Overview
Study to Assess Effect of Cyclosporine on the Blood Levels of Ticagrelor
Status:
Completed
Completed
Trial end date:
2012-06-01
2012-06-01
Target enrollment:
0
0
Participant gender:
Male
Male
Summary
The purpose of this study is to assess the effect of Cyclosporine on the blood levels of Ticagrelor.Phase:
Phase 1Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
AstraZenecaTreatments:
Cyclosporine
Cyclosporins
Ticagrelor
Criteria
Inclusion Criteria:- Provision of signed and dated written informed consent prior to any study-specific
procedures
- Healthy male subjects aged 18 to 45 years (inclusive) with suitable veins for
cannulation or repeated venipuncture
Exclusion Criteria:
- History or presence of gastrointestinal, hepatic or renal disease, or any other
condition known to interfere with absorption, distribution, metabolism, or excretion
of drugs
- A history of hemophilia, von Willebrand's disease, lupus anti-coagulant, or other
diseases/syndromes that can either alter or increase the propensity for bleeding
- A personal history of vascular abnormalities including aneurysms; a personal history
of severe hemorrhage, hematemesis, melena, hemoptysis, severe epistaxis, severe
thrombocytopenia, intracranial hemorrhage, or rectal bleeding within 1 year