Healthy
Conditions
Keywords
Gastroprotective effects, Aspirin
Brief summary
To compare the gastroprotective effects of a once-daily dose of PA 325 combination tablet
Detailed description
Primary: To compare the gastroprotective effects of a once-daily dose of PA 325 combination tablet combining 325 mg pH sensitive aspirin and 20 mg immediate release omeprazole versus a once-daily dose of 81 mg enteric coated (EC) aspirin utilizing Lanza scores from endoscopy findings in normal healthy volunteers. Secondary: To evaluate the safety and gastrointestinal tolerability, including ulcerogenic potential, and the effect on gastric pH of PA 325.
Interventions
DRUGaspirin
DRUGomeprazole
Sponsors
POZEN
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
1. Subject is a male or a female who is not pregnant or is not lactating. A female is eligible to enter and participate in this study if she is of: * Non-childbearing potential (i.e., physiologically incapable of becoming pregnant); or, * Childbearing potential has a negative pregnancy test at screening, and at least one of the following applies or is agreed to by the subject: * Complete abstinence from intercourse for at least 14 days prior to first dose of study medication, throughout the study and for 30 days after completion of the study * Female sterilization or sterilization of male partner; or, * Hormonal contraception by oral route, implant, injectable, vaginal ring; or, * Any intrauterine device (IUD) with published data showing that the lowest expected failure rate is less than 1% per year; * Double barrier method (2 physical barriers or 1 physical barrier plus spermicide); or * Any other method with published data showing that the lowest expected failure rate is less than 1% per year 2. Subject is \> 50 years of age inclusive at the time of dosing 3. Subject does not currently smoke and has not smoked for at least 3 months 4. The subject's physical status is within normal limits of age and consistent with observations at screening 5. The subject's Body Mass Index (BMI) is between 20-30 kg/m2 6. Each subject must be able to understand and comply with study procedures required of a subject and is able and willing to provide written informed consent prior to any study procedures being performed
Exclusion criteria
1. History of hypersensitivity to omeprazole or to another proton-pump inhibitor 2. History of allergic reaction or intolerance to aspirin or any NSAID and/or a history of NSAID-induced symptoms of asthma, rhinitis, and/or nasal polyps 3. Participation in any study of an investigational treatment in the 4 weeks before Day 1 dosing 4. Presence of uncontrolled acute or chronic medical illness, e.g. GI disorder, hypertension, diabetes, thyroid disorder, depression and/or infection that would endanger a subject if they were to participate in the study 5. GI disorder or surgery leading to impaired drug absorption 6. Evidence of uncontrolled, or unstable cardio- or cerebrovascular disorder, which in the investigator's opinion, would endanger a subject if he or she were to participate in the study 7. Schizophrenia or bipolar disorder 8. Use of any concomitant medication not approved by the study physician during the washout period and during the study conduct 9. Serious blood coagulation disorder, including use of systemic anticoagulants 10. Subjects who donated 50 to 499 mL of blood within 30 days and more than 499 mL within 56 days prior to dosing 11. Subjects who, through completion of the study, would have donated in excess of: 500 mL of blood in 14 days; 1,500 mL of blood in 180 days; 2,500 mL of blood in 1 year 12. Baseline endoscopy showing any gastric or duodenal mucosal abnormality (hemorrhages, ulcers or erosions) 13. Gastric pH \> 3 at Day - 1 endoscopy 14. Screening laboratory alanine transaminase (ALT) or aspartate transaminase (AST) value \> 2 times the upper limit of normal 15. Estimated creatinine clearance \< 30 ml/min at screening 16. Other than noted specifically, any screening laboratory value that is clinically significant in the investigator's opinion and would endanger a subject if he or she were to participate in the study 17. History of hepatitis B or C, a positive test for hepatitis B surface antigen, hepatitis C antibody, a history of HIV infections, or demonstration of HIV antibodies 18. History of malignancy, treated or untreated, within the past 5 years, with the exception of successfully treated basal cell or squamous cell carcinoma of the skin 19. Subjects who have previously been a screen failure in this study 20. Subject has excessive alcohol use (\>2 units per day on average; for example 2 bottles of beer, two glasses of wine, 2 ounces of liquor/spirits), or recent history (in the past 3 months) suggestive of alcohol or drug abuse or dependence 21. Subject has ingested grapefruit or grapefruit juice within 10 days of dosing or will ingest grapefruit or grapefruit juice during the duration of the study 22. Positive illicit drug screen
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint is the occurrence of gastric and/or duodenal bulb lesions meeting Grade 3 or Grade 4 Lanza (1988) scores for the stomach and duodenal bulb (combined). | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoints include the incidence of gastric and/or duodenal ulcers, total number of gastric and/or duodenal erosions, gastric pH and any other GI tolerability issues. | — |
Countries
Canada, United States
Outcome results
None listed