TerminatedPhase 1NCT05432193

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)

Studying Cholangiocarcinoma

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Key facts

Sponsor
POINT Biopharma, a wholly owned subsidiary of Eli Lilly and Company
Principal Investigator
Jessica Jensen
Eli Lilly and Company
Intervention
[Ga-68]-PNT6555(drug)
Enrollment
20 enrolled
Eligibility
18 years · All sexes
Timeline
20222024

Study locations (4)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT05432193 on ClinicalTrials.gov

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