Colorectal Cancer Trial, Recruiting NCT03841799 Sponsor: Centre Leon Berard Condition: Colorectal Cancer
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Colorectal Cancer Trial, Recruiting

NCT03841799
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People aged 18 or older at the time of signing the consent form
  • People in Cohort A: those with a benign or cancerous colorectal (bowel) growth (ranging from early to moderate stage) who are suitable for surgery, and who have not previously received any cancer-fighting medications or radiation therapy
  • People in Cohort B: those with a localised cancer of the colon or rectum who are suitable for surgery and who have already been treated with radiation therapy and/or pre-operative chemotherapy
  • People who are able and willing to follow all the procedures required by the trial
  • People who understand and voluntarily sign and date the consent form before any trial-related procedures begin
  • People who have active medical insurance coverage

Who may not be able to join:

  • People who are pregnant or currently breastfeeding
  • People who have received immune-affecting medications (such as steroids or immunosuppressive treatments) within the 4 weeks before joining, or antibiotics within the 8 weeks before joining
  • People who have, or have had, another type of cancer — unless that cancer is not expected to affect the trial results and the trial sponsor approves it (for example, certain treated skin cancers or cervical in-situ carcinoma may be acceptable; people previously treated for another cancer with no sign of return for at least 1 year may still be considered — confirm with trial site)
  • People who have an inflammatory condition or an autoimmune disease
  • People who are under legal guardianship, court-ordered protection, or similar legal arrangements

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 20 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Matthieu SARABI, Dr, Centre Leon Berard

Phone: 04 26 55 68 24

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Centre Leon Berard
Registry
ClinicalTrials.gov
Start date
2 May 2019
Est. completion
1 December 2027

Where this trial is recruiting

🇫🇷 France

Primary endpoints

Characterization of colorectal tissue microenvironment of patients with locally colorectal neoplasia.

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 20 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov