Phase 2 Oesophageal Cancer Trial, Recruiting NCT06446726 Sponsor: Sichuan University Condition: Oesophageal Cancer
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Phase 2 Oesophageal Cancer Trial, Recruiting

NCT06446726
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:

  • You have been diagnosed with a specific type of esophageal cancer (squamous cell carcinoma) located in the chest area, confirmed by a tissue biopsy, at a stage that has not spread to distant parts of the body
  • Your doctors believe surgery could completely remove the cancer (with clear margins)
  • You are generally able to carry out daily activities with little to no restriction (feeling well or only mildly limited)
  • You are between 18 and 75 years old
  • Your blood counts are healthy enough without needing transfusions or extra medications: enough white blood cells, infection-fighting cells, platelets, and red blood cells
  • A specialist has confirmed your lungs and heart are working well enough, with no severe breathing problems or acute heart failure
  • Your liver is functioning well, based on blood test results within acceptable ranges
  • Your kidneys are functioning well, based on blood test results within acceptable ranges
  • You are willing to take part voluntarily, sign a consent form, and attend all required visits and follow all study procedures
  • Your doctors expect you to live longer than 6 months
  • You agree to have surgery, radiation therapy, chemotherapy, and immunotherapy as part of the trial
  • If you could become pregnant, you have had a negative pregnancy test within 7 days before starting treatment; all participants agree to use effective contraception during the trial and for 8 weeks after the last dose
  • You do not have a hole (perforation) or active bleeding in your esophagus, and the cancer has not grown into your windpipe or major chest blood vessels
  • You have at least one area of cancer that can be measured on a scan

Who may not be able to join:

  • You are not suitable for the specific immunotherapy or chemotherapy drugs used in this trial (confirm with trial site)
  • You have previously received any treatment for this esophageal cancer, including chemotherapy, radiotherapy, experimental drugs, or certain immune checkpoint therapies (such as anti-PD-1 or anti-PD-L1 drugs)
  • Your cancer has previously caused an abnormal passage (fistula) to form
  • Your doctors believe you are at high risk of developing a fistula or signs of a hole forming in the esophagus
  • You have needed high-dose steroid tablets or other immune-suppressing medicines in the 14 days before starting the trial (some low-dose or short-term steroid use may still be acceptable — confirm with trial site)
  • You have an active autoimmune disease (where your immune system attacks your own body), or a history of one that could come back — though some well-controlled conditions like type 1 diabetes, an underactive thyroid, or certain skin conditions may still be eligible (confirm with trial site)
  • You have a history of scarring lung disease, non-infectious lung inflammation, or poorly controlled lung conditions such as pulmonary fibrosis
  • You currently need antibiotics, antifungal, or antiviral treatment for an active infection such as tuberculosis, or you have had a serious infection requiring hospitalisation in the past 4 weeks, or have taken antibiotic tablets or drips in the past 2 weeks
  • You have previously had an organ transplant (other than a cornea transplant) or a bone marrow/stem cell transplant from another person
  • You are known to be allergic to the study drug (tiragolumab) or to any of the chemotherapy drugs used in this trial
  • You have significant heart problems such as serious irregular heartbeat, heart block, unstable chest pain, or heart failure affecting your daily life

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 19 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: Jianxin Xue, professor, West China Hospital

Phone: +86 18980606739

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
Sichuan University
Registry
ClinicalTrials.gov
Start date
30 June 2024
Est. completion
30 June 2025

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Pathologic complete response

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: 19 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