Phase 2 Lung Cancer Trial, Recruiting NCT06455917 Sponsor: University Hospital, Basel, Switzerland Condition: Lung Cancer
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Phase 2 Lung Cancer Trial, Recruiting

NCT06455917
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 are able to understand the study's purpose, agree to take part by signing a consent form, and are willing and able to follow the study procedures.
  • People who are 18 years of age or older.
  • People whose cancer-related physical functioning is rated at a level where they are either fully active or have only minor limitations in physical activity (ECOG score of 0 or 1).
  • People whose non-small cell lung cancer (a type of lung cancer) has been confirmed through laboratory testing of tissue samples.
  • People whose cancer has continued to grow or spread after at least one standard treatment, and where no approved treatment aimed at curing the cancer is available.
  • People who have a tumor or spread of cancer (metastasis) in a location that can be surgically reached for tissue collection.
  • People who are willing to undergo a surgical procedure, such as a removal or biopsy, to collect one or more tumor samples.
  • People whose heart, lungs, blood, liver, and kidneys are functioning at an adequate level, as assessed by the treating doctor. People aged 50 or older, or those with existing heart conditions, will also need to complete a cardiac stress test.
  • Women who could potentially become pregnant, who are approaching menopause, or who have been in menopause for less than two years, must have a negative blood pregnancy test before joining.

Who may not be able to join:

  • People with active cancer that has spread to the brain or spinal cord. People whose brain or spinal cord metastases have been treated and have been stable for at least one month may still be considered.
  • People who currently have a second active cancer.
  • People with significant, uncontrolled other medical conditions that could affect their ability to follow the study — including autoimmune disorders, conditions affecting immune function, serious lung disease, or serious heart or blood vessel disease, as determined by the treating doctor.
  • People who have previously had serious side effects from immune-based cancer treatments that would prevent them from safely receiving similar treatments again, as determined by the treating doctor.
  • People currently taking medications that suppress the immune system in a way that would interfere with the study treatments, as determined by the treating doctor.
  • People with severe active infections or infections that are not under control and require treatment.
  • People with any other medical conditions, allergies, or health findings that would make it unsafe to receive any of the treatments used in the study.
  • People for whom any of the planned procedures or treatments are otherwise medically unsuitable.
  • Women who are pregnant, breastfeeding, or not willing to use a highly effective method of contraception throughout the study period.
  • People with a known allergy or sensitivity to any of the study treatments or to substances used in the preparation of the therapy.
  • People who are known to have HIV, or who test positive for HIV during screening.
  • People with a known hepatitis B or hepatitis C infection.

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 22 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: David König, Dr. med., University Hospital, Basel, Switzerland

Phone: +41 61 265 5074

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
University Hospital, Basel, Switzerland
Registry
ClinicalTrials.gov
Start date
22 January 2025
Est. completion
1 December 2029

Where this trial is recruiting

🇨🇭 Switzerland

Primary endpoints

Progression-free rate at 6 months after Tumor-infiltrating lymphocytes transfer.

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: 22 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