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CompletedNCT01419041

A Study to Evaluate The Pharmacokinetics Of Crizotinib (PF-02341066) In Subjects With Impaired Renal Function

A Phase I, Single Dose, Parallel-Group Study To Evaluate The Pharmacokinetics Of Crizotinib (PF-02341066) In Subjects With Impaired Renal Function

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
16 (actual)
Sponsor
Pfizer · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Accepted

Summary

The present study is being conducted to evaluate whether or not severe renal impairment has an effect on crizotinib Pharmacokinetics.

Conditions

Interventions

TypeNameDescription
DRUGcrizotinibSingle-dose oral 250 mg crizotinib in subjects with normal renal function (CLcr =\>90 mL/min)
DRUGcrizotinibSingle-dose oral 250 mg crizotinib in subjects with severe renal impairment (CLcr \<30 mL/min)

Timeline

Start date
2011-11-01
Primary completion
2012-08-01
Completion
2012-08-01
First posted
2011-08-17
Last updated
2012-10-01

Locations

3 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT01419041. Inclusion in this directory is not an endorsement.

A Study to Evaluate The Pharmacokinetics Of Crizotinib (PF-02341066) In Subjects With Impaired Renal Function (NCT01419041) · Clinical Trials Directory