Phase 1 Lung Cancer Trial, Recruiting
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 unresectable (cannot be surgically removed) Stage IIIB, IIIC, or Stage IV squamous cell lung cancer, confirmed by a tissue or cell sample test
- People whose cancer tests positive for a protein called GPC3, as measured by a specific lab test done at a central laboratory
- People whose cancer has continued to grow or who could not tolerate up to three previous treatment regimens for advanced or metastatic squamous cell lung cancer
- People who have at least one tumour that can be measured on scans
- People whose heart pumping function (measured by an echocardiogram) is at 50% or above and is reported as normal
- People who have adequate lung function
- People whose blood test results meet the study's required levels
- Female participants of childbearing potential who test negative for pregnancy, and all non-sterilised participants (male and female) who agree to use effective contraception for at least 12 months and until the CAR-T cells are no longer detectable in the body after the infusion
Who may not be able to join:
- People whose cancer has a specific genetic mutation for which a targeted standard treatment is already recommended under local treatment guidelines
- People with known serious allergies or intolerances to the CAR-T cell product or any of its ingredients, including a substance called DMSO
- People who have medical reasons preventing them from receiving the preparatory chemotherapy drugs (fludarabine and/or cyclophosphamide) used before the CAR-T treatment
- People who have had their spleen removed or have had an organ transplant
- People who have previously received any CAR-T cell therapy, or any treatment specifically targeting the GPC3 protein
- People with uncontrolled or ongoing serious lung disease
- People with a clinically significant build-up of fluid in the abdomen
- People with uncontrolled fluid build-up around the lungs or heart that requires repeated draining procedures
- People with cancer that has spread to the spinal cord, the lining of the brain or spinal cord, or the brain
- People who have received radiation therapy, certain local treatments, vaccines, blood transfusions, or systemic treatments within specific time periods before the cell collection procedure, as defined by the study protocol
- People with a history of, or currently active, certain medical conditions or diseases as defined in the study protocol (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.
Contact this trial
Principal Investigator: Shun Lu, MD, Shanghai Chest Hospital, China
Phone: +86-18616644879
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
Where this trial is recruiting
Primary endpoints
AE/SAE/AESI, DLT
Can't join this trial?
Data last synced from ClinicalTrials.gov: 14 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.