drugset / Trial / NCT03545165
177Lu-J591 and 177Lu-PSMA-617 Combination for mCRPC
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |