CClinicalTrials.gg
Status unknownNCT02666612Liquid BiopsyUpdated Jan 26, 2017

Measurement and Characterization of Circulating Endothelial Cells or Circulating Tumor Cells or Circulating DNA in Adult Patients With Metastatic Cancer

An interventional study of Blood samples in Metastatic Cancer, sponsored by Gustave Roussy, Cancer Campus, Grand Paris. Status unknown at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2017-01-26.

Sponsored by Gustave Roussy, Cancer Campus, Grand Paris · Not applicable, Interventional, and Diagnostic

The sponsor has not verified this record recently (last verified Jan 2017), so the status shown — last known as Recruiting — may be out of date.

From the registry’s dates

  • Registered 7 years after the study started (first participant enrolled Aug 2008, registered Aug 2015).
Phase
Not applicable
Study type
Interventional
Enrollment
2,240
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

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.

02

Conditions studied

03

In context

Neoplasm Metastasis

3,517 studies on the registry are indexed under Neoplasm Metastasis; 885 are open to participants now.

This study's planned enrollment of 2,240 is above the median of 54 across 2,767 interventional studies indexed under Neoplasm Metastasis.

Browse Neoplasm Metastasis studies →

Lead sponsor

Gustave Roussy, Cancer Campus, Grand Paris is the lead sponsor of 242 studies on the registry; 65 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Patients with metastatic solid tumor
  • Age> 18 years
  • Signed consent

Exclusion criteria

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.
05

Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
2,240 participants (estimated)

Study arms

  • Other
    Patients with metastatic cancer

    Procedure: Blood samples

Interventions

  • ProcedureBlood samples
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What researchers measure

Primary outcomes

  1. Measurement and characterization of CEC and CEP and circulaing DNA rate using flow cytometry

    Measurement and characterization of initial CEC and CEP circulaing DNA and their evolution under treatment

    Time frame: up to 2 years

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Study locations

1 of 1 sites recruiting
  • Gustave Roussy Cancer Campus Grand Paris
    Villejuif, Val de Marne 94805, France
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 26, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02666612
Lead sponsor
Gustave Roussy, Cancer Campus, Grand Paris
Responsible party
Sponsor
First posted
Jan 28, 2016
Start date
Aug 2008
Primary completion
Aug 2023 (estimated)
Completion
Aug 2023 (estimated)
Last update
Jan 26, 2017

Study contacts

Jean Charles Soria, MD-PhD
Contact
soria@gustaveroussy.fr
0142114291 ext. +33
Jean Charles Soria, MD-PhD
study chair · Gustave Roussy Cancer Campus

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jan 2017. You cannot join it, but the record below documents what was studied.

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