Expired Study
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Chula Vista, California


The purpose of this study is to investigate safety and tolerability after high Single Ascending Oral Doses of AZD1656.


Inclusion Criteria: - Provision of signed and dated, written informed consent prior to any study specific procedures. - Male, T2DM patients aged 20-60 years - Treatment with 1 to 2 OADs as Therapy for T2DM for at least 30 days prior to enrollment - Patients should not have been treated with glitazones within 6 months prior to enrollment - Male T2DM patients without known cardiovascular disease, with the exception of Grade 1 hypertension without secondary organ involvement (eg. grade 1 HT is allowed if no eye, kidney disease or LVH has been documented). Exclusion Criteria: - History of ischemic heart disease , heart failure, stroke, transitory ischemic attack or peripheral vascular disease. - Prolonged QTcF>450 msec or shortened QTcF<350 msec or family history of long QT syndrome. - Any clinically important abnormalities in rhythm, conduction or morphology of resting ECG that may interfere with the interpretation of QTc interval changes. - Systolic BP>159 mmHg or diastolic BP>99 mmHg at screening and on Day-1



Primary Contact:

Principal Investigator
Linda Morrow, MD
Profil Institute for Clinical Research, Inc.

Backup Contact:


Location Contact:

Chula Vista, California
United States

There is no listed contact information for this specific location.

Site Status: N/A

Data Source: ClinicalTrials.gov

Date Processed: August 31, 2019

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