Phase 2 Oesophageal Cancer Trial, Recruiting
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, have signed a consent form, and are able to attend follow-up appointments
- You have been diagnosed with esophageal cancer confirmed by a tissue biopsy, at a specific stage that has not spread to distant parts of the body (confirm with trial site for exact staging details)
- You are between 18 and 75 years old (male or female)
- You are generally able to carry out daily activities with little to no limitation (your doctor can assess this)
- You have at least one tumor that can be measured or assessed on scans
- You have not received any previous treatment for esophageal cancer, such as radiotherapy, chemotherapy, or surgery
- Your lung function is at an acceptable level to safely undergo esophageal cancer surgery (confirm with trial site)
- You have no medical reasons that would prevent you from having surgery
- Your blood counts, kidney, liver, and blood clotting results are within acceptable ranges as measured by recent blood tests (confirm with trial site for specific values)
- If you could become pregnant, you must use an approved form of contraception during the study and for 6 months after treatment ends, have a negative pregnancy test within 72 hours before joining, and must not be breastfeeding
Who may not be able to join:
- Your cancer has spread to other parts of the body (stage IV) or cannot be removed by surgery
- Your cancer is located in the upper (neck) section of the esophagus
- You have a known allergy to any of the study drugs, including the immunotherapy drug (camrelizumab), albumin-bound paclitaxel, carboplatin, or similar platinum-based drugs
- You have moderate or severe chest or back pain, or there is a risk that your esophagus could develop a hole (perforation)
- You have previously received radiotherapy, chemotherapy, or any other cancer treatment for this cancer
- You have taken strong immune-suppressing medications within the past 2 weeks (with some exceptions — confirm with trial site)
- You received a live vaccine within 4 weeks before starting the study
- You had major surgery or a serious injury within 4 weeks before starting the study
- You have an active autoimmune disease or a history of certain autoimmune conditions (some exceptions may apply — confirm with trial site)
- You have a history of immune system problems, HIV, or have had an organ or bone marrow transplant
- You have significant uncontrolled heart problems, such as heart failure, unstable chest pain, a heart attack within the past year, or serious uncontrolled irregular heartbeat
- You had a serious infection requiring hospital treatment within the past 4 weeks, or have signs of an active infection shortly before joining the study
- You have active tuberculosis (TB) or a history of TB that was not properly treated
- You have active hepatitis B or hepatitis C infections at certain levels (confirm with trial site)
- You have been diagnosed with another cancer within the past 5 years, with some exceptions for certain low-risk skin cancers or early cervical conditions
- You are pregnant or breastfeeding
- In the opinion of the study doctor, other serious medical, psychiatric, or personal circumstances that could affect your safety or ability to take part in 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.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Event-free survival (EFS)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.