Phase 2 Lung Cancer Trial, Recruiting NCT06778382 Sponsor: Shandong Cancer Hospital and Institute Condition: Lung Cancer
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Phase 2 Lung Cancer Trial, Recruiting

NCT06778382
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 diagnosed with colorectal cancer confirmed by a pathology test, and whose cancer is no longer detectable (called "No Evidence of Disease" or NED) after treatment such as surgery, ablation, or radiotherapy.
  • People who have maintained NED status for at least 6 months.
  • People who have either received no chemotherapy, or have only received chemotherapy after surgery or as a first course of treatment.
  • People who, after at least 6 months of NED, have developed a small number of lung spots (5 or fewer), which doctors consider suitable for a targeted destructive treatment.
  • People who have never had radiotherapy to the lungs before.
  • People who have at least one measurable tumour spot of a minimum size, as defined by standard imaging measurement guidelines (confirm with trial site for exact size details).
  • People whose general physical functioning is rated at 2 or below on a standard medical scale, meaning they are able to carry out basic daily activities, even if some help is needed.
  • People whose doctors expect them to live for at least 3 months or more.
  • People whose blood counts are at an adequate level, specifically a type of white blood cell (neutrophils) count of at least 1.6 x 10⁹/L, without needing medication to boost blood cell production for at least 7 days before testing.
  • People whose liver, kidneys, lungs, and heart are functioning well enough to safely receive at least one of the targeted treatments offered in this trial, as assessed by a treating doctor.
  • Women who could become pregnant must agree to use a reliable form of contraception from the time of signing consent until 1 year after treatment ends.
  • People who have voluntarily agreed to take part and provided written informed consent.

Who may not be able to join:

  • People whose colorectal cancer was first diagnosed already at an advanced or widespread (metastatic) stage.
  • People who have more than 5 lung spots, or who have cancer that has spread to the liver, bones, or lymph nodes.
  • People whose lung spots are not considered suitable for radiotherapy, as determined by the trial doctors.
  • People who have previously received a second or later course of systemic (whole-body) cancer treatment.
  • People whose liver or kidney function test results are significantly above the normal range (confirm with trial site for exact values).
  • People with a CEA tumour marker blood level of 50 ng/mL or higher (CEA is a protein sometimes elevated in colorectal cancer).
  • People with serious ongoing health conditions that could interfere with the study, such as uncontrolled diabetes, stomach ulcers, or severe heart or lung disease, as judged by the research team.
  • People with a severe or uncontrolled infection.
  • People with an active autoimmune disease (a condition where the immune system attacks the body's own tissues).
  • People with significant problems affecting the brain or nervous system.
  • People who have had major surgery (other than a lymph node biopsy) within the past 30 days.
  • Women who are pregnant, breastfeeding, or of childbearing age and not using contraception.
  • People who are known to be allergic to any of the treatments used in this trial.
  • People who the research team determine are unsuitable 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 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

Principal Investigator: Jinbo Yue, Dorcter, Shandong Cancer Hospital and Institute

Phone: 0531-67626442

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
Shandong Cancer Hospital and Institute
Registry
ClinicalTrials.gov
Start date
24 June 2024
Est. completion
1 November 2025

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Time Without Systemic Therapy

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