Skip to content

AZD8529 Multiple Ascending Dose Study in Healthy Subjects

A Phase I, Single-Center, Randomized, Double-Blind, Placebo-Controlled, Study to Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of AZD8529 When Given as Single and Multiple Ascending Oral Doses in Healthy Subjects

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00765492
Enrollment
47
Registered
2008-10-03
Start date
2008-10-31
Completion date
2009-03-31
Last updated
2009-06-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy Volunteer

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

DRUGPlacebo

oral

Sponsors

AstraZeneca
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 45 Years
Healthy volunteers
Yes

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

MeasureTime 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

MeasureTime frame
To characterize the pharmacokinetics of AZD8529 in plasmaBlood samples will be taken during the study.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026