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A Pharmacokinetics and Safety Study of Naproxcinod in Subjects With Impaired Renal Function — HCT3012-X-106  

Renal Failure Clinical Trial

Official title:
A Phase 1 Repeated Dose Open Label Study to Investigate the Pharmacokinetics and Safety of Naproxcinod 750mg Bid Administered to Patients With Impaired Renal Function Compared to Matching Healthy Subjects

Clinical Trial Summary

To study the pharmacokinetics and safety of naproxcinod in patients with impaired renal function

Clinical Trial Description

This is an 8-day, repeated dose, open label study to investigate the pharmacokinetics and safety of naproxcinod in order to guide initial dosing and achieve the optimal dose of naproxcinod in Renal impaired patients. ;

Study Design

Allocation: Non-Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00674856
Study type Interventional
Source NicOx
Contact
Status Completed
Phase Phase 1
Start date May 2008
Completion date October 2008
View Details
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