drugset / Trial / NCT03348514

Safety, Dose Tolerance, Pharmacokinetics, and Pharmacodynamics Study of CPX-POM in Patients With Advanced Solid Tumors

NCT03348514

Phase 1 Completed 19 enrolled CicloMed LLC Cmed Clinical Services · collab
Non-randomizedSequentialOpen-labelTreatment

Summary

This is a first-in-human, Phase I, multicenter, open label, dose escalation study to evaluate the DLTs and MTD and to determine the recommended Phase 2 dose (RP2D) of CPX-POM administered IV in patients with any histologically- or cytologically-confirmed solid tumor type.

Timeline

Start
2018-01-15
Primary completion
2020-05-31
Completion
2020-05-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Fosciclopirox Small molecule 30 mg/m2 Intravenous
Subject Fosciclopirox Small molecule 60 mg/m2 Intravenous
Subject Fosciclopirox Small molecule 120 mg/m2 Intravenous
Subject Fosciclopirox Small molecule 240 mg/m2 Intravenous
Subject Fosciclopirox Small molecule 360 mg/m2 Intravenous
Subject Fosciclopirox Small molecule 600 mg/m2 Intravenous
Subject Fosciclopirox Small molecule 900 mg/m2 Intravenous
Subject Fosciclopirox Small molecule 1200 mg/m2 Intravenous

Indications