A Study of Aleglitazar in Combination With Aspirin in Healthy Volunteers
Status: | Completed |
---|---|
Conditions: | Healthy Studies |
Therapuetic Areas: | Other |
Healthy: | No |
Age Range: | 40 - 65 |
Updated: | 8/3/2016 |
Start Date: | July 2010 |
End Date: | October 2010 |
A Randomized, Double-blind, Placebo-controlled, Parallel Group Study to Investigate the Effect of 150 µg Aleglitazar Once Daily in Healthy Subjects Treated With 325 mg Aspirin Once Daily on Renal Function, Renin-angiotensin System and Platelet Aggregation
This randomized, double-blind, placebo-controlled, parallel group study will investigate the
safety and tolerability, and the effect of aleglitazar in combination with aspirin on renal
function, renin-angiotensin system and platelet aggregation in healthy volunteers.
Volunteers will be randomized to receive daily doses of aleglitazar or placebo in
combination with aspirin. The anticipated time on study drug is 5 weeks.
safety and tolerability, and the effect of aleglitazar in combination with aspirin on renal
function, renin-angiotensin system and platelet aggregation in healthy volunteers.
Volunteers will be randomized to receive daily doses of aleglitazar or placebo in
combination with aspirin. The anticipated time on study drug is 5 weeks.
Inclusion Criteria:
- Healthy volunteers, aged 40 to 65 years inclusive
- Body Mass Index (BMI) between 18 and 35 kg/m2 inclusive
- Females of child-bearing potential must be willing to use two acceptable methods of
contraception during the study and at least 3 months before start of the study
- Non-smoker or currently smoking less than 5 cigarettes (or equivalent amount of other
tobacco products) per day and is willing and able to stop smoking during the period
in study center
- Volunteer drinks no more than 3 cups of coffee, tea or soft drinks per day and is
willing and able to stop drinking coffee, tea and soft drinks during the period in
study center
Exclusion Criteria:
- Any clinically relevant abnormal laboratory test results at screening
- Volunteer has taken any prescribed, herbal or over-the-counter medication within 2
weeks prior to first dosing
- A history of any clinical significant gastro-intestinal, cardiovascular,
musculoskeletal, endocrine, hematological, psychiatric, renal, hepatic,
bronchopulmonary or neurological conditions or lipid disorders
- A positive test for human immunodeficiency virus (HIV-1 or HIV-2), hepatitis B or
hepatitis C
- History of intolerance to non-steroidal anti-inflammatory drugs (NSAIDs) or aspirin,
history of gastric or duodenal ulceration, personal or family history of abnormal
clotting or bleeding
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