drugset / Trial / NCT03545165

177Lu-J591 and 177Lu-PSMA-617 Combination for mCRPC

NCT03545165

Phase 1/2 Terminated 6 enrolled Weill Medical College of Cornell University
NaSingle-groupOpen-labelTreatment

Summary

Phase I dose escalation study with combination of 177Lu-J591 and 177Lu-PSMA-617 using a dose-fractionated regimen will be performed in patients with documented progressive metastatic CRPC. The cumulative 177Lu-J591 dose for each subject will be 2.7 GBq/m2 (73 mCi/m2) of 177Lu with 20 mg J591 and the cumulative 177Lu-PSMA-617 dose for each subject will vary (depending on the Cohort) from 3.7 GBq (100 mCi) to 18.5 GBq (500 mCi). The 177Lu-PSMA-617 dose will be escalated in up to 6 different dose levels (3+3 dose-escalation study / de-escalation design). For the phase II portion, a minimum number of 14 patients will be enrolled at MTD (including those enrolled at MTD in Phase I) and a maximum of 24.

Timeline

Start
2018-04-18
Primary completion
2020-07-15
Completion
2020-07-15

Drugs

EvaluationDrugModalityDoseRoute
Subject 177Lu-PSMA-617 Other / unclassified 1850 mbq Intravenous
Subject 177Lu-PSMA-617 Other / unclassified 3700 mbq Intravenous
Subject 177Lu-PSMA-617 Other / unclassified 5550 mbq Intravenous
Subject 177Lu-PSMA-617 Other / unclassified 7400 mbq Intravenous
Subject 177Lu-PSMA-617 Other / unclassified 9250 mbq Intravenous
Subject 68Ga-PSMA-11 Diagnostic / imaging agent 185 mbq Intravenous
Background J591 177LU Monoclonal antibody 1.35 unknown Intravenous

Indications