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
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- POINT Biopharma, a wholly owned subsidiary of Eli Lilly and Company
- Principal Investigator
- Jessica JensenEli Lilly and Company
- Intervention
- [Ga-68]-PNT6555(drug)
- Enrollment
- 20 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2022 – 2024
Study locations (4)
- Memorial Sloan Kettering Cancer Center, New York, New York, United States
- University Health Network - Princess Margaret Cancer Centre, Toronto, Ontario, Canada
- CHUM - Centre hospitalier de l'Université de Montréal, Montreal, Quebec, Canada
- Jewish General Hospital, Montreal, Quebec, Canada
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.
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