Healthy Volunteer
Conditions
Keywords
Phase I
Brief summary
This is a study to evaluate safety, tolerability, PK and PD effects of orally administered AZD8529 after multiple ascending doses
Interventions
oral
oral
Sponsors
Study design
Eligibility
Inclusion criteria
* Female subjects must be of non-child bearing potential.
Exclusion criteria
* Has received another new chemical entity (defined as a compound which has not been approved for marketing) or has participated in any other clinical study that included drug treatment within 30months of the first administration of investigational prod * Plasma donation within one month of screening or any blood donation/blood loss \> 500mL during the 3 months prior to screening * Clinically relevant abnormalities in physical examinations, vital signs, ECG, clinical chemistry, hematology or urinalysis
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To assess the safety and tolerability of multiple dose administration of AZD8529 when given orally to healthy male subjects and female subjects of non-childbearing potential. | each visit, at least daily, during the study. |
Secondary
| Measure | Time frame |
|---|---|
| To characterize the pharmacokinetics of AZD8529 in plasma | Blood samples will be taken during the study. |