The purpose of this study is to assess the pharmacokinetics of AZD6140 and its active
metabolite, safety, tolerability of AZD6140 following single administration in healthy male
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Full eligibility criteria for NCT01588626
Ages eligible for Study
20 Years to 45 Years
Genders eligible for Study
Accepts Healthy Volunteers
Healthy male subject aged between 20 to 45 years inclusive
Body mass index (BMI=weight/height2) between 18.0 to 27.0 kg/m2 inclusive
Body weight between 50.0 to 85.0 kg inclusive Provision of written informed consent
Clinically significant abnormalities in clinical chemistry, haematology or urinalysis results as judged by the investigator, or positive results on screening tests for serum hepatitis B surface antigen and hepatitis C antibody, syphilis and human immu
Supine blood pressure > 150 mmHg systolic or > 95 mmHg diastolic or supine pulse > 90 beats per minute (after resting for 10 minutes) Personal or family history of bleeding disorders, or reasonable suspicion of vascular malformations, including aneurysms
Personal or familial predisposition for thrombotic disorders Clinically significant medical history, including psychiatric disorders and severe allergies
All locations for NCT01588626
View full eligibility
Tris trial is registered with FDA with number: NCT01588626. The sponsor of the trial is AstraZeneca and it is looking for 12 volunteers for the current phase.
Official trial title: A Phase I, Single Centre, Open Study to Assess the Pharmacokinetics of Oral AZD6140 After Single Dose in Healthy Japanese Male Volunteers
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