Colorectal Cancer Trial, Recruiting NCT06751953 Sponsor: The First Affiliated Hospital of Nanchang University Condition: Colorectal Cancer
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Colorectal Cancer Trial, Recruiting

NCT06751953
Recruiting Not Applicable

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 who have been diagnosed with colorectal cancer (bowel cancer) confirmed by a tissue or cell test
  • People who have at least one tumour that can be measured on a scan
  • People aged between 18 and 70 years old, of any gender
  • People whose cancer has continued to grow or spread after receiving two standard lines of treatment, and who have finished their last cancer treatment at least 2 weeks before joining
  • People who are expected to live for at least 3 months
  • People who are relatively well and able to carry out daily activities with little or no limitation (as assessed by a standard medical scale called ECOG 0–1)
  • Women of childbearing age who have a negative pregnancy test and are willing to use effective contraception, with no plans to become pregnant within six months of being in the study
  • People who are able to complete all the required blood and laboratory tests during the screening period
  • People whose heart, liver, and kidney are functioning normally
  • People whose blood test results fall within acceptable ranges, including healthy levels of white blood cells, red blood cells, platelets, and normal liver and kidney function markers (confirm specific values with trial site)
  • People who do not have active hepatitis, HIV/AIDS, syphilis, or other active infectious diseases
  • People whose inflammation markers (such as CRP, ASO, and erythrocyte sedimentation rate) fall within acceptable ranges (confirm specific values with trial site)
  • People whose thyroid hormone levels are within the normal ranges required by the trial (confirm specific values with trial site)
  • People whose adrenal hormone (ACTH) levels fall within the required range (confirm specific values with trial site)
  • People who are able to understand the study and are willing to sign a consent form of their own free will

Who may not be able to join:

  • People who have brain metastases (cancer that has spread to the brain) that cannot be controlled
  • People who are expected to need any other cancer treatment during the study, including chemotherapy, maintenance drug therapy, or surgery
  • People who have needed high-dose steroid tablets or other immune-suppressing medicines within the 14 days before starting the trial (inhaled or skin-applied steroids may be acceptable in some cases — confirm with trial site)
  • People who have received certain immunotherapy or immune-stimulating cancer treatments within the 3 months before starting the trial
  • People who are currently taking part in another clinical trial, or who finished a previous clinical trial less than 4 weeks (or 5 half-lives of that study drug) before starting this one
  • People who have had serious heart or blood vessel problems — such as a heart attack, stroke, or unstable heart rhythm — within the past 1 to 3 months before starting the trial
  • People with uncontrolled reduced blood supply to the heart or uncontrolled irregular heart rhythms
  • People with high blood pressure that remains uncontrolled despite medication (systolic above 150 mmHg or diastolic above 100 mmHg)
  • People who have had significant or unexplained bleeding within the 3 months before joining, or whose tumour is considered likely to involve or invade a major blood vessel, or who have coughed up a meaningful amount of blood in the month before starting
  • People who have had a blood clot event — such as a stroke, mini-stroke, deep vein thrombosis, or pulmonary embolism — within the 3 months before screening
  • People with active tuberculosis
  • People who have had a serious infection (such as one requiring hospitalisation or severe pneumonia) within the 4 weeks before starting, or who have any currently active infection
  • People who are planning to have, or who have previously had, an organ or tissue transplant
  • People with uncontrolled epilepsy, brain or nervous system disorders that affect thinking or cognition
  • People who have had their spleen removed
  • Women who are pregnant or breastfeeding
  • People with a history of severe allergies or a strong tendency toward allergic reactions
  • People who have had a problem with ongoing alcohol or drug misuse in the 6 months before enrolling
  • People who the trial doctor considers unsuitable for the study for any other reason

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
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Phone: 15879155066

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

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Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
The First Affiliated Hospital of Nanchang University
Registry
ClinicalTrials.gov
Start date
1 September 2024
Est. completion
31 August 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Objective response rate (ORR); Disease control rate (DCR); Drug safety

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