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Clinical Trial Summary

A study to compare a 48-hour continuous infusion of conivaptan in subjects with mild and moderate liver impairment versus subjects with normal liver function


Clinical Trial Description

n/a


Study Design

Allocation: Non-Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Parallel Assignment, Masking: Open Label


Related Conditions & MeSH terms


NCT number NCT00851227
Study type Interventional
Source Cumberland Pharmaceuticals
Contact
Status Completed
Phase Phase 1
Start date February 2009
Completion date January 2010

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