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Phase 3 N=380 Treatment

Study to Evaluate the Long-Term Safety of PA32540 in Subjects Who Are at Risk for Developing Aspirin-Associated Gastric Ulcers

Aspirin-Associated Gastric Ulcers

Enrolled (actual)
380
Serious AEs
14.5%
Results posted
Feb 2016
Primary outcome: Primary: Number of Subjects Monitored for Long-term Safety of PA32540 — 379 participants

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
PA32540 (Drug)
Age
Adult, Older Adult · 55+ yrs
Sex
All
Sponsor
POZEN
Primary completion
May 2011

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Subjects Monitored for Long-term Safety of PA32540
379
SECONDARY
Most Frequent Treatment Emergent Adverse Events Leading to Study Drug Discontinuation
51; 15; 7; 6; 6

Summary

This study uses an open-label design and will be conducted in approximately 40 sites in the United States. Approximately 400 subjects will be enrolled in the study to ensure that approximately 300 subjects will have 6 months exposure to PA32540 and at least 100 subjects will have 12 months exposure to PA32540.

Eligibility Criteria

Inclusion criteria

  • A. Male or non-pregnant, non-breastfeeding females who have been on daily aspirin 325 mg for at least three months and who are expected to use daily aspirin 325 mg for at least six months (Daily is defined as "at least 5 days per week"):

AND, who are

  • 55 years of age and older; or
  • 18 - 54 years of age and have a history of a documented gastric or duodenal ulcer within the past five years.
  • A. Aspirin use should be for the secondary prevention of cardiovascular or cerebrovascular events as defined as follows:

Have been diagnosed with or have had a history of

  • MI (myocardial infarction that has been confirmed or suspected)
  • Ischemic stroke
  • TIA (transient ischemic attack)

Or have established, clinically significant coronary and other atherosclerotic vascular disease (meaning at high risk for surgical intervention or for MI, TIA, stroke, if left untreated), including:

  • Angina (stable or unstable)
  • Peripheral arterial disease
  • Atherosclerotic aortic disease
  • Carotid artery disease Or have had
  • CABG (coronary artery bypass graft)
  • PCI (percutaneous coronary intervention with or without stent)
  • Carotid endarterectomy
  • A. If female, subjects are eligible if they are of
  • non-childbearing potential (i.e., physiologically incapable of becoming pregnant); or,
  • childbearing potential, have a negative pregnancy test at screening, and at least one of the following applies or is agreed to by the subject:
  • Female sterilization or sterilization of male partner
  • Hormonal contraception by oral route, implant, injectable, vaginal ring
  • 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)
  • Any other method with published data showing that the lowest expected failure rate is less than 1% per year 4. Able to understand and comply with study procedures required and able and willing to provide written informed consent prior to any study procedures being performed

Exclusion criteria

  • Any current gastric, esophageal or duodenal ulcer
  • Positive test result for H. pylori at screening 3A. Have had a revascularization procedure (i.e., Coronary Artery Bypass Graft, Percutaneous Transluminal Coronary Angioplasty, or carotid endarterectomy) less than six months prior to screening
  • Unstable hypertension as judged by the Investigator 5. Uncontrolled diabetes mellitus as judged by the Investigator 6. Unstable cardio- or cerebrovascular disease such that it would endanger the subject if they participated in the trial 7. Clinically significant valvular disease 8. Congestive heart failure or other cardiovascular symptoms according to New York Heart Association (NYHA) Functional Classification III-IV (Appendix 3) 9. History of hypersensitivity to omeprazole or to another proton pump inhibitor 10. History of allergic reaction or intolerance to aspirin and/or a history of aspirin-induced symptoms of asthma, rhinitis, and/or nasal polyps 11. History of serious UGI event, such as bleeding, perforation, or obstruction 12. Gastrointestinal disorder or surgery leading to impaired drug absorption 13. Presence of chronic or uncontrolled acute medical illness, e.g. gastrointestinal disorder (esophageal stricture, severe esophagitis, long-segment Barrett's esophagus, signs and symptoms of gastric outlet obstruction), thyroid disorder and/or infection that would endanger a subject if they were to participate in the study 14. Schizophrenia, uncontrolled bipolar disorder, or severe depression 15. History of alcoholism or drug addiction within a year prior to enrollment in the study 16. Severe hepatic dysfunction (i.e. cirrhosis or portal hypertension) 17. Blood coagulation disorder, including use of systemic anticoagulants such as warfarin or other vitamin K antagonists 18. Any condition that, in the opinion of the Investigator, may either put the subject at risk or in
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00995410). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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