drugset / Trial / NCT04525131

Safety, Dose Tolerance, Pharmacokinetics, Pharmacodynamics of CPX-POM in Patients With Newly Diagnosed or Recurrent Bladder Tumors

NCT04525131

Phase 2 Completed 12 enrolled CicloMed LLC
NaSingle-groupOpen-labelTreatment

Summary

This is a phase II, single center open label to determine safety, dose tolerance, PK and PD of the recommended Phase 2 dose (RP2D) of CPX-POM administered in patients with any newly diagnosed or recurrent bladder tumors.

Timeline

Start
2020-11-25
Primary completion
2022-12-30
Completion
2023-06-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Fosciclopirox Small molecule 900 mg/m2 Intravenous