Study to Evaluate the Interaction Between Aspirin and Nexium
Completed · Phase 1
Conditions studied: Healthy Volunteers
In brief
The purpose of this study is to assess the interaction between aspirin and Nexium in healthy volunteers.
Key facts
- Study ID
- NCT01199328
- Run by
- AstraZeneca
- People needed
- 34
- Starts
- 2010-09-01
- Expected to finish
- 2010-11-01
- Last updated by the study team
- 2010-11-19
Who can join
Age: 18 and older, up to 75. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Provision informed consent prior to any study specific procedures.
- Healthy male and female subjects aged 18 to 75 years with suitable veins for cannulation or repeated vein puncture.
- Healthy female subjects must be of non-childbearing potential (post-menopausal, had a hysterectomy and/or bilateral oophorectomy) or be of childbearing potential and have a negative serum hCG pregnancy test during screening and be using of the following methods of birth control:
- Continuously practice abstinence during screening and throughout the duration of the study
- Clinically accepted contraception as described under item 7 of Section 5.1 and on hormonal contraceptives.
- Have a body mass index (BMI) between 19 and 30 kg/m2
- No clinically significant abnormal findings as judged by the Investigator on enrollment physical exam.
You may not qualify if…
- Involvement in the planning and/or conduct of the study (applies to both AstraZeneca staff and/or staff at the study site)
- Previous enrolment or randomisation in the present study.
- History of any clinically significant disease or disorder which, in the opinion of the investigator, may either put the subject at risk because of participation in the study, or influence the results or the subject's ability to participate in the study e.g. history of any bleeding disorder, excessive bruising or ongoing or history of liver disease
- History or presence of clinically significant gastrointestinal e.e. GI ulcer, hepatic or renal disease or any other condition known to interfere with absorption, distribution, metabolism or excretion of drugs.
- Any clinically significant illness within 4 weeks of the first administration of investigational product.
Where it is running
- Research Site — Springfield, Missouri, United States
Full record on ClinicalTrials.gov
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