Phase 2 Oesophageal Cancer Trial, Recruiting NCT07339488 Sponsor: Chuangzhen Chen Condition: Oesophageal Cancer
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Phase 2 Oesophageal Cancer Trial, Recruiting

NCT07339488
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 are willing to take part voluntarily, agree to follow the study requirements, and sign a consent form
  • People aged 18 to 75 years (any sex)
  • People whose general health and ability to carry out daily activities falls within a certain range, as measured by a standard medical scale (ECOG score of 0–1; confirm with trial site)
  • People who have been confirmed through laboratory testing of tissue samples to have a specific type of esophageal cancer called squamous cell carcinoma, before any surgery
  • People whose cancer is located in the chest portion of the oesophagus (food pipe)
  • People whose cancer cannot be fully removed by surgery — this includes cancer that has grown into nearby structures, cancer with certain lymph node involvement, or cases where the surgeon has determined surgery is not feasible (confirm with trial site for full details)
  • People who have never previously received any cancer treatment, including chemotherapy, hormone therapy, radiation therapy, or immunotherapy
  • People whose recent blood test results (taken within 7 days before joining) show that blood counts, liver function, kidney function, blood clotting, thyroid function, and heart pumping strength all fall within the required ranges (confirm specific values with trial site)
  • Women who agree to use contraception during the study and for 6 months afterward, have a negative pregnancy test within 7 days before joining, and are not breastfeeding; and men who agree to use contraception during the study and for 6 months afterward
  • People who have no psychological, family, social, or location-related factors that could make it difficult to follow the study plan

Who may not be able to join:

  • People whose cancer has spread to distant parts of the body, other than to lymph nodes near the collarbone
  • People who have, or are at high risk of, a tear or hole in the oesophagus
  • People for whom radiation therapy or certain immunotherapy drugs (called immune checkpoint inhibitors) are medically unsuitable
  • People who previously had serious side effects from immunotherapy drugs
  • People who received radiation therapy to the chest, abdomen, or pelvis within the 6 months before joining
  • People who still have side effects from previous cancer treatment that have not sufficiently settled down (unless the trial doctors consider those effects to pose no safety risk)
  • People with active infections (bacterial, viral, or fungal) that are not well controlled despite treatment
  • People with breathing difficulties, airway blockage, or low oxygen in the body's tissues
  • People with significant heart disease (classified as NYHA Class II or higher; confirm with trial site)
  • People with markedly abnormal liver or kidney function (certain test results more than 3 times the upper limit of normal)
  • People with active hepatitis B, hepatitis C, HIV, or syphilis
  • People with active brain disease, cancer that has spread to the brain or surrounding membranes with significant symptoms, or difficulties with decision-making
  • People with known allergies to any of the drugs used in this trial
  • People with current drug or alcohol misuse
  • Women who are pregnant or breastfeeding
  • People who are currently taking part in another treatment-based clinical trial
  • People who had a major surgical procedure within 30 days before joining
  • People who used antibiotics, antifungal, antiviral, or antiparasitic medications within 4 weeks before joining

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 16 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: +86 13923995569

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
Sponsor
Chuangzhen Chen
Registry
ClinicalTrials.gov
Start date
5 December 2025
Est. completion
1 November 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Pathological Complete Response (pCR) 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: 16 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