Phase 2 Oesophageal Cancer Trial, Recruiting NCT07071103 Sponsor: Chuangzhen Chen Condition: Oesophageal Cancer
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Phase 2 Oesophageal Cancer Trial, Recruiting

NCT07071103
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 aged 18 to 80 years, of any gender
  • People who are reasonably active and able to care for themselves, or who need only limited help with daily activities (this is measured using a standard scale called ECOG, levels 0–2)
  • People with a life expectancy of more than 3 months
  • People who have at least one measurable tumour site that can be tracked over time using standard imaging measurements
  • People with solid tumours that have spread to other parts of the body (of any tumour type), where no standard treatment options remain, and whose cancer got worse after previously receiving immunotherapy, immunotherapy combined with chemotherapy, or immunotherapy combined with anti-blood-vessel-targeting treatment
  • People who are not considered suitable candidates for surgery
  • People who have brain metastases (cancer that has spread to the brain) that have been assessed as stable following treatment, confirmed by repeated CT and/or MRI scans
  • People who have complete medical and pathology records available
  • People who are not facing personal, family, social, or location-related circumstances that would make it difficult to follow the trial requirements
  • People who are able to understand and voluntarily sign an informed consent form

Who may not be able to join:

  • People for whom radiation therapy or immunotherapy is medically not suitable
  • People who have previously experienced serious immune-related side effects that were not tolerable, such as immune-related heart inflammation or lung inflammation
  • People whose cancer was assessed as having rapidly progressed (grown faster than expected) during prior immunotherapy — sometimes called hyperprogressive disease
  • People who have received radiation therapy to the pelvis or abdomen within the 6 months before joining the trial
  • People whose side effects from previous treatments have not yet recovered to a mild level (based on a standard grading scale), except for side effects already confirmed to be low-risk, such as tiredness or hair loss
  • People with active infections (bacterial, viral, or fungal) that are not controlled despite treatment
  • People with significant liver or kidney problems, shown by blood test results more than 3 times above the normal upper limit
  • People with active hepatitis B, hepatitis C, HIV, or syphilis
  • People with brain disorders, active symptoms from cancer spread to the brain or surrounding membranes, or significant problems with thinking or memory
  • People who have a known allergy or sensitivity to any of the drugs used in this trial
  • People with a current problem with drug and/or alcohol misuse
  • People who are pregnant or breastfeeding
  • People who are currently taking part in another treatment-based clinical trial
  • People with poorly controlled fluid build-up around the lungs, heart, or abdomen that requires drainage more than once every 14 days
  • People who have had major surgery within the 30 days before joining the trial
  • People who have taken antibiotics, antifungal, antiviral, antiparasitic medications, or probiotics within the 4 weeks before joining the trial

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 14 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
26 September 2025
Est. completion
1 January 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Objective Response Rate (ORR); Disease Control Rate(DCR); Progression Free Survival while Receiving ILDR combined Therapy (PFS2); Incidence of Abscopal Effect

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: 14 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