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Discovery of Microbiome-based Biomarkers for Patients With Cancer Using Metagenomic Approach

Discovery of Microbiome-based Biomarkers for Patients With Cancer Using Metagenomic Approach

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Phase N/A

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Overview

Multicentric prospective study with collection of biological samples as part of type II research

Eligibility

Inclusion Criteria:

  • Patient with cancer who will start treatment anticancer (see cohorts).
  • Patient information and signature of the consent form before any specific procedure for the study. The patient must be able and must be inclined to cooperate in the study procedures.
  • Patient affiliated to a social security scheme or beneficiary of a similar scheme.

Exclusion Criteria:

  • Pregnant or lactating woman
  • Patient under guardianship or curatorship or deprived of liberty by a decision judicial or administrative or patient unable to give his consent.

Study details
    Cancer

NCT04567446

Gustave Roussy, Cancer Campus, Grand Paris

15 May 2026

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FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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