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A Randomized, Open, Single-Dose, Single-Centre, Cross-over, Phase I Study in Type 1 Diabetes Mellitus Patients to Estimate the Extent and Rate of Absorption of AZD1656 After Administration of a Tablet Formulation in the Fasting State and Just Before Food in Comparison With an Oral Suspension of AZD1
To evaluate the bioavailability of a tablet of AZD1656.
Age
20 - 65 years
Sex
ALL
Healthy Volunteers
No
Research site
San Antonio, Texas, United States
Start Date
December 1, 2008
Primary Completion Date
March 1, 2009
Completion Date
September 1, 2009
Last Updated
November 3, 2009
11
ACTUAL participants
AZD1656
DRUG
AZD1656
DRUG
Lead Sponsor
AstraZeneca
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT07455994