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A Single Dose Study Investigating the Elimination as Well as the Tolerability of PD 0332334 in Healthy Subjects as Compared to Patients With Impaired Kidney Function.

Pharmacokinetics Clinical Trial

Official title:
A Phase 1, Open-Label, Single Dose Study To Evaluate The Pharmacokinetics, Safety, And Tolerability Of PD 0332334 In Subjects With Various Degrees Of Renal Function

Clinical Trial Summary

1. To investigate the effect of kidney function on the elimination of a single dose of PD 0332334 from the body.

2. To investigate the safety and tolerability of a single dose of PD 0332334 in patients with impaired kidney function.

Clinical Trial Description

Additional Study Purpose Details: Investigation of the pharmacokinetics, safety, and tolerability of a single dose of PD 0332334 in patients with impaired renal function.

On February 23rd 2009, a decision to terminate further development for PD 0332334 was communicated to investigators in this study. The decision to terminate this study was not based on any safety concerns. ;

Study Design

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

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00721422
Study type Interventional
Source Pfizer
Contact
Status Terminated
Phase Phase 1
Start date August 2008
Completion date February 2009
View Details
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