Phase 2 Oesophageal Cancer Trial, Recruiting NCT06637163 Sponsor: Shanghai Zhongshan Hospital Condition: Oesophageal Cancer
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Phase 2 Oesophageal Cancer Trial, Recruiting

NCT06637163
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 and agree to follow the study requirements by signing a consent form.
  • People aged 18 or older, of any gender.
  • People who are generally well enough to carry out daily activities with little or no limitation (based on a standard health performance scale scored 0 or 1).
  • People who have been confirmed by tissue testing to have a specific type of esophageal cancer (squamous cell carcinoma) that has not spread to distant parts of the body, and whose cancer is considered removable by surgery, at certain defined stages.
  • People who have not previously received any treatment for esophageal cancer, including chemotherapy, hormone therapy, radiation, or immunotherapy.
  • People whose recent blood test results (taken within 7 days before joining) show that blood cell counts, liver function, kidney function, blood clotting, thyroid hormone levels, and heart pumping function all fall within the ranges required by the trial.
  • Women who agree to use effective contraception during the study and for 6 months after it ends, have a negative pregnancy test within 7 days before joining, and are not breastfeeding.
  • Men who agree to use effective contraception during the study and for 6 months after it ends.
  • People who carry certain markers for hepatitis B (HBsAg or HBcAb positive) may still be considered if their hepatitis B virus levels are low enough and they are receiving or will begin appropriate antiviral treatment (confirm with trial site).

Who may not be able to join:

  • People who have another type of cancer, except for a previously cured form of skin cancer called basal cell carcinoma.
  • People whose esophageal cancer is located in the cervical (neck) portion of the esophagus.
  • People who have had a severe allergic reaction to another monoclonal antibody treatment in the past.
  • People who have an active autoimmune disease or a history of one — such as autoimmune liver disease, lung inflammation, bowel inflammation, blood vessel inflammation, kidney inflammation, or asthma needing certain medications — though some milder conditions may be acceptable (confirm with trial site).
  • People who are currently taking immunosuppressant medications or steroid medications at doses above a certain level, and have continued taking them within 2 weeks before the first study dose.
  • People who have fluid build-up around the lungs, heart, or abdomen that is uncontrolled and requires repeated draining.
  • People who have uncontrolled symptoms from cancer that has spread to the brain or spine, or evidence of such spread found on a scan, within 4 weeks before the first study dose.
  • People with serious uncontrolled heart conditions, such as a recent or ongoing lack of blood flow to the heart, a heart attack, a significant irregular heartbeat, moderate to severe heart failure, or reduced heart pumping function below a certain level.
  • People with a serious active or uncontrolled infection of a certain severity.
  • People who have received a live or preventive vaccine within 4 weeks before the first study dose.
  • People who have other serious illnesses — including mental health conditions — significant abnormal test results, or personal or social circumstances that the study doctor believes could make participation unsafe or lead to early withdrawal.
  • People who test positive for hepatitis C virus and have virus levels above a certain amount in their blood.
  • People who test positive for HIV.

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 15 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: Lijie Tan, Professor, Fudan University

Phone: +8613681972151

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
24 October 2024
Est. completion
1 April 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Pathological complete response (pCR)

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: 15 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