Healthy Participants
Conditions
Keywords
Serine/protein kinase AKT, Anti-cancer agent, Pharmacokinetics, Protein kinase
Brief summary
The purpose of this study is to assess the effect of capivasertib on the pharmacokinetics of oral dextromethorphan in healthy participants.
Detailed description
This is an open-label, fixed sequence study conducted at a single study centre. The study will comprise of: * A Screening Period (from Day -28 to Day -2) * In-house treatment period (from Day -1 to Day 8) Period 1 (from Day -1 to Day 3): Participants will receive single oral doses of dextromethorphan during this period. Period 2 (from Day 4 to Day 8): Participants will receive 2 doses of capivasertib and a single dose of dextromethorphan during this period. • Follow-up Visit within 7 to 10 days after the last administration of the Investigative Medical Products (from Day 13 to Day 16).
Interventions
DRUGDextromethorphan
Dextromethorphan will be administered orally once in Period 1 and once in Period 2
DRUGCapivasertib
Capivasertib will be administered orally twice in Period 2
Sponsors
AstraZeneca
Parexel
Study design
Allocation
NA
Intervention model
SEQUENTIAL
Primary purpose
OTHER
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes
Inclusion criteria
Main Inclusion Criteria: * Have a Body Mass Index (BMI) between 18 and 30 kg/m2 inclusive and weigh at least 50 kg. * All females must have a negative pregnancy test at the Screening Visit and on admission to the Clinical Unit. * Females of non-childbearing potential must be confirmed at the screening visit (postmenopausal or documentation of irreversible surgical sterilisation). * Male participants must have documentation of vasectomy done 6 months prior to screening visit. Participants must be willing to use one barrier method of contraception (condom) during sexual intercourse with a female partner of childbearing potential from the time of first study intervention administration until 16 weeks after the last dose of capivasertib. Main
Exclusion criteria
* History of any clinically important disease or disorder * History or presence of gastrointestinal, hepatic or renal disease. * Any clinically important illness, medical/surgical procedure (excluding placement of vascular access), or significant traumatic injury within 4 weeks of the first administration of study intervention or an anticipated need for major surgery during the study. * Any clinically significant skin abnormalities that are chronic or currently active. * Abnormal hepato-renal and bone marrow organ function laboratory values. * Any clinically important abnormalities in clinical chemistry, haematology, or urinalysis. * Any clinically significant abnormalities in glucose metabolism. * Any positive result on screening for serum HBsAg OR anti-HBc antibody, indicative of active hepatitis B, hepatitis C, or human immunodeficiency virus (HIV) * Current smokers or those who have smoked or used other nicotine/nicotine-containing products within the previous 3 months prior to Screening Visit. * Known or suspected history of alcohol or drug abuse or excessive intake of alcohol. * Use of drugs with enzyme inducing properties 3 weeks prior to the first administration of study intervention. * Use of strong inhibitors of Cytochrome P450 3A4 (CYP3A4) or strong/moderate inducers of CYP3A4 within 2 weeks prior to first dose of capivasertib. * Concurrent use of herbal or natural products intended as treatment or prophylaxis that may interact with capivasertib. * Participants who have previously received capivasertib. * Any clinically significant abnormal findings in vital signs and 12-lead electrocardiogram (ECG). * History of severe allergy/hypersensitivity
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Area under concentration time curve from time 0 to infinity (AUCinf) of dextromethorphan | Period 1: Day 1 to Day 3, Period 2: Day 6 to Day 8 | To evaluate the PK (AUCinf) of dextromethorphan when administered orally alone and following oral dosing of capivasertib |
