Phase 2 Liver Cancer Trial, Recruiting NCT07544784 Sponsor: Fudan University Condition: Liver Cancer
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Phase 2 Liver Cancer Trial, Recruiting

NCT07544784
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 who have been confirmed through a tissue or cell sample to have colorectal cancer (bowel cancer)
  • People who have cancer that has spread to the liver, with at least one measurable area of cancer spread plus one liver tumour that can be treated with radiotherapy — but not people whose liver tumours were considered surgically removable from the start
  • People who have not yet received any treatment for their cancer, or people whose cancer has come back after surgery and who have not had any anti-cancer treatment in the past 6 months, with at least 6 months passed since their last course of chemotherapy after surgery
  • People who are generally well enough to carry out daily activities with little to no limitation (as rated on a standard medical scale of 0–1)
  • People who are expected to live for at least 3 months
  • People whose blood, liver, and kidney results fall within acceptable ranges on tests done within 7 days before screening — including healthy enough levels of red blood cells, white blood cells, and platelets; liver enzyme levels within acceptable limits; kidney function within acceptable limits; and blood clotting results within acceptable limits (confirm specific values with the trial site)
  • People who are willing to take part voluntarily, sign a consent form, and attend follow-up visits

Who may not be able to join:

  • People who have had another cancer in the past 3 years, except for certain fully treated skin cancers or cervical pre-cancers
  • People who have cancer that has spread to the brain or the lining of the brain and is causing symptoms, unless it has been treated and has been stable and symptom-free for more than 2 months
  • People who have a blocked bowel, active bowel bleeding, or a hole in the bowel wall
  • People who have previously been treated with certain immune checkpoint or T-cell targeting drugs (such as anti-PD-1, anti-PD-L1, or anti-CTLA-4 therapies)
  • People who have an active autoimmune disease, or a history of one that could return (such as lupus, rheumatoid arthritis, inflammatory bowel disease, multiple sclerosis, or similar conditions), or people at high risk due to organ transplant requiring immune-suppressing medication — though people with certain mild or well-controlled conditions (such as hypothyroidism on thyroid hormone replacement, type 1 diabetes on insulin, or vitiligo or psoriasis not needing systemic treatment in the past 2 years) may still be considered
  • People who currently have or have had lung inflammation, pulmonary fibrosis, or radiation-related lung disease
  • People who have taken part in another clinical drug trial within the past 4 weeks (observational studies without treatment are generally acceptable)
  • People who have taken immune-suppressing medications within the past 4 weeks, with some exceptions such as low-dose steroids, inhaled or topical steroids, or short-term steroids for allergies
  • People who have received a live vaccine (such as a live flu vaccine) in the past 4 weeks, or who plan to receive one during the trial — injected inactivated flu vaccines are generally acceptable
  • People who have had major surgery (such as brain, chest, or abdominal surgery) within the past 4 weeks, or who are expected to need major surgery during the trial
  • People who have HIV, other immune deficiency conditions, or who have had an organ or stem cell transplant
  • People with active hepatitis B or active hepatitis C — though carriers of hepatitis B who are stable on antiviral treatment, or people who have fully cleared hepatitis C, may be considered
  • People with active tuberculosis
  • People who have had a serious infection in the past 4 weeks, or an active infection requiring antibiotics in the past 2 weeks
  • People with moderate to severe heart failure or poorly controlled heart rhythm problems
  • People with high blood pressure that remains uncontrolled despite standard treatment (blood pressure of 160/100 mmHg or above)
  • People who have had a heart attack, stroke, unstable chest pain, or mini-stroke in the past 6 months
  • People who have had a serious blood clot (such as a deep vein clot or a clot in the lungs) in the past 3 months — minor clots related to medical lines or ports are generally not included in this
  • People with documented neurological or psychiatric conditions such as epilepsy, dementia, or peripheral nerve disorders
  • People with alcohol dependence or a history of drug misuse in the past year
  • People who are pregnant or breastfeeding, or people of childbearing potential who are not using adequate contraception
  • People with other significant medical, psychiatric, or laboratory abnormalities that the trial doctor believes would make participation unsafe or affect the trial results

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 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: +86-021-64175590

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
Registry
ClinicalTrials.gov
Start date
4 November 2025
Est. completion
1 December 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

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: 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