A Study to Assess the Pharmacokinetics and Food Effect of SR419 in Healthy Subjects

NCT ID: NCT04705077

Last Updated: 2021-03-25

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 24 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-02-02
• Study Completion Date: 2021-03-12

Brief Summary

This will be an open-label, single-site, Phase I study to evaluate the PK, safety, and tolerability of SR419 in healthy volunteers.

Detailed Description

This study is a phase 1, open-label study to assess the single dose pharmacokinetics of suspension and capsule formulations of SR419 and repeat dose pharmacokinetics of capsule formulation of SR419, and to assess the effect of a high-fat meal on the pharmacokinetics of SR419 in healthy subjects.The trial will consist of 3 cohorts. Cohort 1 and 2 will follow a single sequence, 3-period, 2-formulation, dosing in fasted or fed state design. Cohort 3 will be a repeated dose study of SR419 capsule in healthy subjects.

Conditions

Healthy

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SEQUENTIAL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Single Dose Treatment

Each subject will be assigned to the fixed period sequence.

• Period 1: SR419 suspension in the fasted state;
• Period 2: SR419 capsule in the fasted state;
• Period 3: SR419 capsule in the fed state (high-fat meal).

Group Type: EXPERIMENTAL

SR419

Intervention Type: DRUG

2 formulations of SR419, SR419 suspension and SR419 capsule will be used in the study.

Repeated Dose Treatment

Each subject will receive 30 mg of SR419 capsule, once every 8 hours (Q8h), for 5 days.

Group Type: EXPERIMENTAL

SR419

Intervention Type: DRUG

2 formulations of SR419, SR419 suspension and SR419 capsule will be used in the study.

Interventions

SR419

2 formulations of SR419, SR419 suspension and SR419 capsule will be used in the study.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Healthy males or females who are 18 to 64 years of age inclusive, are eligible.

2. Body weight > 50 kg (110 pounds) and body mass index (BMI) between 18 and 30 kg/m2.

3. Male or female subjects must agree to use contraception methods.

4. Capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.

Exclusion Criteria

1. Clinically significant history of central nervous system (CNS) disease.

2. Current or chronic history of liver disease or known hepatic or biliary abnormalities

3. History of regular alcohol consumption within 6 months of screening defined as: an average weekly intake of >21 units for males or >14 units for females. One unit is equivalent to 8 g of alcohol: a half-pint (~285 mL) of beer, 1 glass (125 mL) of wine or 1 measure (25 mL) of spirits.

4. History of significant drug abuse within one year of screening or use of soft drugs (such as marijuana) within 3 months prior to screening or hard drugs (such as cocaine, methamphetamine, crack) within 1 year prior to screening.

5. History of sensitivity to any of the components thereof or a history of drug or other allergy that, in the opinion of the Investigator or Medical Monitor, contraindicates participation.

6. History of asthma (excluding resolved childhood asthma), anaphylaxis or anaphylactoid reactions, severe allergic responses.

7. History of hypercoagulable state or history of thrombosis.

8. A positive Hepatitis B surface antigen, Hepatitis C antibody or human immunodeficiency virus (HIV) antibody result.

9. A positive urinary cotinine test or history of regular use of tobacco- or nicotine-containing products (more than 4 products per month within 6 months prior to screening) or unwilling to refrain from use of such products from Screening until completion of the final study visit.

10. A positive drug/alcohol result.

11. The subject has participated in a clinical trial and has received an investigational product within the following time period prior to the first dosing day in the current study: 30 days, 5 half-lives or twice the duration of the biological effect of the investigational product (whichever is longer).

12. Unable to refrain from consumption of Seville oranges, grapefruit or grapefruit juice within 7 days prior to the first dose of IMP until the Safety Follow-up visit.

13. A positive pregnancy test result.

14. Breast-feeding and/or lactating subject.

15. Any reason which, in the opinion of the Investigator, would prevent the subject from participating in the study.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 64 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

SIMR (Australia) Biotech Pty Ltd.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Thomas Polasek

Role: PRINCIPAL_INVESTIGATOR

CMAX Clinical Research

Locations

CMAX Clinical Research

Adelaide, , Australia

Countries

Australia

Other Identifiers

SR419-103

Identifier Type: -

Identifier Source: org_study_id