Spots Global Cancer Trial Database for 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)
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Trial Identification
Brief 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)
Official 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)
Study ID: NCT05432193
Study Description
Brief Summary: 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.
Detailed Description:
Eligibility
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Locations
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, Montréal, Quebec, Canada
Jewish General Hospital, Montréal, Quebec, Canada
Contact Details
Name: Jessica Jensen
Affiliation: POINT Biopharma, a wholly owned subsidiary of Eli Lilly and Company
Role: STUDY_DIRECTOR
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