drugset / Trial / NCT01278758

A Dose-escalation Pharmacokinetic Study of Intravenous ASA404 in Adult Advanced Cancer Patients With Impaired Renal Function and Patients With Normal Renal Function

NCT01278758

Phase 1 Terminated 7 enrolled Novartis Pharmaceuticals
NaParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety and pharmacokinetics of ASA404 in patients with refractory or relapsed metastatic cancer with impaired renal function and with normal renal function. It is very possible that patients with renal impairment will show differences in renal excretion of parent ASA404 and its metabolites, warranting a study that leads to a better pharmacokinetic assesssment in this population.

Timeline

Start
2010-03
Primary completion
2010-11
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject ASA404 Unknown Intravenous