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Clinical trial

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)

NCT05432193 is registered in ClinicalTrials.gov with POINT Biopharma, a wholly owned subsidiary of Eli Lilly and Company as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
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)
Lead sponsor
POINT Biopharma, a wholly owned subsidiary of Eli Lilly and Company
Phase
Phase 1
Overall status
Terminated
Start date
July 13, 2022
Completion date
October 2, 2024
Enrollment
20 (actual)
Sites
4

Conditions

As the registry lists them; a condition with its own page is linked.

cholangiocarcinoma, colorectal cancer, esophageal cancer, head and neck squamous cell carcinoma, melanoma (skin), pancreatic ductal adenocarcinoma, soft tissue sarcoma