Oesophageal Cancer Trial, Recruiting NCT05392413 Sponsor: Nanfang Hospital, Southern Medical University Condition: Oesophageal Cancer
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Oesophageal Cancer Trial, Recruiting

NCT05392413
Recruiting Not Applicable

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 stage IV squamous cell carcinoma of the oesophagus (a specific type of advanced oesophageal cancer), confirmed by a tissue or cell sample, and who are planned to receive a combination of a PD-1 immunotherapy drug and a TP chemotherapy regimen.
  • People whose general physical functioning falls within a certain range on a standard medical scale (rated 0–2 on the ECOG scale, meaning able to carry out at least some daily activities — confirm with trial site).
  • People who have at least one tumour that can be measured on scans.
  • People whose life expectancy is expected to be more than 3 months.
  • People who have had previous cancer treatment where any side effects from that treatment have returned to their normal baseline levels, or are at a mild level (grade 1 or below), before joining the trial (except for ongoing hair loss from prior treatment).
  • People of reproductive age who agree to use effective contraception from the time of signing the consent form until 6 months after the last dose of the study drug — this applies to both male and female participants and their partners.
  • People whose blood test results meet specific health thresholds, including healthy enough levels of white blood cells, platelets, haemoglobin, liver function markers, and kidney function (confirm specific values with trial site).

Who may not be able to join:

  • People who currently have, or have a history of, an autoimmune disease that is likely to come back (such as lupus, rheumatoid arthritis, inflammatory bowel disease, autoimmune thyroid disease, vasculitis, or psoriasis), or people who are considered at risk of immune-related complications (for example, organ transplant recipients who require immune-suppressing medication).
  • People who have needed to take steroid medications (such as prednisone above a certain dose) or other immune-suppressing drugs within the 14 days before starting the study treatment.
  • People who have had major surgery, high-dose radiation therapy, or palliative radiation therapy within the 14 days before starting study treatment, or certain radioactive treatments within the 56 days before starting.
  • People who have received any systemic cancer treatment — including immunotherapy or certain biological therapies — within the 14 days before starting study treatment.
  • People who have had certain lung conditions, such as interstitial lung disease, inflammation of the lungs, pulmonary fibrosis, or acute lung disease (with some exceptions — confirm with trial site), or who have uncontrolled diabetes or uncontrolled high blood pressure.
  • People living with HIV.
  • People who currently have active tuberculosis.
  • People who have had an active infection requiring intravenous (IV) antibiotic or antiviral treatment within the 2 weeks before the first dose.
  • People who have previously received a solid organ transplant.
  • People who have previously received any immunotherapy drug that targets immune checkpoint proteins, such as anti-PD-1 or anti-PD-L1 treatments.

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 28 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Lei Zheng, Nanfang Hospital, Southern Medical University

Phone: 18665000310

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
Not Applicable
Sponsor
Nanfang Hospital, Southern Medical University
Registry
ClinicalTrials.gov
Start date
1 August 2022
Est. completion
31 December 2025

Where this trial is recruiting

🇨🇳 China

Primary endpoints

peripheral blood immune cells and immune molecules; Imaging examination

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: 28 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