Expired Study
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Chula Vista, California


Purpose:

The purpose of this study is to assess safety and tolerability of AZD1656 after multiple repeated oral doses in patients with type 2 diabetes


Criteria:

Inclusion Criteria: - Male or surgically sterile female of non-childbearing potential (post-menopausal, ie natural or induced menopause with last menstruation >1 year ago and LH and FSH in the post-menopausal range, and/or have undergone hysterectomy and/or bilateral oophorectomy - Diagnosed diabetes Mellitus patients treated with diet and exercise alone or with up to two oral anti-diabetic drugs. Stable glycemic control indicated by no changed treatment within 3 months prior to enrollment - HbA1c ≤10.5 % at screening (HbA1c value according to international DCCT standard) Exclusion Criteria: - Clinically significant illness or clinically relevant trauma, as judged by the investigator, within two weeks before the first administration of the IP - History ischemic heart disease, stroke, transitorisk ischemic attack or symptomatic peripheral vascular disease - Clinically significant abnormalities in clinical chemistry, hematology, or urinalysis results. Positive test of Hepatitis B surface antigen, antibodies to HIV virus and antibodies to Hepatitis C virus


NCT ID:

NCT00747175


Primary Contact:

Study Director
Klas Malmberg, MD, Phd, Prof
AstraZeneca R&D Mölndal, SE-431 83 Mölndal, Sweden


Backup Contact:

N/A


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: October 09, 2019

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