| Area under concentration curve from time 0 to the last quantifiable concentration (AUClast) of dextromethorphan | Period 1: Day 1 to Day 3, Period 2: Day 6 to Day 8 | To evaluate the PK (AUClast) of dextromethorphan when administered orally alone and following oral dosing of capivasertib |
| Maximum observed drug concentration (Cmax) of dextromethorphan | Period 1: Day 1 to Day 3, Period 2: Day 6 to Day 8 | To evaluate the PK (Cmax) of dextromethorphan when administered orally alone and following oral dosing of capivasertib |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Area under concentration curve from time 0 to the last quantifiable concentration (AUClast) of capivasertib | Period 2: Day 5 to Day 8 | To evaluate the PK (AUClast) of capivasertib following oral dosing |
| Time to reach maximum observed concentration (tmax) of capivasertib | Period 2: Day 5 to Day 8 | To evaluate the PK (tmax) of capivasertib following oral dosing |
| Maximum observed drug concentration (Cmax) of capivasertib | Period 2: Day 5 to Day 8 | To evaluate the PK (Cmax) of capivasertib following oral dosing |
| Ratio of AUCinf following co-administration to AUCinf following dosing alone (R AUCinf) of dextromethorphan | Period 1: Day 1 to Day 3, Period 2: Day 6 to Day 8 | To evaluate the PK (R AUCinf) of dextromethorphan following oral dosing |
| Ratio of AUClast following co-administration to AUClast following dosing alone (R AUClast) of dextromethorphan | Period 1: Day 1 to Day 3, Period 2: Day 6 to Day 8 | To evaluate the PK (R AUClast) of dextromethorphan following oral dosing |
| Ratio of Cmax following co-administration to Cmax following dosing alone (R Cmax) of dextromethorphan | Period 1: Day 1 to Day 3, Period 2: Day 6 to Day 8 | To evaluate the PK (R Cmax) of dextromethorphan following oral dosing |
| Terminal elimination half-life (t1/2λz) of dextromethorphan | Period 1: Day 1 to Day 3 | To evaluate the PK (t1/2λz) of dextromethorphan following oral dosing |
| Terminal rate constant (λz) of dextromethorphan | Period 1: Day 1 to Day 3 | To evaluate the PK (λz) of dextromethorphan following oral dosing |
| Time to reach maximum observed concentration (tmax) of dextromethorphan | Period 1: Day 1 to Day 3 | To evaluate the PK (tmax) of dextromethorphan following oral dosing |
| Area under concentration time curve from time 0 to infinity (AUCinf) of metabolite (dextrorphan) | Period 1: Day 1 to Day 3 | To evaluate the PK (AUCinf) of dextromethorphan following oral dosing |
| Area under concentration curve from time 0 to the last quantifiable concentration (AUClast) of metabolite (dextrorphan) | Period 1: Day 1 to Day 3 | To evaluate the PK (AUClast) of dextromethorphan following oral dosing |
| Maximum observed drug concentration (Cmax) of metabolite (dextrorphan) | Period 1: Day 1 to Day 3 | To evaluate the PK (Cmax) of dextromethorphan following oral dosing |
| Ratio of AUClast following co-administration to AUClast following dosing alone (R AUClast) of metabolite (dextrorphan) | Period 1: Day 1 to Day 3, Period 2: Day 6 to Day 8 | To evaluate the PK (R AUClast) of dextromethorphan following oral dosing |
| Terminal elimination half-life (t1/2λz) of metabolite (dextrorphan) | Period 1: Day 1 to Day 3 | To evaluate the PK (t1/2λz) of dextromethorphan following oral dosing |
| Terminal rate constant (λz) of metabolite (dextrorphan) | Period 1: Day 1 to Day 3 | To evaluate the PK (λz) of dextromethorphan following oral dosing |
| Time to reach maximum observed concentration (tmax) of metabolite (dextrorphan) | Period 1: Day 1 to Day 3 | To evaluate the PK (tmax) of dextromethorphan following oral dosing |
| Number of participants with adverse events (AEs) and serious AEs | Up to Day 16 | To examine the safety and tolerability of capivasertib when administered with dextromethorphan |
| Percentage change from baseline in bilirubin levels | Period 1: Day 1 to Day 2, Period 2: Day 4 to Day 7 | To evaluate the effect of capivasertib dosing on total, conjugated, and unconjugated bilirubin levels |
Countries
Germany
Outcome results
None listed