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

PHASE1CompletedINTERVENTIONAL
Enrollment

23

Participants

Timeline

Start Date

May 31, 2006

Primary Completion Date

November 30, 2007

Study Completion Date

September 30, 2009

Conditions
Normal Renal FunctionMildly Impaired Renal FunctionModerately Impaired Renal Function
Interventions
DRUG

Genasense (oblimersen, G3139)

3 mg/kg/day by intravenous infusion for up to 48 hours

Trial Locations (1)

55404

DaVita Clinical Research, Minneapolis

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Genta Incorporated

INDUSTRY