Phase 3 Oesophageal Cancer Trial, Recruiting NCT06339060 Sponsor: Ruijin Hospital Condition: Oesophageal Cancer
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Phase 3 Oesophageal Cancer Trial, Recruiting

NCT06339060
Recruiting Phase 3

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 a specific type of oesophageal (food pipe) cancer called squamous cell carcinoma, confirmed by a tissue test, that is at a stage considered surgically removable and has not spread to distant parts of the body.
  • People whose general physical health and ability to carry out daily activities is rated at a good level (rated 0 or 1 on a standard medical scale).
  • People who have read, understood, and signed the official consent form for the study.

Who may not be able to join:

  • People who currently have, or have previously had, an autoimmune disease (a condition where the immune system attacks the body's own tissues).
  • People who require ongoing treatment with steroid medications or other medicines that suppress the immune system.
  • People who have a history of symptomatic interstitial lung disease (a type of long-term lung condition causing symptoms).
  • People who have a known allergy to any of the components of the study drug.
  • People who are pregnant or currently breastfeeding.
  • Men whose female partners are capable of becoming pregnant and who are not willing to use contraception during the study.
  • People who have previously received chemotherapy, radiation therapy, targeted therapy, or immunotherapy for this cancer or any previous cancer.
  • People with other medical conditions that, in the treating doctor's judgement, would make receiving the study drug unsafe or make it difficult to assess side effects (confirm with trial site).

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 3: approximately ~65% 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: Hecheng Li, MD/PHD, Ruijin Hospital Shanghaijiaotong University School of Medicine

Phone: 19121652450

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 3
Sponsor
Registry
ClinicalTrials.gov
Start date
1 May 2024
Est. completion
1 March 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

3-year overall survival rate

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