Healthy Volunteers, Pharmacologic Action
Conditions
Keywords
phase I, healthy volunteers, AZD3293, itraconazole, diltiazem, medazolam, drug interactions, Pharmacokinetics
Brief summary
This study is a single-center, open-label, 3-group, fixed-sequence drug-drug interaction study to assess the effect of coadministration of multiple-dose itraconazole or diltiazem on the single-dose PK of AZD3293 and the effects of coadministration of single- and multiple-dose AZD3293 on the single-dose PK of midazolam. The study will also evaluate the safety and tolerability of single and multiple oral doses of AZD3293, alone and in combination with itraconazole, diltiazem, and midazolam in healthy young subjects.AZD3293 is being developed for the treatment of Alzheimer's disease
Interventions
DRUGGroup 1 AZD3293
AZD3293 oral solution
DRUGGroup 2 AZD3293
AZD3293 oral solution
DRUGGroup 3 AZD3293
AZD3293 oral solution
DRUGGroup 1 Itraconazole
itraconazole capsule
DRUGGroup 2 Diltiazem
Diltiazem ER tablet
DRUGGroup 3 Midazolam
midazolam syrup
Sponsors
AstraZeneca
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
Yes
Inclusion criteria
* Provision of signed, written, and dated informed consent prior to any study-specific procedures Male and nonfertile female healthy subjects, aged 18 to 55 years at the time of consent * Body weight ≥50 to ≤100 kg and body mass index (BMI) ≥19 to ≤30 kg/m2 * Clinically normal findings on physical examination in relation to age, as judged by the Investigator * Male healthy subjects must be willing to use barrier contraception, ie, condoms, even if their partners are post-menopausal, surgically sterile, or using accepted contraceptive methods, from the first day of dosing until 3 months after the last dose of investigational product (IP)
Exclusion criteria
* Participation in any prior study of AZD3293 * History of any clinically significant disease or disorder which, in the opinion of the Investigator, may put the subject at risk because of participation in the study, may influence the results, or may limit the subject's ability to participate in the study * History or presence of gastrointestinal, hepatic or renal disease or any other condition known to interfere with absorption, distribution, metabolism or excretion of drugs * 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)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| The effect of multiple-dose co-administration of CYP3A4 inhibitors on the single-dose PK of AZD3293 measured by assessment of area under the curve over the time (AUC) and maximum concentration | up to day 13 | In Group 1, serial blood samples for AZD3293 plasma concentrations will be collected from predose to 96 hours after administration of AZD3293 on Day 1 and from predose to 144 hours after study drug administration on Day 8. Sparse blood samples for itraconazole plasma concentrations will be collected at predose (prior to administration of AZD3293) on Day 1 and 2 hours after the morning dose of itraconazole on Day 5 through Day 13. In Group 2, serial blood samples for AZD3293 plasma concentrations will be collected from predose to 96 hours after administration of AZD3293 on Day 1 and from predose to 144 hours after study drug administration on Day 8. Sparse blood samples for diltiazem plasma concentrations will be collected at predose (prior to administration of AZD3293) on Day 1 and 3 hours after diltiazem administration on Day 5 through Day 13. |
| The effect of multiple-dose AZD3293 administration (including the reversibilityof any of its effects) on the single-dose PK of a CYP3A4/CYP3A5 substrate (midazolam) by assessment of area under the curve over the time (AUC) and maximum concentration | up to day 17 | Serial blood samples for midazolam plasma concentrations will be collected from predose to 24 hours after administration of midazolam on Day 1 and Day 17 and for 48 hours after administration of midazolam on Day 8. Sparse blood samples for AZD3293 plasma concentrations will be collected at predose (prior to administration of midazolam) on Day 1 and 2 hours after AZD3293 administration on Day 2 through Day 10. |
Secondary
| Measure | Time frame |
|---|---|
| Safety and tolerability in terms of vital signs assessment (blood pressure, pulse and body temperature) and physical exams | from baseline and up till day 18 |
| Safety and tolerability by assessing changes in electrocardiogram (ECG) parameters | from Baseline and up to day 18 |
| Safety profile in terms of Adverse events assessment | from Baseline and up to day 18 |
| Suicidality mesured by Columbia-Suicide Severity Rating Scale (C-SSRS) | from Baseline and up till day 18 |
| Safety and tolerability by assessing telemetry records | from baseline and up to day 13 |
| Safety and tolerability in terms of lab tests assessment (hematology, chemistry, urinalysis) | from Baseline and up to day 18 |
Countries
United States
Outcome results
None listed