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Clinical Trial Details

Trial ID: L4695
Source ID: NCT01369602
Associated Drug: Pf-04991532
Title: Study To Evaluate The Effect Of Renal Impairment On The Pharmacokinetics Of PF-04991532
Acronym:
Status: COMPLETED
Study Results: NO
Results:
Conditions: Type 2 Diabetes Mellitus|Healthy
Interventions: DRUG: PF-04991532|DRUG: PF-04991532|DRUG: PF-04991532|DRUG: PF-04991532
Outcome Measures: Primary: Area under the plasma concentration versus time curve (AUClast), 0, 0.5, 1, 2, 3, 4, 5, 6, 8, 10, 12, 16, 24, 36, 48 hrs|Maximum observed plasma concentration (Cmax), 0, 0.5, 1, 2, 3, 4, 5, 6, 8, 10, 12, 16, 24, 36, 48 hrs|Time of maximum observed plasma concentration (Tmax), 0, 0.5, 1, 2, 3, 4, 5, 6, 8, 10, 12, 16, 24, 36, 48 hrs|Renal Clearance (Clr), 0 to 24 hours|Amount of drug excreted (Ae), 0 to 24 hours |
Sponsor/Collaborators: Sponsor: Pfizer
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE1
Enrollment: 27
Study Type: INTERVENTIONAL
Study Designs: Allocation: NON_RANDOMIZED|Intervention Model: PARALLEL|Masking: NONE|Primary Purpose: BASIC_SCIENCE
Start Date: 2011-07
Completion Date: 2012-02
Results First Posted:
Last Update Posted: 2012-02-22
Locations: Pfizer Investigational Site, Anaheim, California, 92801, United States|Pfizer Investigational Site, DeLand, Florida, 32720, United States
URL: https://clinicaltrials.gov/show/NCT01369602