Pancreatic Cancer Trial, Recruiting NCT06046794 Sponsor: Institut Paoli-Calmettes Condition: Pancreatic Cancer
Back to Pancreatic Cancer

Pancreatic Cancer Trial, Recruiting

NCT06046794
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 who have been diagnosed with metastatic pancreatic cancer (a type of cancer that has spread beyond the pancreas), confirmed by a tissue test.
  • People who are not able to receive a chemotherapy combination called FOLFIRINOX and are about to start first-line treatment with a single chemotherapy drug called gemcitabine.
  • People whose stored tumour tissue sample meets certain quality requirements needed for a specific test used in this trial (confirm with trial site).
  • People with a life expectancy of more than 2 months.
  • People whose cancer can be measured on scans using a standard set of measurement rules called RECIST 1.1.
  • People who have not previously received any treatment for their cancer after it spread (metastatic stage).
  • People aged 18 years or older.
  • People who do not object to taking part in the study.
  • People who are members of, or covered by, a social security or health insurance scheme (this appears to be a French healthcare requirement — confirm with trial site).

Who may not be able to join:

  • People for whom gemcitabine chemotherapy is medically unsuitable or unsafe.
  • People whose general health and ability to carry out daily activities falls below a certain level, as measured by a standard medical scale (confirm with trial site).
  • People who are in an emergency situation or are unable to indicate whether they object to taking part.
  • People who are under a legal protection order, such as guardianship or a similar arrangement.
  • People who are unable to attend regular medical follow-up appointments due to geographic, social, or psychological reasons.

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 26 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

Phone: 0491223778

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
Institut Paoli-Calmettes
Registry
ClinicalTrials.gov
Start date
23 May 2024
Est. completion
1 November 2027

Where this trial is recruiting

🇫🇷 France

Primary endpoints

Percentage of alive GemCore+ patients treated with Gemcitabine

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: 26 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