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This PET imaging trial will compare two promising T cell PET tracers alongside the pathological analysis of the resected tumor. Following chemo-immunotherapy, NSCLC patients will undergo two PET scans shortly before their surgery.
This study explores tumoral uptake of [18F]F-AraG and its association with the treatment effect of immune checkpoint inhibitors for stage 4 NSCLC patients. [18F]F-AraG PET/CT scanning will be performed twice per patient, pre and post start of immunotherapy. The uptake difference in tumor and associated lymphoid organs will be considered for the analysis, as well as the correlation with the expression of CD8, PD-1 and Treg markers in immunohistochemistry. CellSight is providing [18F]F-AraG precursor free of charge.
This pilot study uses [18F]F-AraG PET imaging to evaluate the immunological response to inhibitor therapy (CkIT) in patients with advanced NSCLC tumors.
This pilot study aims to evaluate the test-retest variability of [18F]F-AraG-PET imaging in patients with advanced NSCLC tumors.
The aim of the SHARP trial is to investigate changes in [18F]F-AraG uptake following Anti-PD-1 therapy in patients with non-small cell lung cancer (NSCLC).
In this study, patients with advanced solid tumors will undergo [18F]F-AraG PET/CT imaging to assess for changes in tracer uptake following treatment with CkIT.
In this pilot study, healthy volunteers and patients with Non-Small Cell Lung Cancer will undergo [18F]F-AraG dynamic imaging on the uEXPLORER total body PET/CT scanner to obtain preliminary data regarding pharmacokinetics and early biodistribution images.
This is a pilot study using [18F]F-AraG PET imaging to evaluate the immunological response to checkpoint inhibitor therapy (CkIT) in patients with advanced NSCLC tumors at multiple study sites.
This is a single arm exploratory imaging study involving up to two intravenous microdoses of [18F]F-AraG (the second tracer dose is optional) followed by whole-body PET-CT imaging in participants with convalescent COVID-19.
This is a pilot study in adult subjects with aggressive B-cell lymphoma who will receive commercial or research CAR T cell therapy as anticancer treatment.
The aim of the ATTAIN trial is to investigate the pharmacokinetic characteristics of [18F]F-AraG by performing a full kinetic modelling, assess test-retest (TRT) variability and to correlate the tumor tracer uptake with the pathological assessment.
This study involves one intravenous microdose of [18F]F-AraG followed by whole-body positron emission tomography-magnetic resonance (PET-MR) imaging in HIV infected individuals to determine the anatomical distribution of the PET tracer.
This is a prospective clinical trial in patients with non-small cell lung cancer (NSCLC) undergoing PD-1/PD-L1-directed therapy. This research is being done to find out if [18F]F-AraG is a helpful imaging agent for detecting changes in cancer's anti-tumor immune response levels for NSCLC patients who will receive a cancer immunotherapy regimen.
The main goal of this research study is to determine how nivolumab and nivolumab/Vidutolimod (CMP-001) combination affect the likelihood of destroying melanoma involving lymph node and/or in-transit/satellite areas.
This study is to assess the biodistribution and kinetics of [18F]F-AraG in non-small cell lung cancer patients undergoing immunotherapy with and without adjuvant radiation therapy.
This study determines the utility of in vivo imaging with [18F]F-AraG to identify sites of Graft Versus Host Disease (GVHD) in patients highly suspected of having acute GVHD who require systemic therapy, and patients at high risk for developing acute GVHD.
This phase II trial studies how well [18F]F-AraG PET/MR imaging works in measuring clinical response to atezolizumab or patients with cancer receiving standard of care Anti-PD-1/L1.
This is a cross-sectional imaging and correlative biomarker study in patients with Squamous Cell Carcinoma of the Head and Neck (SCCHN). Two whole body PET/CT images with [18F]F-AraG, blood samples, and tissue biopsies will be collected from patients.
This is a Phase 1 study is to visualize biodistribution of [18F]F-AraG (VisAcT) in cancer patients expected to undergo immunotherapy and/or radiation therapy.
The goal of this study is to visualize biodistribution of [18F]F-AraG through time in healthy human volunteers.