Overview
Study To Assess the Pharmacokinetics of AZD1656 During Coadministration With Simvastatin
Status:
Completed
Completed
Trial end date:
2010-08-01
2010-08-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
To assess the pharmacokinetics of AZD1656 during coadministration with Simvastatin.Phase:
Phase 1Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
AstraZenecaTreatments:
Simvastatin
Criteria
Inclusion Criteria:- Patients with a clinical diagnosis of T2DM for at least 1 year, treated with any
metformin or metformin with one other oral anti-diabetic drug (OAD)
- Body mass index between greater than or equal to 19 and less than or equal to 42 kg/m2
- HbA1c greater than 6.5% at enrollment
Exclusion Criteria:
- Clinically significant illness or clinically relevant trauma, as judged by the
Investigator, within 2 weeks before the first administration of the IP
- Significant cardiovascular event within the last 6 months prior to enrollment (eg,
myocardial infarction/acute coronary syndrome, revascularisation procedure, stroke or
transient ischaemic attack) or heart failure New York Heart Association (NYHA) class
III-IV