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