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Clinical Trial Summary

The study is designed to evaluate the pharmacokinetics, safety and tolerability, immunogenicity and pharmacogenetics of a single dose of serelaxin/RLX030 in patients with severe renal impairment and end-stage-renal-disease (ESRD) compared to healthy volunteers.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01875523
Study type Interventional
Source Novartis
Contact
Status Completed
Phase Phase 1
Start date August 2013
Completion date December 2013

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