Phase 4 Colorectal Cancer Trial, Recruiting NCT06118762 Sponsor: The First Affiliated Hospital of Nanchang University Condition: Colorectal Cancer
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Phase 4 Colorectal Cancer Trial, Recruiting

NCT06118762
Recruiting Phase 4

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 fully understood the study and have signed a consent form agreeing to take part
  • People aged 18 or older, of any gender
  • People who have been diagnosed with advanced or metastatic colorectal cancer (a type of bowel cancer that has spread), confirmed by a tissue sample test
  • People whose cancer got worse during, or who could not tolerate, at least one prior standard treatment containing the chemotherapy drugs fluorouracil, oxaliplatin, and irinotecan
  • People who have at least one tumour that can be measured on a scan, according to standard measurement guidelines
  • People who have a good general level of physical functioning, rated 0 or 1 on a standard medical scale (meaning fully active or able to carry out light activities)
  • People with an expected survival of at least 12 weeks
  • People whose blood counts and organ function results meet specific minimum levels in the 14 days before joining (covering blood cell counts, liver function, kidney function, and related measures — confirm details with the trial site)
  • People who are willing and able to use effective contraception, if they are a woman of childbearing age or a man whose partner wishes to become pregnant

Who may not be able to join:

  • People who have previously been treated with Fruquintinib, or similar drugs that target blood vessel growth (such as Apatinib, Regorafenib, or Anlotinib)
  • People who have previously been treated with the chemotherapy drug Raltitrexed
  • People who have taken part in another drug clinical trial and received at least one dose within the four weeks before joining, or who have received any other cancer treatment (such as chemotherapy, immunotherapy, or hormone therapy) within the four weeks before joining
  • People who have a condition that affects how the body absorbs medication, or who are unable to swallow Fruquintinib tablets
  • People who currently have certain stomach or bowel conditions, such as active ulcers, ulcerative colitis, active bleeding from a tumour, or other conditions that may raise the risk of bleeding or a hole forming in the gut
  • People who have active bleeding or a tendency to bleed
  • People with a serious history of heart or brain blood vessel disease, including stroke (with some exceptions), heart attack, unstable chest pain, or poorly controlled heart rhythm problems within the six months before joining — or people with poor heart function based on standard medical ratings
  • People who have had another type of cancer within the past five years (with the exception of certain fully treated skin cancers or cervical pre-cancer)
  • People with clinically uncontrolled active infections, such as active pneumonia, or active hepatitis B or C at levels above specified limits
  • People with brain metastases that are causing symptoms, or people with cancer that has spread to the lining around the brain (cancerous meningitis) — people with previously treated, stable brain metastases may be considered if specific conditions are met (confirm with the trial site)
  • People who are pregnant or breastfeeding
  • People with high blood pressure that cannot be controlled with medication, defined as blood pressure remaining at or above 140/90 mmHg while taking blood pressure medication
  • People whose urine or 24-hour urine protein tests show levels above specified limits
  • People considered unsuitable for the trial by the investigating doctors, 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 12 July 2026
Phase 4 trials study a drug that has already been approved, monitoring long-term safety and effectiveness in real-world use.

Contact this trial

Principal Investigator: Xiaodong Peng, Director, The First Affiliated Hospital of Nanchang University

Phone: 0086-457-079186427246

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 4
Sponsor
The First Affiliated Hospital of Nanchang University
Registry
ClinicalTrials.gov
Start date
20 October 2023
Est. completion
1 October 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Progression free survival (PFS)

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: 12 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