To Evaluate Safety and Tolerability After Multiple Oral Doses of AZD1656 in Type 2 Diabetes Patients on Top of Insulin
Launched by ASTRAZENECA · Oct 6, 2008
Trial Information
Current as of September 13, 2025
Completed
Keywords
ClinConnect Summary
No description provided
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Female with non child-bearing potential
- • Diagnosed Diabetes Mellitus patients treated with insulin alone or insulin in combination with other anti-diabetic drugs. Stable blood sugar control indicated by no changed treatment within 3 months prior to study start.
- • HbA1c below or equal to 11 % 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 of ischemic heart disease, stroke, transitorisk ischemic attack or symptomatic peripheral vascular disease
- • Clinically significant abnormalities in clinical chemistry, hematology, or urinalysis results.
About Astrazeneca
AstraZeneca is a global biopharmaceutical company dedicated to the discovery, development, and commercialization of innovative medicines across various therapeutic areas, including oncology, cardiovascular, respiratory, and autoimmune diseases. With a strong commitment to scientific research and patient-centric solutions, AstraZeneca leverages cutting-edge technology and a robust pipeline to address unmet medical needs. The company collaborates with healthcare professionals, academic institutions, and other organizations to advance clinical trials and deliver transformative therapies, aiming to improve health outcomes and enhance the quality of life for patients worldwide.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Chula Vista, California, United States
Patients applied
Trial Officials
Klas Malmberg, MD, PhD
Study Director
AstraZeneca R&D Mölndal
Marcus Hompesch, MD
Principal Investigator
Profil Institut for Clinical Research Inc.
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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