Relative Bioavailability Study to Assess Two Solid Formulations Compared to an Oral Solution of AZD3293 in Healthy Male and Non-Fertile Female Subjects

Phase 1

Completed

• Conditions: Healthy Volunteers; Pharmacologic Action
• Interventions: Drug: AZD3293 oral solution; Drug: AZD3293 tablet formulation A; Drug: AZD3293 tablet formulation B

• Registration Number: NCT02039180
• Lead Sponsor: AstraZeneca

Brief Summary

This is an open-label, randomized, 3-period crossover, single dose study. Three (3) single doses of AZD3293 (2 different tablet formulations, and an oral solution) will be administered with a washout period of at least 1 week between the doses to investigate the relative bioavailability of AZD3293 after administration via 2 tablet formulations compared with oral solution and to evaluate basic systemic pharmacokinetic parameters of the tablet formulations compared to the oral solution of AZD3293.

The safety and tolerability of AZD3293 in healthy subjects will also be assessed in the study. AZD3293 is being developed for the treatment of Alzheimer's disease

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2014-01-16
• Study First Submitted QC: 2014-01-16
• Study First Posted: 2014-01-17
• Study Start: 2014-02
• Primary Completion: 2014-03
• Study Completion: 2014-03
• Status Verified: 2014-04
• Last Update Submitted: 2014-04-23
• Last Update Posted: 2014-04-24

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 1

Inclusion Criteria

1. Provision of signed, written, and dated informed consent prior to any study-specific procedures
2. Healthy subjects must be able to understand and be willing to comply with study procedures, restrictions, and requirements.
3. Male and non-fertile female healthy subjects, aged 18 to 55 years
4. Body weight ≥50 to ≤100 kg and body mass index (BMI) ≥19 to ≤30 kg/m2
5. Clinically normal findings on physical examination in relation to age, as judged by the Investigator

Exclusion Criteria

1. History of 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 results or the subject's ability to participate in the study
2. History or presence of gastrointestinal, hepatic or renal disease or any other condition known to interfere with absorption, distribution, metabolism or excretion of drugs
3. History of previous or ongoing psychiatric disease/condition including psychosis, affective disorder, anxiety disorder, borderline state and personality disorder according to the criteria in the Diagnostic and Statistical Manual of Mental Disorders, 4th edition (DSM IV), as assessed by the Mini-International Neuropsychiatric Interview (MINI)

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Arm && Interventions

Group	Intervention	Description
AZD3293 oral solution	AZD3293 oral solution	single doses in random order in 3 study periods for each subject (Day 1 or Day 8 or Day 15)
AZD3293 tablet formulation A	AZD3293 tablet formulation A	single doses in random order in 3 study periods for each subject (Day 1 or Day 8 or Day 15)
AZD3293 tablet formulation B	AZD3293 tablet formulation B	single doses in random order in 3 study periods for each subject (Day 1 or Day 8 or Day 15)

Primary Outcome Measures

Name	Time	Method
The relative bioavailability of AZD3293 after administration via 2 tablet formulations compared with oral solution by assessment of the area under the plasma concentration-time curve from zero to infinity for the tablet formulations and the oral solutio	up to day 18 (Day 1 - 72 hrs post-dose on Day 15)	Blood samples for determination of plasma concentrations of AZD3293 and its active metabolite will be collected at pre-dose (15 or 30 min) and 30 min, 1h, 1.5, 2, 3, 4, 6, 8, 12, 24, 36, 48, 56 and 72 hours post-dose starting on Days 1, 8 \& 15 and analyzed according to fully validated methods.
To compare the tablet formulations of AZD3293 with the oral solution of AZD3293 by evaluation of the basic pharmacokinetic parameters for each formulation	up to day 18 (Day 1 - 72 hrs post-dose on Day 15)	Blood samples for determination of plasma concentrations of AZD3293 and its active metabolite will be collected at pre-dose (15 or 30 min) and 30 min, 1h, 1.5, 2, 3, 4, 6, 8, 12, 24, 36, 48, 56 and 72 hours post-dose starting on Days 1, 8 \& 15 and analyzed according to fully validated methods.

Secondary Outcome Measures

Name	Time	Method
Safety profile in terms of Adverse events assessment	From Baseline and up to day 25
Safety and tolerability in terms of lab tests assessment (hematology, chemistry, urinalysis)	From Baseline and up to day 25
Safety and tolerability in terms of vital signs assessment (blood pressure, pulse and body temperature) and physical exams	From baseline and up to day 25
Safety and tolerability by assessing changes in electrocardiogram (ECG) parameters	from baseline and up until day 25

Trial Locations

Locations (1)

Research Site; 🇺🇸 Cypress, California, United States