothelial cells (CEC and mature cells called progenitors called CEP) or circulating tumor cells (CTC) in adult patients with metastatic cancer, possibly treated with targeted therapy.
Study Overview
Study Type
Interventional
Enrollment (Anticipated)
2240
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Jean Charles Soria, MD-PhD
- Phone Number: +33 0142114291
- Email: soria@gustaveroussy.fr
Study Locations
-
-
Val de Marne
-
Villejuif, Val de Marne, France, 94805
- Recruiting
- Gustave Roussy Cancer Campus Grand Paris
-
Contact:
- Jean Charles Soria, MD-PhD
- Phone Number: +33 0142114291
- Email: soria@gustaveroussy.fr
-
-
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 and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Patients with metastatic solid tumor
- Age> 18 years
- Signed consent
Exclusion Criteria:
- Patients with diseases associated with vascular lesions known.
- Patients protected by law, in accordance with Articles L1121-5 to L1121-8 of the Code of Public Health.
- Mental pathology that can interfere with the proper conduct of the study.
- Refusal of consent.
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
- Primary Purpose: Diagnostic
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Other: Patients with metastatic cancer
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Measurement and characterization of CEC and CEP and circulaing DNA rate using flow cytometry
Time Frame: up to 2 years
|
Measurement and characterization of initial CEC and CEP circulaing DNA and their evolution under treatment
|
up to 2 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Chair: Jean Charles Soria, MD-PhD, Gustave Roussy Cancer Campus
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 (Actual)
August 1, 2008
Primary Completion (Anticipated)
August 1, 2023
Study Completion (Anticipated)
August 1, 2023
Study Registration Dates
First Submitted
August 12, 2015
First Submitted That Met QC Criteria
January 27, 2016
First Posted (Estimate)
January 28, 2016
Study Record Updates
Last Update Posted (Estimate)
January 26, 2017
Last Update Submitted That Met QC Criteria
January 25, 2017
Last Verified
January 1, 2017
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2008-A00585-50
- 2008/1370 (Other Identifier: CSET number)
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.
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