Phase 3 Oesophageal Cancer Trial, Recruiting NCT06194734 Sponsor: Beijing Konruns Pharmaceutical Co., Ltd. Condition: Oesophageal Cancer
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Phase 3 Oesophageal Cancer Trial, Recruiting

NCT06194734
Recruiting Phase 3

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, male or female
  • People whose cancer has been confirmed by laboratory testing (biopsy or cell sample) to be squamous cell carcinoma of the esophagus or the junction between the esophagus and stomach
  • People whose esophageal squamous cell carcinoma has come back or spread, and who have already received treatment with a PD-1 or PD-L1 immunotherapy drug, plus at least two prior lines of treatment overall
  • People who have at least one tumor that can be measured on scans, according to standard criteria (called RECIST 1.1)
  • People with a good general health and activity level, rated 0 or 1 on a standard scale used by doctors (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 at least 16.0 and a body weight of at least 40 kg
  • People whose blood test results show their bone marrow, kidneys, and liver are functioning well enough
  • Women who could become pregnant must have a negative blood pregnancy test done within 7 days before joining the trial
  • People who are willing to take part voluntarily and sign a consent form

Who may not be able to join:

  • People with cancer that has spread to the brain or spinal cord (central nervous system) that has not been treated
  • People who have had another type of cancer within the past 5 years
  • People with certain abnormalities or problems affecting the digestive system (confirm with trial site for specifics)
  • People with certain heart or blood vessel conditions (confirm with trial site for specifics)
  • People who have previously received a type of drug that targets blood vessel growth (vascular targeting inhibitor)
  • People who have previously been treated with any of these specific medicines: Irinotecan, Docetaxel, or Tegafur Gimeracil Oteracil Potassium
  • People who have taken part in another clinical trial within the 4 weeks before joining; or who have had radiotherapy, immunotherapy, or surgery for cancer within the 4 weeks before joining; or who have taken certain targeted cancer drugs within 2 weeks or 5 half-lives (whichever is longer); or who have had chemotherapy within 3 weeks or 5 half-lives (whichever is longer)
  • People who still have unresolved side effects from previous cancer treatment that have not returned to a mild or absent level
  • People with large amounts of fluid build-up in the abdomen, around the lungs, or around the heart that cannot be controlled
  • People who have had a serious infection within the 4 weeks before joining
  • People with a known HIV infection, or currently active hepatitis B or C infection
  • Women who are pregnant or breastfeeding
  • Women who could become pregnant, or men who could father a child, who are not willing to use contraception during the trial and for 6 months after it ends
  • People considered ineligible for any other reason, as assessed by the trial doctors

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 23 July 2026
Phase 3: approximately ~65% 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: Jing Huang, Ph.D, Cancer Institute and Hospital, Chinese Academy of Medical Sciences

Phone: 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 3
Sponsor
Beijing Konruns Pharmaceutical Co., Ltd.
Registry
ClinicalTrials.gov
Start date
5 February 2024
Est. completion
30 December 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Overall survival (OS)

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: 23 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