Phase 2 Oesophageal Cancer Trial, Recruiting NCT06187597 Sponsor: Sun Yat-sen University Condition: Oesophageal Cancer
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Phase 2 Oesophageal Cancer Trial, Recruiting

NCT06187597
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:

  • People who have been diagnosed with squamous cell carcinoma (a specific type of cancer) of the esophagus (food pipe), confirmed by a tissue biopsy.
  • People whose cancer is locally advanced (has grown in the area around the esophagus) but has not spread through the bloodstream to other parts of the body.
  • People whose cancer has been assessed as not suitable for surgery, either for medical reasons or because surgery is not the person's choice.
  • People who were aged between 70 and 85 years old at the time of their cancer diagnosis.
  • People who have not previously received any cancer treatment.
  • People with an estimated life expectancy of more than 6 months.
  • People who are reasonably functional in daily life — specifically, those with an ECOG performance score of 2 or lower, meaning they may have some symptoms but are able to care for themselves (confirm with trial site for exact definition).
  • People with no history of any other cancer, past or current.
  • People whose blood, liver, and kidney test results meet specific minimum levels required by the trial (confirm with trial site for exact values).
  • People who are able to understand the study and agree to participate by signing a consent form.

Who may not be able to join:

  • People who have already received any form of cancer treatment, including chemotherapy, radiotherapy, surgery, or immunotherapy.
  • People whose cancer has already spread through the bloodstream to other parts of the body, or who have an esophageal fistula (an abnormal opening in the food pipe) at the time of diagnosis.
  • People with a known or suspected allergy or sensitivity to monoclonal antibody medicines, to the study drug cadonilimab, or to the chemotherapy drugs paclitaxel or cisplatin.
  • People who have a pre-existing or current bleeding disorder.
  • People who are unable to give informed consent due to psychological, family, social, or other personal circumstances.
  • People who have moderate or severe peripheral neuropathy (nerve damage causing numbness, tingling, or weakness, typically in the hands or feet) — specifically, grade 2 or higher (confirm with trial site).
  • People with a history of any other cancer before enrolling in the trial, with the exception of certain non-serious skin cancers, cervical cancer that had not spread, or prostate cancer that was fully cured.
  • People who have had diabetes for more than 10 years and whose blood sugar levels are poorly controlled.
  • People who cannot tolerate chemotherapy and radiation treatment due to serious heart, lung, liver, or kidney problems, blood disorders, or severe malnutrition (cachexia).
  • People with active autoimmune diseases (where the immune system attacks the body), a history of autoimmune conditions (such as colitis, hepatitis, or an overactive thyroid), a weakened immune system including HIV, or a history of organ or bone marrow transplant.
  • People with a history of interstitial lung disease or non-infectious pneumonia (a type of lung inflammation not caused by infection).
  • People who have had active tuberculosis (TB) in the lung within the past year, or who had active lung TB more than a year ago but did not complete proper TB treatment.
  • People with currently active hepatitis B or hepatitis C infections at levels above the thresholds set by the trial (confirm with trial site for exact values).

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 14 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

Principal Investigator: Mian Xi, MD, Sun Yat-sen University

Phone: 862087343385

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
1 March 2024
Est. completion
31 December 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Progression-free survival

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: 14 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