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Clinical Trial 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).


Clinical Trial Description

n/a


Study Design

Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Health Services Research


Related Conditions & MeSH terms


NCT number NCT00543075
Study type Interventional
Source Genta Incorporated
Contact
Status Completed
Phase Phase 1
Start date May 2006
Completion date September 2009

See also
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Completed NCT04656795 - PK Study in Subjects With Renal Impairment (Severe and if Required Mild & Moderate) Compared to Subjects With Normal Renal Function Phase 1
Completed NCT02965040 - A Phase 1 Study of Roxadustat in Subjects With Different Degrees of Renal Function Phase 1