Phase 2 Oesophageal Cancer Trial, Recruiting NCT07437898 Sponsor: The Affiliated Hospital of Putian University Condition: Oesophageal Cancer
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Phase 2 Oesophageal Cancer Trial, Recruiting

NCT07437898
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 are willing to take part and have signed a consent form agreeing to join the study
  • You are between 18 and 75 years old (male or female)
  • You have been diagnosed with a specific type of esophageal (food pipe) cancer called squamous cell carcinoma, confirmed by a tissue or cell sample
  • Your cancer is at a certain stage — it has not spread to distant parts of the body, but may have spread to nearby lymph nodes or grown into surrounding tissue (confirm with trial site for exact staging)
  • You have at least one area of cancer that can be measured on a scan, meeting specific size requirements
  • Doctors believe your cancer can be fully removed by surgery (known as an R0 resection)
  • You are generally able to carry out daily activities with little or no limitation (confirm with trial site)
  • You have not had any previous treatment for your esophageal cancer, including surgery, radiotherapy, or chemotherapy
  • You are planning to have surgery after completing the pre-surgery treatment in this trial
  • You have no medical reasons preventing you from having surgery
  • Your blood counts, liver function, kidney function, and blood clotting results are within acceptable ranges as confirmed by recent blood tests
  • If you are a woman who could become pregnant, you have a negative pregnancy test within 72 hours before starting the trial and agree to use effective contraception during the trial and for at least 3 months after your last dose
  • If you are a man whose partner could become pregnant, you agree to use effective contraception during the trial and for at least 3 months after your last dose
  • You are willing and able to follow the study schedule and attend all required follow-up appointments

Who may not be able to join:

  • Your cancer has grown significantly into nearby important structures such as major blood vessels or the windpipe
  • You have fluid build-up around your lungs, heart, or abdomen that is uncontrolled and requires repeated draining
  • You are underweight with a Body Mass Index (BMI) below 18.5 — though you may still be considered if your weight improves with nutritional support before joining (confirm with trial site)
  • You have had a serious allergic reaction to monoclonal antibody medicines, or to any of the specific drugs used in this trial (adebrelimab, paclitaxel, cisplatin, or similar platinum-based medicines)
  • You have previously had any cancer treatment, including radiotherapy, chemotherapy, immunotherapy, or targeted therapy
  • You have taken strong immune-suppressing steroid medicines (above a certain dose) within the past 2 weeks — some lower-dose or topical steroids may be allowed (confirm with trial site)
  • You have received a live vaccine within the past 4 weeks before starting the trial
  • You have had major surgery or a serious injury within the past 4 weeks before starting the trial
  • You have an active autoimmune disease (where your immune system attacks your own body), or a history of certain autoimmune conditions — some exceptions may apply, such as thyroid conditions well-controlled with medication or fully resolved skin or childhood allergy conditions (confirm with trial site)
  • You have a weakened immune system, including a positive HIV test, any inherited or acquired immune disorder, or a history of organ or bone marrow transplant
  • You have significant heart problems, including moderate-to-severe heart failure, unstable chest pain, a heart attack within the past year, or poorly controlled irregular heart rhythms
  • You have had a serious infection within the past 4 weeks, or have signs of active infection or have needed antibiotic treatment (other than preventive antibiotics) within the past 2 weeks
  • You have active tuberculosis (TB), had active TB within the past year, or had TB more than a year ago that was not properly treated
  • You have a hereditary bleeding disorder or blood clotting problem, or have had significant bleeding episodes (such as gastrointestinal bleeding) within the past 3 months
  • You have been diagnosed with another cancer within the past 5 years — some low-risk skin cancers or cervical pre-cancers that have been fully treated may be exceptions (confirm with trial site)
  • You are currently pregnant or breastfeeding
  • You have other serious medical or personal circumstances that the study doctor believes could make it unsafe for you to participate or prevent you from completing the study

**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 2 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.

GP referral letter

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Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
The Affiliated Hospital of Putian University
Registry
ClinicalTrials.gov
Start date
3 September 2024
Est. completion
1 April 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Pathological Complete Response Rate (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: 2 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