An Phase I Trial of a CAR T-cell Infusion C-CAR031 in Participants With GPC3+ Advanced/Metastatic Squamous Cell Lung Cancer
Recruiting · NCT07444281 · Interventional (participants receive a specific treatment) · Lead sponsor: Shanghai AbelZeta Ltd.
View the official record on ClinicalTrials.gov →Interventions studied
C-CAR031
What this trial is about
This single-arm, open-label, multicenter, Phase I study will evaluate the safety, tolerability, anti-tumor activity, pharmacokinetics (PK)/pharmacodynamics (PD), biomarker, and immunogenicity of C-CAR031 in adult participants with GPC3+ advanced/metastatic squamous cell lung cancer, who are not amenable to curative therapy and have progressed or are intolerant to no more than 3 lines of prior systemic treatment including immune checkpoint inhibitors (CPIs) and platinum-based doublet chemotherapy, concurrently or sequentially.
Who can take part
Age range
18 Years to 75 Years
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Phase 1
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- Histologically or cytologically confirmed unresectable Stage IIIB ,IIIC or IV squamous cell lung cancer
- Confirmed to express GPC3, as assessed by immunohistochemistry at a central lab
- Participants who have progressed or intolerant to no more than three lines of prior systemic therapies for advanced/metastatic squamous cell lung cancer
- At least one measurable target lesion
- The left ventricular ejection fraction (LVEF) measured by echocardiography ≥50% and reported as non-impaired.
- Sufficient pulmonary function
- The laboratory testing results meet the study requirements
- Female participants of childbearing potential must test negative for pregnancy in serum or urine. Non-sterilized participants (males and females) agree to take effective contraceptive measures for at least 12 months and until CAR-T below lower limit of detection (LLOD) by PCR which occurs last after C-CAR031 infusion.
Exclusion criteria
- known to harbor a driver mutation for which targeted standard therapy is recommended in accordance with local treatment guidelines.
- Known life-threatening allergies, hypersensitivity, or intolerance to the CAR-T product or its excipients, including dimethyl sulfoxide (DMSO)
- Contraindication to lymphodepleting agents, including fludarabine and/or cyclophosphamide.
- History of splenectomy or organ transplantation
- Prior treatment with Any CAR-T therapy OR any therapy that is targeting GPC3
- Uncontrolled or intercurrent pulmonary disease
- Clinically meaningful ascites
- Uncontrolled pleural effusion or pericardial effusion requiring recurrent drainage procedures
- Cancer-related spinal cord compression, leptomeningeal disease, or brain metastases
- Received radiation therapy, local treatment, vaccine, blood transfusion, systemic treatment within certain period of apheresis required by study protocol
- History of or with active diseases or conditions of that's defined in study protocol
Where it is running
1 location listed.
- Shanghai Chest Hospital - Shanghai, Shanghai Municipality, China