Phase 2 Colorectal Cancer Trial, Recruiting NCT06980532 Sponsor: Liu Huang Condition: Colorectal Cancer
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Phase 2 Colorectal Cancer Trial, Recruiting

NCT06980532
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 who have been fully informed about the study and have agreed to take part by signing a consent form
  • Adults aged 18 or older
  • People who have been diagnosed with colorectal cancer that has spread and cannot be removed by surgery, and whose tumour has been confirmed to be microsatellite stable (MSS) — a specific characteristic of the tumour's genetic makeup
  • People whose tumour shows a specific change in a gene called MET — either an amplification (too many copies of the gene) or overexpression (the MET protein is present at high levels) — confirmed through specific laboratory tests
  • People whose cancer has continued to grow or spread after receiving two previous courses of standard cancer treatment, confirmed by imaging scans
  • People who have at least one tumour that can be measured on imaging scans, according to standard criteria (RECIST 1.1)
  • People with a good general level of physical functioning, rated 0 or 1 on a standard scale used in cancer trials (meaning fully active or able to carry out light activity)
  • People whose life expectancy is estimated to be at least 3 months
  • People whose blood counts meet minimum levels — including neutrophils, platelets, haemoglobin, and white blood cells — without the need for recent blood transfusions or growth factor medications
  • People whose liver and kidney function test results fall within acceptable ranges as defined by the trial
  • People whose blood clotting test results fall within acceptable ranges
  • Women who could become pregnant must have a negative pregnancy test within 7 days before joining, must not be breastfeeding, and must be willing to use contraception during the trial and for 6 months after the last dose; male participants must also agree to use contraception during the trial and for 6 months after it ends

Who may not be able to join:

  • People who have previously been treated with a MET inhibitor (a type of targeted cancer drug)
  • People whose colorectal cancer has a different genetic profile called MSI-H or dMMR (a sign that the tumour has certain DNA repair problems)
  • People whose tumour has a BRAF gene mutation and who have not yet received treatment with BRAF or MEK inhibitors
  • People with serious active bleeding, active peptic ulcers, unhealed holes in the digestive tract, or fistulas (abnormal connections in the digestive tract)
  • People who have had a severe allergic reaction to any of the study drugs or their ingredients
  • People with serious uncontrolled infections or other serious uncontrolled medical conditions, or moderate to severe kidney problems (such as uncontrolled high blood pressure, uncontrolled diabetes, or ongoing serious infections)
  • People with active hepatitis B or C infection, based on specific blood test thresholds
  • People who are HIV positive
  • People who have had or currently have another type of cancer, with some exceptions — such as certain well-controlled skin cancers, early-stage breast or cervical cancer, or other cancers that have been well-controlled without treatment for the past five years
  • Women who are pregnant or breastfeeding, or people of childbearing potential who are unwilling to use contraception
  • People who currently need treatment for another cancer
  • People whom the trial investigators consider unsuitable for the study for other reasons

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 22 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: 13667241722

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
Liu Huang
Registry
ClinicalTrials.gov
Start date
25 April 2025
Est. completion
30 December 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Recommended dose for Phase II; 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: 22 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