Phase 3 Oesophageal Cancer Trial, Recruiting NCT06190782 Sponsor: Fudan University Condition: Oesophageal Cancer
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Phase 3 Oesophageal Cancer Trial, Recruiting

NCT06190782
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 aged 18 or older
  • People who are relatively well and able to carry out daily activities with little or no limitation (as measured by a standard health scale called ECOG, scored 0 or 1)
  • People diagnosed with a specific type of oesophageal (food pipe) cancer called squamous cell carcinoma
  • People whose cancer has spread to a limited number of sites, specifically no more than 4 distant spread sites in total, no more than 3 spread sites within any single organ, and where each spread site measures no larger than 5cm across
  • People who have at least 1 spread site that has been confirmed by a tissue sample (biopsy or similar test)

Who may not be able to join:

  • People whose cancer has previously spread widely throughout the body, or whose limited spread is considered to be a result of treatment reducing previously widespread disease (confirm with trial site)
  • People who have a hole in or active bleeding from the oesophagus (food pipe)
  • People whose cancer continued to grow or spread while being treated with a type of immunotherapy drug called a PD-1 inhibitor
  • People whose cancer has come back in an area that was previously treated with radiation therapy
  • People who are unable to tolerate chemotherapy or immunotherapy treatments
  • People whose lungs have received a level of radiation exposure above a specific safety threshold during prior treatment (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 16 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: Kuaile Zhao, MD, Fudan University

Phone: 86-18017317882

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
Registry
ClinicalTrials.gov
Start date
27 September 2022
Est. completion
27 September 2025

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Progression-free survival difference of PD-1 inhibitor+radiotherapy and PD-1 inhibitor alone

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