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FAPi Radioligand OpeN-Label, Phase 1 Study to Evaluate Safety, Tolerability and DosImetry of [Lu-177]-PNT6555; A Dose Escalation Study for TReatment of Patients With Select Solid Tumors (FRONTIER)

POINT Biopharma, a wholly owned subsidiary of Eli Lilly and Company · 2022
ClinicalTrials.gov · Datasets · License: Public Domain · 2022
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cholangiocarcinomacolorectal-canceresophageal-cancerhead-and-neck-squamous-cell-carcinomamelanoma-skinpancreatic-ductal-adenocarcinomasoft-tissue-sarcoma
This Phase 1 study will evaluate the safety and tolerability of \[Ga-68\]-PNT6555 and \[Lu-177\]-PNT6555 in subjects with select solid tumors that have FAP over-expression, in order to determine a recommended Phase 2 dose.
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