Status:
COMPLETED
A Study To Evaluate The Effect Of Food On How Tasocitinib (CP-690,550) Is Absorbed And Moves Through The Body Following Oral Administration Of Tasocitinib (CP-690,550) Tablets To Healthy Subjects
Lead Sponsor:
Pfizer
Conditions:
Rheumatoid Arthritis
Eligibility:
All Genders
21-55 years
Phase:
PHASE1
Brief Summary
In this study, a 10 mg tasocitinib (CP-690,550) tablet will be administered to healthy subjects on two separate dosing occasions. On one occasion the tasocitinib (CP-690,550) tablet will be administer...
Detailed Description
To evaluate the effect of food on the pharmacokinetics of tasocitinib (CP-690,550).
Eligibility Criteria
Inclusion
- Healthy male and/or female (non-childbearing potential) subjects between the ages of 21 and 55 years.
- Body Mass Index (BMI) of 17.5 to 30.5 kg/m2; and a total body weight for males\>50 kg (110 lbs). For females, total body weight \>45 kg (99 lbs).
- No evidence of active or latent or inadequately treated infection with Mycobacterium tuberculosis (TB)
Exclusion
- Evidence or history of any clinically significant illness, medical condition, or disease.
- Evidence or history of any clinically significant infections within the past 3 months.
- Use of tobacco- or nicotine-containing products in excess of the equivalent of 5 cigarettes per day.
Key Trial Info
Start Date :
September 1 2010
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 1 2010
Estimated Enrollment :
16 Patients enrolled
Trial Details
Trial ID
NCT01184001
Start Date
September 1 2010
End Date
September 1 2010
Last Update
October 13 2010
Active Locations (1)
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1
Pfizer Investigational Site
Singapore, Singapore, 188770