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A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Examine Safety and Pharmacokinetics of Exenatide Long-Acting Release Administered Weekly in Subjects With Type 2 Diabetes Mellitus
Exenatide LAR is a long-acting release formulation of exenatide, which is a twice-daily dosage form currently under investigation as a potential treatment for people with type 2 diabetes mellitus. This study will assess the safety, tolerability, and pharmacokinetics of Exenatide LAR administered weekly by subcutaneous injection in people with type 2 diabetes mellitus.
Age
18 - 75 years
Sex
ALL
Healthy Volunteers
No
Research Site
Walnut Creek, California, United States
Research Site
Honolulu, Hawaii, United States
Research Site
St Louis, Missouri, United States
Research Site
Butte, Montana, United States
Research Site
Portland, Oregon, United States
Research Site
San Antonio, Texas, United States
Research Site
Olympia, Washington, United States
Start Date
February 1, 2005
Primary Completion Date
October 1, 2005
Completion Date
October 1, 2005
Last Updated
February 24, 2015
45
ACTUAL participants
placebo
DRUG
placebo
DRUG
Exenatide LAR
DRUG
Exenatide LAR
DRUG
Lead Sponsor
AstraZeneca
Collaborators
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 ConditionsNCT07433062