A Ph 1 Study of Epanova® in Healthy Chineses

Healthy Subjects Clinical Trial

Official title:

A Phase I, Open-label Study to Evaluate the Pharmacokinetics of Single and Multiple Doses of Epanova® in Chinese Healthy Subjects Living in China

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03574142
• Other study ID #: D5881C00001
• Status: Completed
• Phase: Phase 1
• Start date: June 4, 2018
• Est. completion date: June 27, 2018

Study information

• Verified date: July 2018
• Source: AstraZeneca
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to explore the safety, tolerability, and PK of single and multiple doses of Epanova in healthy male and female Chinese subjects and to allow comparison of these parameters with the Western population studied to date.

Description:

This is a single centre, open-label, single- and multiple-dose, PK study in Chinese healthy subjects. Approximately 14 subjects will receive a single oral dose of Epanova 4 g followed by a 72-hour washout period, and then receive Epanova 4 g orally once daily for 14 consecutive days. Subjects will undergo screening evaluations to determine eligibility within 4 weeks (28 days) prior to the first dose of investigational product (IP). Subjects will be admitted to the clinical pharmacology unit approximately 48 hours prior to the first dosing (Day -2) and will stay at the unit until at least 72 hours (Day 20) after their last dose of IP (Day 17). Blood samples will be collected for PK analyses. Subjects will be monitored closely for adverse events throughout the study.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 14
• Est. completion date: June 27, 2018
• Est. primary completion date: June 27, 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 45 Years

Eligibility

Inclusion Criteria:

1. Subjects must be willing and able to give written informed consent by signing an IRB-approved Informed Consent Form (ICF) prior to admission to this study and follow the restrictions and procedures outlined for the study.

2. Healthy adult males or females as determined by medical history, physical examination, and laboratory tests. Subjects are to be native Chinese, 18 to 45 years of age (inclusive) at the time of consent.

3. Body mass index (BMI) =19 and =26 kg/m2 and weigh at least 50 kg.

4. Medically healthy subjects with clinically insignificant screening results (eg, laboratory profiles, medical histories, electrocardiograms [ECGs], physical examination). Haemoglobin must be greater than the lower limit of normal. A 12-lead ECG with QTcF >340 msec and <450 msec.

5. Acceptable supine blood pressure (BP) and heart rate as determined by the investigator (systolic BP =140 mm Hg, and diastolic BP =90 mm Hg).

6. For women of childbearing potential (have not had tubal ligation, hysterectomy or surgical procedure for sterilisation), the results from a serum pregnancy test at screening and at Day -2 must be within the normal range. The subject must also agree to use an acceptable method of contraception throughout the trial. Women with an intact uterus are deemed postmenopausal if they are at least age 45, have had cessation of menses for at least 1 year, and have not taken hormones or oral contraceptives (including oestrogen or hormone replacement therapy) during the past 12 months.

Key Exclusion Criteria

1. Past history of psychological or physical disorder.

2. An individual who has abnormal laboratory values or an inappropriate current or past medical history for participation based on the PI's decision.

3. Has a history or presence of significant cardiovascular, pulmonary, hepatic, renal, haematological, gastrointestinal, endocrine, immunologic, dermatologic, neurological, or psychiatric disease.

4. Has a positive urine drug/alcohol breath testing at the screening visit or on Day -2.

5. Habitual users of drug(s) of abuse.

6. Has tested positive for human immunodeficiency virus (HIV), hepatitis B (including surface antigen [HbsAg] positive healthy carrier), hepatitis C antibodies (HCV), or syphilis.

7. Has used fish oil, other EPA and/or DHA containing supplements within 60 days of admission to the clinic.

8. Has a known sensitivity or allergy to soybeans, fish, and/or shellfish.

9. Has had a history of hypersensitivity or idiosyncratic reaction to compounds related to Epanova.

10. Pregnant or lactating women.

11. Those who have difficulty with blood sampling via a peripheral vein.

Related Conditions & MeSH terms

• Healthy Subjects

Intervention

Drug:
• Epanova
A single dose of Epanova 4 g will be administered as 4 capsules (each containing 1 g of Epanova) followed by a 72-hour washout period in Chinese healthy subjects. Subsequently, multiple doses of Epanova 4 g will be administered once daily for 14 consecutive days.

Locations

Country	Name	City	State
China	Research Site	Beijing

Sponsors (1)

