Phase 3 Colorectal Cancer Trial, Recruiting NCT06992648 Sponsor: Second Affiliated Hospital, School of Medicine, Zhejiang University Condition: Colorectal Cancer
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Phase 3 Colorectal Cancer Trial, Recruiting

NCT06992648
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 who have signed a consent form before any study procedures begin
  • Adults aged 18 or older
  • People with a confirmed diagnosis (from a tissue sample) of colon or rectal cancer that cannot be surgically removed, specifically the type called adenocarcinoma
  • People whose tumour has already been tested to determine whether a gene called RAS is mutated or normal
  • People who have previously received certain standard cancer treatments for advanced colorectal cancer, including specific chemotherapy drugs and targeted antibody treatments (the exact combinations required depend on RAS test results — confirm with trial site)
  • People whose cancer can be measured or tracked using standard imaging criteria
  • People who are able to swallow tablets
  • People with an estimated life expectancy of at least 12 weeks
  • People who are reasonably active and able to care for themselves, with only mild limitations on physical activity (confirm with trial site)
  • People whose blood counts, kidney function, liver function, urine protein, and blood clotting levels meet the specific thresholds set by the trial, based on tests done within 7 days before joining
  • Women who could become pregnant must have had a negative blood pregnancy test within 7 days before joining
  • All participants must agree to use a highly effective form of contraception during the study and for at least 6 months after the last dose

Who may not be able to join:

  • People who have previously been treated with a drug called trifluridine/tipiracil, or with a type of targeted drug called a TKI, for advanced colorectal cancer
  • People who are pregnant, breastfeeding, or may become pregnant during the study
  • People who have received any cancer treatment within 4 weeks before joining
  • People who have not recovered from serious side effects (grade 3 or higher) from previous cancer treatments, not including hair loss or skin colour changes
  • People with brain or nervous system spread of their cancer that is causing symptoms and is not stable, or that requires increasing doses of steroid medication to manage
  • People with a severe or uncontrolled active infection
  • People with a current or past history of a lung condition called interstitial lung disease, pneumonitis, or high blood pressure in the lungs
  • People with active significant liver inflammation, including from Hepatitis B or Hepatitis C infection
  • People known to carry HIV antibodies
  • People with high blood pressure that is not controlled (blood pressure of 150/100 or above), or with an uncontrolled or symptomatic heart rhythm problem
  • People who have had a stroke or heart attack within the 6 months before joining
  • People who have had major surgery within 4 weeks before joining, have not fully recovered from previous surgery, or who may need major surgery during the trial
  • People who have received radiotherapy within 2 weeks before joining, unless it was a short course given only to relieve symptoms
  • People with other significant medical conditions or other types of cancer

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 15 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: Ying Yuan, Prof., Second Affiliated Hospital, School of Medicine, Zhejiang University

Phone: +86-13805753262

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
Registry
ClinicalTrials.gov
Start date
1 April 2025
Est. completion
31 December 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Progression free survival

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: 15 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