drugset / Trial / NCT00543075

Pharmacokinetic Study of Genasense in Subjects With Normal Renal Function, Mildly Impaired Renal Function, and Moderately Impaired Renal Function

NCT00543075

Phase 1 Completed 23 enrolled Genta Incorporated
Non-randomizedSingle-groupOpen-labelHealth-services research

Summary

To characterize the pharmacokinetics of G3139 in subjects with normal, mildly impaired, and moderately impaired renal function who receive Genasense 3 mg/kg/day by continuous intravenous infusion for 2 days (48 hours).

Timeline

Start
2006-05
Primary completion
2007-11
Completion
2009-09

Drugs

EvaluationDrugModalityDoseRoute
Subject oblimersen sodium Antisense oligonucleotide 3 mg/kg Intravenous