Study to Evaluate Methods That Assess the Effect of AZD4017 in Adipose Tissue
- Registration Number
- NCT01096004
- Lead Sponsor
- AstraZeneca
- Brief Summary
The primary purpose of this study is to investigate different methods to evaluate the effect of AZD4017 in adipose tissue after single and multiple doses of AZD4017 in abdominally obese but otherwise healthy subjects.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Male
- Target Recruitment
- 15
Inclusion Criteria
- Provision of signed written and dated informed consent
- Have a body mass index (BMI) between 27 and 35 kg/m2
- Waist circumference of >102 cm
Exclusion Criteria
- History of any clinical significant disease
- Any clinically significant illness, medical/surgical procedure or trauma within 4 weeks of the first administration of investigational product
- Any clinically significant abnormalities in clinical chemistry, haematology or urinalysis results as judged by the investigator
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description 1 AZD4017 - 2 Placebo -
- Primary Outcome Measures
Name Time Method To investigate the effect of single and repeated doses of AZD4017 and placebo on mechanisms in adipose tissue involved in metabolic regulation A adipose tissue biospy is taken at baseline, on first day of dosing day, on 4th dosing day and on 9th dosing day.
- Secondary Outcome Measures
Name Time Method Safety and Tolerability (Adverse events, vital signs, ECGs, physical examination, laboratory variables The variables will be measure predose and the repeatedly during the following 10 days after dosing
Trial Locations
- Locations (1)
Research Site
πΈπͺGoteborg, Sweden