A Bioavailability and Food Effect Study of AZD5462 in Healthy Volunteers

Healthy Participants Clinical Trial

Official title:

A Randomized, 6-period, 6-treatment, Single-Dose, Crossover Study to Assess the Pharmacokinetics of AZD5462 Film-coated Tablet Formulation, to Assess the Relative Bioavailability of AZD5462 Film-coated Tablet Formulation vs Oral Solution, and to Assess the Influence of Food on the Pharmacokinetics of AZD5462 in Healthy Participants

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05512806
• Other study ID #: D9090C00005
• Status: Completed
• Phase: Phase 1
• Start date: August 24, 2022
• Est. completion date: November 7, 2022

Study information

• Verified date: October 2023
• Source: AstraZeneca
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study will assess the pharmacokinetics of AZD5462 film-coated tablet formulation in healthy participants.

Description:

This study will consist of six treatment periods.

A total of 16 healthy male and female participants of non-childbearing potential will be randomized in this study to ensure at least 12 evaluable participants at the end of the last treatment period.

The study will comprise of a Screening Period, six Treatment Periods, and a follow-up phone call:

• A screening period of maximum 28 days.

• Six treatment periods during which participants will be residents at the study center from Day -1 until Day 17.

Each participant will receive 6 treatments.

The following treatments will be given:-

• Treatment A: Dose A of AZD5462 film-coated tablet in a fasted state.

• Treatment B: Dose A of AZD5462 film-coated tablet in a fed state.

• Treatment C: Dose B of AZD5462 film-coated tablet in a fasted state.

• Treatment D: Dose B of AZD5462 oral solution in a fasted state.

• Treatment E: Dose C of AZD5462 film-coated tablet in a fasted state.

• Treatment F: Dose C of AZD5462 film-coated tablet in a fed state.

• A follow-up phone call will take place on Day 21 (± 1 day) to record adverse events (AEs) and concomitant medication.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 16
• Est. completion date: November 7, 2022
• Est. primary completion date: November 7, 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria:

• Provision of signed and dated, written informed consent prior to any study specific procedures.

• Healthy male and female participants aged 18 to 55 years at screening and admission with suitable veins for cannulation or repeated venipuncture.

• Females must have a negative pregnancy test at screening and on admission to the study center, must not be lactating and must be of non-childbearing potential confirmed at screening by fulfilling one of the following criteria:

1. Postmenopausal defined as amenorrhea for at least 12 months or more following cessation of all exogenous hormonal treatments and Follicle-stimulating hormone (FSH)/Luteinizing hormone (LH) levels in the postmenopausal range.

2. Documentation of irreversible surgical sterilization by hysterectomy, bilateral oophorectomy or bilateral salpingectomy but not tubal ligation.

• Male participant must adhere to the contraception methods details.

• Have a Body mass index (BMI) between 18 and 32 kg/m2 inclusive and weigh at least 50 kg and no more than 105 kg inclusive at screening.

Exclusion Criteria:

• History of any clinically significant disease or disorder which may either put the participant at risk because of participation in the study, or influence the results or the participant's ability to participate in the study.

• Any of the below conditions:

1. Systemic sclerosis.

2. Moderate to severe valvular disease.

3. Hypertrophic obstructive cardiomyopathy.

4. Restrictive cardiomyopathy.

5. Gilbert's syndrome.

6. History of vascular or left ventricular aneurysms, or prior dissections.

7. Any history of joint hypermobility, Marfan's Syndrome, or any connective tissue disorder.

• History or presence of gastrointestinal, hepatic or renal disease, or any other condition known to interfere with absorption, distribution, metabolism, or excretion of drugs.

• Any clinically significant illness, medical/surgical procedure, or trauma within 4 weeks of the first administration of Investigational medicinal product (IMP).

• Any laboratory values with the following deviations at screening, or admission to the study center:

1. Total bilirubin > Upper limit of normal (ULN).

2. Alanine aminotransferase > 1.5 × ULN.

3. Aspartate aminotransferase > 1.5 × ULN.

4. Estimated glomerular filtration rate (eGFR) < 90 mL/min/1.73m2, as assessed by the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) formula.

5. White blood cell count < 3.5 k/uL and > ULN.

6. Hemoglobin < Lower limit of normal (LLN).

• Any clinically significant abnormalities in clinical biochemistry, hematology, or urinalysis results.

• Any clinically significant abnormal findings in vital signs after 5 minutes supine rest, at screening or admission defined as any of the following:

1. Systolic Blood pressure (BP) < 90 mmHg or = 140 mmHg.

2. Diastolic BP < 50 mmHg or = 90 mmHg.

3. Heart rate < 50 bpm or > 90 bpm.

• Any clinically important abnormalities in rhythm, conduction or morphology of the resting 12-lead Electrocardiogram (ECG) at screening or admission.

