Lung Cancer Trial, Recruiting NCT05754203 Sponsor: Xinqiao Hospital of Chongqing Condition: Lung Cancer
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Lung Cancer Trial, Recruiting

NCT05754203
Recruiting Not Applicable

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:

  • A person must have read, understood, and signed a consent form, and the trial doctor must judge them able to follow the study's requirements.
  • A person must have been diagnosed with stage IIIB or higher non-small cell lung cancer, confirmed by a tissue biopsy or similar test (whether newly diagnosed or previously diagnosed).
  • The cancer tumour must be small enough to be treated with a precise, focused type of radiotherapy called SBRT (less than 5 cm in size) and must also be suitable for immune checkpoint inhibitor treatment, based on established cancer treatment guidelines.
  • A person must be aged 18 or older and under 75.
  • A person must have a physical fitness/ability-to-function score (called ECOG PS) of between 0 and 3, meaning they can carry out at least some daily activities (confirm with trial site for exact score requirements).

Who may not be able to join:

  • People who are unlikely to follow the study rules or who have previously not complied with trial requirements.
  • People with significant problems affecting the liver, kidneys, or heart, such as a past heart attack, ongoing chest pain (angina), or notably raised liver enzyme levels.
  • People who have needed to take corticosteroid medications or other drugs that suppress the immune system within the 14 days before joining.
  • People who had a serious infection in the 4 weeks before joining, including infections serious enough to require a hospital stay, bloodstream infections, or severe pneumonia.
  • People who have needed oral or intravenous antibiotics for a severe ongoing or active infection (including tuberculosis) in the 14 days before joining.
  • People with untreated chronic hepatitis B, or hepatitis B carriers whose virus levels are at or above 500 IU/mL, or people with currently active hepatitis C. Note: People with inactive hepatitis B, treated and stable hepatitis B (with virus levels below 500 IU/mL), or fully cleared hepatitis C may still be considered eligible (confirm with trial site).
  • People with a known history of HIV infection.
  • People who have taken part in another clinical trial or received an experimental treatment within the 28 days before joining.
  • People who have a medical reason that would make either the focused radiotherapy (SBRT) or the immune checkpoint inhibitor treatment unsafe for them (confirm with trial site).

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 21 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Jianguo Sun, Department of Oncology, Xinqiao Hospital, Army Medical University

Phone: +862368774490

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
Not Applicable
Sponsor
Xinqiao Hospital of Chongqing
Registry
ClinicalTrials.gov
Start date
1 August 2023
Est. completion
1 March 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

objective response 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: 21 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