Phase 2 Oesophageal Cancer Trial, Recruiting NCT07205731 Sponsor: University Hospital, Clermont-Ferrand Condition: Oesophageal Cancer
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Phase 2 Oesophageal Cancer Trial, Recruiting

NCT07205731
Recruiting Phase 2

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:

  • You have been confirmed by a tissue biopsy to have a type of esophageal (food pipe) cancer called squamous cell carcinoma
  • Your cancer has spread to other parts of the body or is at an advanced local stage
  • You have not yet received any treatment (such as immunotherapy, chemotherapy, or radiotherapy) for this stage of your cancer
  • Your cancer specialist and a doctor specialising in older adult care have decided that standard platinum-based chemotherapy is not suitable for you
  • You have at least one tumour that can be measured or evaluated on a scan
  • You are 70 years of age or older
  • You are still able to carry out some daily activities (your general health and functioning level meets a specific medical standard — confirm with trial site)
  • Your life expectancy is estimated to be more than 3 months
  • If you had previous treatment after surgery (adjuvant therapy), it was completed more than 6 months ago
  • Your blood counts and organ function (bone marrow, liver, kidneys) are at an acceptable level as shown by recent blood tests
  • If you are male and sexually active, you are willing to use a condom during treatment and for 6 months after the last dose, particularly with a pregnant partner or a partner who could become pregnant; female partners should also use effective contraception during this period
  • You are willing and able to attend all required appointments, treatments, and follow-up visits as set out in the study plan
  • You have signed a consent form agreeing to take part before any study-related procedures begin
  • You are covered by a social security (health insurance) scheme

Who may not be able to join:

  • You have a history of another cancer, unless it was fully treated with no signs of return for at least 2 years, or it was a minor skin cancer or early-stage cancer (carcinoma in situ) that has been fully treated with no signs of disease
  • Your esophageal cancer is at a stage where surgery or curative radiotherapy may still be possible, according to the local specialist
  • You have taken part in another clinical trial involving an experimental treatment in the last 2 months
  • You are currently enrolled in another clinical trial that involves an active treatment (observational studies or follow-up phases may be allowed — confirm with trial site)
  • You have previously had an organ transplant, bone marrow transplant, or umbilical cord blood transplant from another person
  • You have an active autoimmune or inflammatory condition (such as Crohn's disease, lupus, rheumatoid arthritis, or similar conditions) — although some milder conditions such as well-controlled thyroid disease, vitiligo, hair loss, or diet-controlled celiac disease may still be eligible (confirm with trial site)
  • You have previously received immunotherapy drugs that target immune checkpoints within the last 2 years
  • You have an uncontrolled or serious illness, including uncontrolled fluid build-up around the lungs, heart, or abdomen that needs frequent draining
  • You have a connection (fistula) between your food pipe and your airway or main blood vessel (aorta)
  • You have had a serious heart event such as a heart attack, blood clot, stroke, or heart failure within the last 6 months, or have other uncontrolled serious medical conditions
  • You have a blood or bone marrow disorder called myelodysplastic syndrome or acute myeloid leukaemia, or show signs that may suggest these conditions
  • You have cancer that has spread to your brain and is causing symptoms
  • You have a primary immune deficiency condition
  • You have HIV that is not well controlled, with a low immune cell count (confirm with trial site)
  • You have an active infection, including active tuberculosis, untreated hepatitis B, or active hepatitis C
  • You have taken immune-suppressing medication in the 14 days before starting the study treatment (with some exceptions, such as low-dose steroids, inhaled or topical steroids — confirm with trial site)
  • You have received a live vaccine within 30 days before starting the study immunotherapy
  • You are unable or unlikely to attend follow-up appointments, for any reason including personal, family, psychological, or geographical circumstances
  • You are legally deprived of freedom, under certain forms of psychiatric care orders, or are legally unable to give your own consent to participate

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 27 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Phone: 0473754963

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
Phase 2
Registry
ClinicalTrials.gov
Start date
7 October 2025
Est. completion
1 October 2029

Where this trial is recruiting

🇫🇷 France

Primary endpoints

To assess the percentage of patients alive at 6 months in elderly patients, not eligible to platinum-based chemotherapy, treated by anti-PD1 Tislelizumab alone as first-line treatment for an advanced ESCC

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: 27 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