Lead Sponsor	Collaborator
AstraZeneca

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	1. Plasma concentrations versus time profile of EPA and DHA	To evaluate the PK of single and multiple oral doses of Epanova in Chinese healthy subjects	Blood sample will be collected on Day-1, Day1(-1h, -5min Pre-dose and 1h, 2h, 3h, 4h, 5h, 6h, 7.5h, 9h, 12h, 16h Post-dose),Day2,3,4,7,11,14,16,and Day17 (-5min Pre-dose, 1h, 2h, 3h, 4h, 5h, 6h, 7.5h, 9h, 12h, 16h Post-dose), Day18,19 and Day20
Primary	2. Observed maximum plasma concentration (Cmax)	To evaluate the PK of single and multiple oral doses of Epanova in Chinese healthy subjects	Blood sample will be collected on Day-1, Day1(-1h, -5min Pre-dose and 1h, 2h, 3h, 4h, 5h, 6h, 7.5h, 9h, 12h, 16h Post-dose),Day2,3,4,7,11,14,16,and Day17 (-5min Pre-dose, 1h, 2h, 3h, 4h, 5h, 6h, 7.5h, 9h, 12h, 16h Post-dose), Day18,19 and Day20
Primary	3. Time to reach maximum plasma concentration (tmax)	To evaluate the PK of single and multiple oral doses of Epanova in Chinese healthy subjects	Blood sample will be collected on Day-1, Day1(-1h, -5min Pre-dose and 1h, 2h, 3h, 4h, 5h, 6h, 7.5h, 9h, 12h, 16h Post-dose),Day2,3,4,7,11,14,16,and Day17 (-5min Pre-dose, 1h, 2h, 3h, 4h, 5h, 6h, 7.5h, 9h, 12h, 16h Post-dose), Day18,19 and Day20
Primary	4. Terminal half-life	To evaluate the PK of single and multiple oral doses of Epanova in Chinese healthy subjects	Blood sample will be collected on Day-1, Day1(-1h, -5min Pre-dose and 1h, 2h, 3h, 4h, 5h, 6h, 7.5h, 9h, 12h, 16h Post-dose),Day2,3,4,7,11,14,16,and Day17 (-5min Pre-dose, 1h, 2h, 3h, 4h, 5h, 6h, 7.5h, 9h, 12h, 16h Post-dose), Day18,19 and Day20
Primary	5. Area under the plasma concentration-time curve from time zero to time of last quantifiable analyte concentration (AUC0-t)), from time zero to 24 hours (AUC0-24h), and from time zero extrapolated to infinity (AUC)	To evaluate the PK of single and multiple oral doses of Epanova in Chinese healthy subjects	Blood sample will be collected on Day-1, Day1(-1h, -5min Pre-dose and 1h, 2h, 3h, 4h, 5h, 6h, 7.5h, 9h, 12h, 16h Post-dose),Day2,3,4,7,11,14,16,and Day17 (-5min Pre-dose, 1h, 2h, 3h, 4h, 5h, 6h, 7.5h, 9h, 12h, 16h Post-dose), Day18,19 and Day20
Primary	6. Apparent clearance for parent drug estimated as dose divided by AUC (CL/F)	To evaluate the PK of single and multiple oral doses of Epanova in Chinese healthy subjects	Blood sample will be collected on Day-1, Day1(-1h, -5min Pre-dose and 1h, 2h, 3h, 4h, 5h, 6h, 7.5h, 9h, 12h, 16h Post-dose),Day2,3,4,7,11,14,16,and Day17 (-5min Pre-dose, 1h, 2h, 3h, 4h, 5h, 6h, 7.5h, 9h, 12h, 16h Post-dose), Day18,19 and Day20
Secondary	Number of subjects with adverse events.	Following categories will be collected and analyzed: any adverse event (AE), any AE causally related to investigational product (IP), serious adverse events (SAEs), SAEs causally related to IP, AEs with outcome of death, AEs leading to discontinuation of IP, and other significant AEs.	Adverse event will be collected from Visit 4(Day1) to Visit 23 (Day20).
Secondary	Safety as determined by evaluation of blood pressure in mmHg	Measurement of blood pressure (systolic and diastolic in mmHg)	Blood presure will be collected from Visit1(any day between Day-28 to Day-2) to Visit23(Day20).
Secondary	Safety as determined by evaluation of heart beat in beats per minute	Measurement of heart beat in beats per minute	Heart beat will be collected from Visit1(any day between Day-28 to Day-2) to Visit23(Day20).
Secondary	Safety as determined by evaluation of body temperature in degree Celsius	Measurement of body temperature in degree Celsius	Body temperature will be collected from Visit1(any day between Day-28 to Day-2) to Visit23(Day20).
Secondary	Safety as determined by evaluation of respiratory rate in breaths per minute	Measurement of respiratory rate in breaths per minute	Respiratory rate will be collected from Visit1(any day between Day-28 to Day-2) to Visit23(Day20).
Secondary	Safety as determined by analysis of electrocardiograms	Analysis of 12-lead electorcardiograms	Electrocardiograms will be collected at Visit1(any day between Day-28 to Day-2), Visit3(Day-1) and V23(Day20).
Secondary	Safety as determined by abnormality in haematology	Measurement of red blood cell count, white blood cell count, haemoglobin and platelets	Blood samples will be collected at Visit1(any day between Day-28 to Day-2), Visit2 (Day -2) and Visit23(Day20).
Secondary	Safety as determined by abnormality in clinical chemistry	Measurement of kidney function (e.g.urea ,creatinine, Uric acid), liver function(ALP, ALT, AST, albumin, total bilirubin, direct bilirubin), lipid profile(total cholesterol, triglycerides), potassium and hs-CRP	Blood samples will be collected at Visit1(any day between Day-28 to Day-2), Visit2 (Day -2) and Visit23(Day20).
Secondary	Safety as determined by abnormality in urinalysis	Measurement of leucocyte, red blood cells, protein and microscopy	Urine samples will be collected at Visit1(any day between Day-28 to Day-2), Visit2 (Day -2) and Visit23(Day20).