About this trial
c-MET is a receptor tyrosine kinase overexpressed in multiple malignancies and associated with tumor progression, therapeutic resistance, and poor prognosis, while showing limited expression in normal tissues, making it an attractive imaging and therapeutic target. Current assessment relies on invasive biopsy and is limited by tumor heterogeneity and sampling bias.
FL-261 is a novel c-MET-targeting ligand with high affinity and specificity, favorable tumor uptake and retention, rapid background clearance, and good preclinical safety. It can be radiolabeled for both diagnostic imaging and potential theranostic applications.
This first-in-human study will evaluate \[68Ga\]Ga-FL-261 PET or \[111In\]In-FL-261 SPECT imaging in patients with advanced malignancies, including non-small cell lung cancer, colorectal cancer, and head and neck cancer. The study aims to assess safety, biodistribution, and tumor-targeting capability, and to explore its diagnostic value by correlating imaging findings with histopathological c-MET expression.
Eligibility criteria
Qualifiers
Ability to provide written informed consent (by the subject or legally authorized representative)
Willingness and ability to comply with all study procedures
Age ≥18 years, any sex
Clinically suspected or histologically confirmed malignancies (e.g., non-small cell lung cancer, colorectal cancer, head and neck cancer), supported by tumor markers, imaging (ultrasound, CT, MRI), or pathology
Disqualifiers
Inability or unwillingness to provide informed consent
Inability to comply with study procedures
Acute systemic disease or significant electrolyte imbalance
Pregnant or breastfeeding women
Trial design
Treatments tested in this trial
- [68Ga]Ga-FL-261 PET Imaging / [111In]In-FL-261 SPECT Imaging