Phase 2 Oesophageal Cancer Trial, Recruiting NCT07481058 Sponsor: Beijing Konruns Pharmaceutical Co., Ltd. Condition: Oesophageal Cancer
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Phase 2 Oesophageal Cancer Trial, Recruiting

NCT07481058
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 75 years, of any sex
  • People whose cancer of the esophagus (food pipe) or the junction between the esophagus and stomach has been confirmed by a laboratory test of tissue or cell samples, and is specifically the squamous cell type
  • People who have not yet received any systemic (whole-body) anti-cancer treatment for their current recurrent or metastatic (spread) disease
  • People who have at least one tumor that can be measured on a scan, according to standard criteria called RECIST 1.1
  • People with a general health and activity level rated as 0 or 1 on a standard medical scale (meaning fully active or able to carry out light work)
  • People expected to live longer than 12 weeks
  • People with a Body Mass Index (BMI) of 16.0 or above
  • People whose blood test results show their bone marrow, kidneys, and liver are functioning adequately
  • Women who could become pregnant must have had a negative blood pregnancy test within 7 days before the first treatment dose
  • People who are willing to take part voluntarily and sign a consent form

Who may not be able to join:

  • People who have central nervous system (brain or spinal cord) metastases that are causing symptoms, have not been treated, or are actively getting worse
  • People who have had another type of cancer in the past 5 years
  • People with a known allergic reaction to any monoclonal antibody medicines or chemotherapy ingredients used in the trial
  • People with certain abnormalities affecting the digestive tract (confirm with trial site)
  • People at high risk of bleeding or of developing an abnormal opening (fistula) between the esophagus and nearby organs, or who already have an esophageal or tracheal fistula
  • People with certain heart or blood vessel conditions (confirm with trial site for specific details)
  • People who have previously been treated with anti-angiogenic drugs (medicines that block blood vessel growth to tumors) or immunotherapy
  • People who have received any systemic cancer treatment, experimental drugs, or live vaccines within 4 weeks before the first dose; palliative radiotherapy within 2 weeks before enrollment; or major surgery within 28 days before enrollment
  • People with uncontrolled fluid build-up around the lungs, heart, or abdomen that requires repeated draining
  • People who still have unresolved side effects from previous cancer treatment that have not returned to a mild or absent level
  • People with an active autoimmune disease, or a history of autoimmune disease that required systemic (whole-body) treatment
  • People with active infections, including a serious infection within the past 4 weeks, active tuberculosis, or a positive test for HIV, hepatitis B, or hepatitis C
  • Women who are pregnant or breastfeeding
  • Women who could become pregnant, or men who could father a child, who do not agree to use contraception during the trial and for 6 months after it ends
  • People who have other conditions that the trial doctor judges would increase safety risks or affect the reliability of the trial results

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: +86-010-87788293

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
Beijing Konruns Pharmaceutical Co., Ltd.
Registry
ClinicalTrials.gov
Start date
12 December 2025
Est. completion
1 December 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Objective Response Rate (ORR)

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