Phase 2 Colorectal Cancer Trial, Recruiting NCT06254521 Sponsor: First Affiliated Hospital of Guangxi Medical University Condition: Colorectal Cancer
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Phase 2 Colorectal Cancer Trial, Recruiting

NCT06254521
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 aged 18 to 70 years old.
  • People who have been diagnosed with a specific type of colon cancer called MSS colon adenocarcinoma, confirmed through laboratory testing (either genetic testing or tissue staining methods).
  • People whose tumor is located less than 12cm from the anal opening, as measured by colonoscopy, MRI, or rectal ultrasound.
  • People whose cancer imaging (MRI or rectal ultrasound) shows the tumor has grown to a certain depth into or through the bowel wall (stage T3–T4) or has spread to nearby lymph nodes (N+), but has not spread to other parts of the body (M0 on CT scan).
  • People with a good general physical condition, rated 0 or 1 on a standard medical fitness scale (confirm with trial site).
  • People with a life expectancy of more than one year.
  • People who have been newly diagnosed, have not received any previous cancer treatment, and have no medical reasons preventing chemotherapy.
  • People whose blood counts and organ function (including liver and kidney) meet specific healthy levels as defined by the trial (confirm with trial site for exact values).
  • People who are willing and able to understand the study and provide written consent to participate.

Who may not be able to join:

  • People with early-stage rectal cancer (T1–T2, no lymph node involvement, no spread), or people whose tumor is less than 5cm from the anal opening and classified as T4, where a specific type of major surgery (removal of the rectum and anus) would be needed.
  • People with cancer occurring in multiple locations in the bowel at the same time.
  • People whose tumor is causing a blockage, severe bleeding, or risk of bowel perforation that requires emergency surgery or a stent.
  • People who are unable to tolerate chemotherapy or immunotherapy — for example, due to very low blood cell counts.
  • People with a history of another cancer, except for certain low-risk cancers such as basal cell skin cancer, a specific type of thyroid cancer, or cancers that were entirely contained and not invasive.
  • People experiencing a severe flare-up of a serious ongoing condition (such as lung disease, heart disease, or kidney problems) or a severe active infection (such as hepatitis, pneumonia, or heart inflammation), or those rated above 3 on a standard surgical risk scale (confirm with trial site).
  • People with mental health conditions, inability to read, or communication difficulties that would prevent understanding of the study.
  • People with existing nerve damage in their hands or feet that would prevent them from receiving a specific chemotherapy drug (oxaliplatin).
  • People who have used steroid medications (glucocorticoids) continuously for more than 3 days in the month before signing the consent form, or who need ongoing steroid treatment for another condition.
  • People who are unable to have a contrast-enhanced CT scan.
  • People who are pregnant or breastfeeding.
  • People who have declined to take part in the study.
  • People whom the research team considers 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 23 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

Principal Investigator: Hui Li, Professor, First Affiliated Hospital of Guangxi Medical University

Phone: 13407738560

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
First Affiliated Hospital of Guangxi Medical University
Registry
ClinicalTrials.gov
Start date
22 February 2024
Est. completion
30 December 2024

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Pathological complete response (pCR) rate

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