Status:
COMPLETED
Study Evaluating Single Doses of ILV-095 in Healthy Subjects
Lead Sponsor:
Wyeth is now a wholly owned subsidiary of Pfizer
Conditions:
Healthy Subjects
Eligibility:
All Genders
18-50 years
Phase:
PHASE1
Brief Summary
The purpose of this study is to evaluate the safety and tolerability of single doses of ILV-095 in healthy subjects.
Eligibility Criteria
Inclusion
- Healthy men and women of non-childbearing potential ages 18 to 50 years old.
- Body mass index (BMI) in the range of 18 to 32 kg/m2 and body weight greater than or equal to50 kg.
- Healthy as determined by the investigator on the basis of screening evaluations.
- Nonsmoker or smoker of fewer than 10 cigarettes per day as determined by history. Must be able to abstain from smoking during the inpatient stay.
- Have a high probability for compliance with and completion of the study.
Exclusion
- Presence or history of any disorder that may prevent the successful completion of the study.
- Any subject who had orthopedic surgery within 12 weeks of the screening visit or has planned (elective) orthopedic surgery within 12 weeks of study drug administration.
- Acute disease state (eg, nausea, vomiting, fever, active infection, or diarrhea) within 7 days before enrollment.
Key Trial Info
Start Date :
January 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
August 1 2009
Estimated Enrollment :
48 Patients enrolled
Trial Details
Trial ID
NCT00822835
Start Date
January 1 2009
End Date
August 1 2009
Last Update
September 18 2009
Active Locations (1)
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1
Philadelphia, Pennsylvania, United States, 19148