Phase 3 Oesophageal Cancer Trial, Recruiting NCT04807673 Sponsor: Tianjin Medical University Cancer Institute and Hospital Condition: Oesophageal Cancer
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Phase 3 Oesophageal Cancer Trial, Recruiting

NCT04807673
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 esophageal squamous cell carcinoma (a specific type of oesophageal cancer) confirmed by a tissue test
  • People whose cancer is located in the chest portion of the oesophagus, has not spread to distant parts of the body, and is considered suitable for complete surgical removal based on specific staging criteria (confirm with trial site)
  • People with no signs of cancer spread to the lymph nodes near the collarbone
  • People who are fully active or have only minor restrictions on physical activity, as measured by a standard medical scale (ECOG score of 0 or 1)
  • People aged 18 to 75 years, of any gender
  • People who are willing and able to sign a written consent form for the trial
  • People whose liver, kidneys, and other organs are functioning well enough to participate (confirm with trial site)
  • Women who could become pregnant must have a negative pregnancy test taken within 72 hours before the first treatment dose
  • People who are willing to provide tissue, blood, and urine samples, including a fresh tissue sample taken within 28 days before treatment begins
  • People who have not previously received any systemic or local treatment for oesophageal cancer

Who may not be able to join:

  • People for whom oesophageal surgery is not medically suitable or is otherwise not recommended
  • People who have previously had surgery, radiotherapy, immunotherapy, or chemotherapy for oesophageal cancer
  • People who currently have, or have a history of, an autoimmune disease
  • People who require ongoing treatment with steroid medications or other drugs that suppress the immune system
  • People who have a history of symptomatic interstitial lung disease (a condition causing scarring or inflammation in the lungs)
  • People who have a known allergy to any components of the study drug
  • People who are currently pregnant or breastfeeding
  • People who have previously received chemotherapy, radiotherapy, targeted therapy, or immunotherapy for this cancer or any other past cancer
  • People with other underlying health conditions that, in the trial doctor's judgment, could make the study treatment unsafe or make it difficult to monitor side effects

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
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

Phone: 18622221069

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
Tianjin Medical University Cancer Institute and Hospital
Registry
ClinicalTrials.gov
Start date
1 December 2021
Est. completion
31 December 2023

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Event Free Survival (EFS)

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