1. Prolonged QTcF > 450 ms.

2. Shortened QTcF < 340 ms.

3. Family history of long QT syndrome.

4. PR(PQ) interval shortening < 120 ms (PR > 110 ms but < 120 ms is acceptable if there is no evidence of ventricular pre-excitation).

5. PR(PQ) interval prolongation (> 240 ms) intermittent second (Wenckebach block while asleep is not exclusive) or third-degree AV block, or AV dissociation.

6. Persistent or intermittent complete BBB. Participants with Intraventricular conduction delay (IVCD) with QRS < 120 ms are acceptable if there is no evidence of eg, ventricular hypertrophy, or pre-excitation.

• Any positive result on screening for serum hepatitis B surface antigen, hepatitis C antibody, and Human immunodeficiency virus (HIV) antibody.

• Known or suspected history of drug abuse.

• Has received another new chemical entity within 30 days of the first administration of IMP in this study.

• Plasma donation within 1 month of screening or any blood donation/loss > 500 mL during the 3 months prior to screening.

• History of severe allergy/hypersensitivity or ongoing allergy/hypersensitivity, or history of hypersensitivity to drugs with a similar chemical structure or class to AZD5462.

• Current smokers or those who have smoked or used nicotine products within the 3 months prior to screening.

• Positive screen for drugs of abuse, alcohol, or cotinine at screening or on each admission to the study center prior to the first administration of the IMP.

• Use of drugs with enzyme-inducing properties such as St John's Wort within 3 weeks prior to the first administration of IMP.

• Use of any prescribed or non-prescribed medication including antacids, analgesics, herbal remedies, megadose vitamins, and minerals during the 2 weeks or 5 half-lives of the medication, whichever is longer, prior to the first administration of IMP.

• Known or suspected history of alcohol or drug abuse or excessive intake of alcohol.

• Excessive intake of caffeine-containing drinks or food.

• Participants who have previously received AZD5462.

• Any ongoing or recent minor medical complaints that may interfere with the interpretation of study data or are considered unlikely to comply with study procedures, restrictions, and requirements.

• Participants who are vegans or have medical dietary restrictions.

• Participants who cannot communicate reliably with the Principal Investigator (PI).

• Vulnerable participants, eg, kept in detention, protected adults under guardianship, trusteeship, or committed to an institution by governmental or juridical order.

• Clinical signs and symptoms consistent with Coronavirus disease 2019 (COVID-19), or confirmed infection by appropriate laboratory test within the last 4 weeks prior to screening or on admission.

Related Conditions & MeSH terms

• Healthy Participants

Intervention

Drug:
• AZD5462
Participants will receive AZD5462 orally.

Locations

Country	Name	City	State
United States	Research Site	Brooklyn	Maryland

Sponsors (2)

Lead Sponsor	Collaborator
AstraZeneca	Parexel

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Area under plasma concentration time curve from zero to infinity (AUCinf)	The AUCinf of a film-coated tablet of AZD5462 at 3 dose levels will be assessed.	Day 1 to Day 17
Primary	Area under the plasma concentration-curve from time zero to last quantifiable concentration (AUClast)	The AUClast of a film-coated tablet of AZD5462 at 3 dose levels will be assessed.	Day 1 to Day 17
Primary	Maximum observed plasma (peak) drug concentration [Cmax]	The Cmax of a film-coated tablet of AZD5462 at 3 dose levels will be assessed.	Day 1 to Day 17
Primary	Area under plasma concentration time curve from zero to infinity (AUCinf)	The effect of a high-fat, high-calorie meal in comparison to fasting conditions on the AUCinf of AZD5462 after a single oral dose at 2 dose levels will be assessed.	Day 1 to Day 17
Primary	Area under the plasma concentration-curve from time zero to last quantifiable concentration (AUClast)	The effect of a high-fat, high-calorie meal in comparison to fasting conditions on the AUClast of AZD5462 after a single oral dose at 2 dose levels will be assessed.	Day 1 to Day 17
Primary	Maximum observed plasma (peak) drug concentration [Cmax]	The effect of a high-fat, high-calorie meal in comparison to fasting conditions on the Cmax of AZD5462 after a single oral dose at 2 dose levels will be assessed.	Day 1 to Day 17
Primary	Area under plasma concentration time curve from zero to infinity (AUCinf)	The relative bioavailability of the film-coated tablet vs oral solution formulation will be determined by the assessment of AUCinf.	Day 1 to Day 17
Primary	Area under the plasma concentration-curve from time zero to last quantifiable concentration (AUClast)	The relative bioavailability of the film-coated tablet vs oral solution formulation will be determined by the assessment of AUClast.	Day 1 to Day 17
Primary	Maximum observed plasma (peak) drug concentration [Cmax]	The relative bioavailability of the film-coated tablet vs oral solution formulation will be determined by the assessment of Cmax.	Day 1 to Day 17
Secondary	Number of participants with Adverse Events (AEs), and Serious Adverse Events (SAEs)	The safety, and tolerability of single doses of AZD5462 in healthy participants will be assessed.	Until follow-up (Day 21)