A First Time in Man, Study to Assess the Safety of AZD8329 After Single Ascending Oral Doses
- Registration Number
- NCT00935662
- Lead Sponsor
- AstraZeneca
- Brief Summary
The primary objective for this study is to assess the safety and tolerability of AZD8329 when given as a single dose in increasing dose strength, and also to identify the highest tolerated dose for future studies.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Male
- Target Recruitment
- 119
Inclusion Criteria
- Provision of informed consent prior to any study specific procedures
- Have a body mass index between 19 and 30 kg/m2 and weigh at least 50 kg
Exclusion Criteria
- Any clinically significant disease or disorder which, in the opinion of the investigator, may either put the subject at risk because of participation in the study, or influence the result of the study, or the subject´s ability to participate
- Any clinically significant abnormalities in clinical chemistry, haematology or urinalysis results as judged by the investigator
- Any clinically important abnormalities in rhythm, conduction or morphology of resting ECG that may interfere with the interpretation of QTc interval changes.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description AZD8329 AZD8329 AZD8329 oral solution Placebo Placebo Placebo for AZD8329 oral solution
- Primary Outcome Measures
Name Time Method Safety measurements (ECG's, Pulse, Blood Pressure, Safety Laboratory and Adverse Events) Safety will be monitored continously and safety assessments will be made on several occasions throughout the whole study.
- Secondary Outcome Measures
Name Time Method PK samples for AZD8329 Intense PK-sampling during the 24 hours following administration of investigational product and additional samples up to 72 hours after dose.
Trial Locations
- Locations (1)
Research Site
🇸🇪Uppsala, Sweden