Phase 3 Lung Cancer Trial, Recruiting NCT06141070 Sponsor: Vastra Gotaland Region Condition: Lung Cancer
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Phase 3 Lung Cancer Trial, Recruiting

NCT06141070
Recruiting Phase 3

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:

  • You have agreed to take part and given written consent before any study procedures begin
  • You have been diagnosed with non-small cell lung cancer (NSCLC), confirmed by a tissue or cell sample
  • Your cancer is at stage IV (spread to other parts of the body) but has spread to 5 or fewer spots outside the main tumour and nearby lymph nodes
  • Your doctors consider you well enough to receive standard first-line cancer drug treatment (such as chemotherapy, immunotherapy, or a combination)
  • The cancer spots that have spread outside the chest area can be treated with a precise, targeted type of radiotherapy called SBRT
  • The tumour(s) in your chest can also be treated with SBRT or standard radiotherapy
  • You have not had any previous drug treatment or radiotherapy for this lung cancer (though previous treatment given after surgery for an earlier stage is allowed)
  • You are over 18 years old (there is no upper age limit)
  • You are generally well enough to carry out most daily activities (measured on a standard scale called WHO performance status 0–2)
  • Your major organs (such as kidneys, liver, and bone marrow) are working well enough for treatment
  • If you are a woman who could become pregnant, you have tested negative for pregnancy before joining
  • You are willing and able to attend all required appointments and follow-up visits throughout the study

Who may not be able to join:

  • Your cancer has spread only to a single spot in the brain, or only to the opposite lung, with no other distant spread
  • You have taken part in another clinical trial using an experimental treatment within the last 4 weeks
  • Your lung cancer has a specific genetic change (such as EGFR+, ALK+, or ROS1+) or any other gene alteration that means your standard treatment would be a targeted therapy pill (TKI), rather than chemotherapy or immunotherapy
  • You have cancer cells in fluid around your lungs or abdomen, or excessive fluid that would make the planned radiotherapy unsafe
  • The cancer has spread to the lining around the brain and spinal cord (leptomeningeal disease)
  • You have significant scarring in the lungs (pulmonary fibrosis) that would make the planned treatment too risky (minor findings on scans may still be acceptable — confirm with trial site)
  • You are not considered fit enough for standard first-line cancer drug treatment
  • You currently have, or have recently had, another type of cancer — some exceptions may apply, such as certain low-risk or previously treated cancers; confirm details with the trial site
  • You are pregnant, breastfeeding, or are unwilling to use reliable contraception from the start of the study until 90 days after your last dose of treatment (applies to both men and women of reproductive age)
  • You have any other medical condition that, in the opinion of the study doctor, could affect your safety or interfere with the study results (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 13 July 2026
Phase 3: approximately ~65% 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: +46313427954

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 3
Sponsor
Vastra Gotaland Region
Registry
ClinicalTrials.gov
Start date
1 December 2023
Est. completion
1 December 2028

Where this trial is recruiting

🇸🇪 Sweden

Primary endpoints

Overall survival (OS)

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: 13 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