Phase 2 Colorectal Cancer Trial, Recruiting NCT06949111 Sponsor: Hebei Medical University Fourth Hospital Condition: Colorectal Cancer
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Phase 2 Colorectal Cancer Trial, Recruiting

NCT06949111
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:

  • Adults aged 18 or older, of any gender
  • People whose general health and ability to carry out daily activities meets a certain standard (rated 0 or 1 on a scale doctors use called the ECOG scale, meaning fully active or able to do light activity)
  • People who have been confirmed by a tissue biopsy to have a specific type of colon cancer called colon adenocarcinoma (including a variant called mucinous adenocarcinoma), and whose cancer has been tested and found to be a type called pMMR/MSS; the location of the cancer in the colon must also be clearly identified
  • People whose scans (CT or MRI with contrast) show the cancer is at a specific stage — spread into or through the bowel wall, but not to distant parts of the body (stage cT4, any lymph node involvement, no distant spread, based on AJCC 8th edition guidelines)
  • People whose blood test results before joining meet required levels for blood cell counts, liver and kidney function, and blood clotting (the trial site will assess this)
  • People who are able and willing to use effective contraception during the study and for 6 months after the last treatment (applies to women who could become pregnant and to men)
  • People who are willing to sign a consent form and commit to completing all treatment and follow-up appointments

Who may not be able to join:

  • People whose cancer is mainly (more than 50%) a different tumour type, such as neuroendocrine carcinoma or squamous cell carcinoma, rather than adenocarcinoma
  • People whose cancer has already spread to distant parts of the body, including the lining of the abdomen, lymph nodes outside the local area, or other organs
  • People who have already received radiotherapy, chemotherapy, targeted therapy, or immunotherapy for their colon cancer
  • People with active autoimmune diseases (such as lupus or rheumatoid arthritis) that require long-term medication to suppress the immune system
  • People with active serious infections, including HIV, or hepatitis B or C with a detectable virus level that requires ongoing antiviral treatment
  • People with serious heart or blood vessel conditions, such as a heart attack within the past 6 months, unstable chest pain, or blood pressure that cannot be controlled and is above 160/100 mmHg
  • People with a history of another cancer, unless it was a type of skin cancer (non-melanoma) or early-stage cervical cancer that was fully treated, and the person has been cancer-free for 5 years or more
  • People with poorly controlled diabetes (based on a blood sugar measure called HbA1c above 8%) or thyroid problems that require medication to manage
  • People with serious ongoing bowel conditions such as active Crohn's disease or ulcerative colitis
  • People with a history of bowel damage from previous radiation, or extensive internal scarring in the abdomen that would affect the ability to plan radiotherapy
  • People whose bone marrow function has not recovered, shown by low blood cell counts (the trial site will check blood results)
  • People with significant liver disease (rated Child-Pugh B or higher) or reduced kidney function below a certain level
  • People who are pregnant or breastfeeding (a pregnancy test is required during the screening process)
  • People with cognitive difficulties or a history of psychiatric conditions that may affect their ability to follow the treatment plan
  • People currently taking part in another interventional clinical trial
  • People whom the treating doctor considers unsuitable for the trial 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
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: 15032818011

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
Hebei Medical University Fourth Hospital
Registry
ClinicalTrials.gov
Start date
15 May 2025
Est. completion
1 February 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Tumor Complete Response (CR) 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