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Clinical Trial · NCT06159049
Overview
Fibroblast activation protein (FAP) emerges as a highly promising target for cancer diagnostic imaging and targeted radionuclide therapy. To exploit the therapeutic potential of current FAP inhibitors (FAPIs), this study presented the design and synthesis of a series of FAPI dimers to increase tumor uptake and retention. Preclinical evaluation and a pilot clinical PET imaging study were conducted to screen the lead compound with the potential for radionuclide therapy.
Sponsor
Xiangya Hospital of Central South University
Contacts
Shuo Hu, Dr (STUDY_CHAIR)
ClinicalTrials.gov
NCT06159049Drug / Compound
Eligibility
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