A Phase I, Open-label Study to Evaluate the Pharmacokinetics of Single and Multiple Doses of Epanova® in Chinese Healthy Subjects Living in China
Overview
- Phase
- Phase 1
- Intervention
- Epanova
- Conditions
- Healthy Subjects
- Sponsor
- AstraZeneca
- Enrollment
- 14
- Locations
- 1
- Primary Endpoint
- 1. Plasma concentrations versus time profile of EPA and DHA
- Status
- Completed
- Last Updated
- 7 years ago
Overview
Brief 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.
Detailed 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.
Investigators
Eligibility Criteria
Inclusion Criteria
- •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.
- •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.
- •Body mass index (BMI) ≥19 and ≤26 kg/m2 and weigh at least 50 kg.
- •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.
- •Acceptable supine blood pressure (BP) and heart rate as determined by the investigator (systolic BP ≤140 mm Hg, and diastolic BP ≤90 mm Hg).
- •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
- •Past history of psychological or physical disorder.
- •An individual who has abnormal laboratory values or an inappropriate current or past medical history for participation based on the PI's decision.
- •Has a history or presence of significant cardiovascular, pulmonary, hepatic, renal, haematological, gastrointestinal, endocrine, immunologic, dermatologic, neurological, or psychiatric disease.
Exclusion Criteria
- Not provided
Arms & Interventions
Epanova
Epanova® capsule, per oral
Intervention: Epanova
Outcomes
Primary Outcomes
1. Plasma concentrations versus time profile of EPA and DHA
Time Frame: 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
To evaluate the PK of single and multiple oral doses of Epanova in Chinese healthy subjects
4. Terminal half-life
Time Frame: 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
To evaluate the PK of single and multiple oral doses of Epanova in Chinese healthy subjects
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)
Time Frame: 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
To evaluate the PK of single and multiple oral doses of Epanova in Chinese healthy subjects
6. Apparent clearance for parent drug estimated as dose divided by AUC (CL/F)
Time Frame: 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
To evaluate the PK of single and multiple oral doses of Epanova in Chinese healthy subjects
2. Observed maximum plasma concentration (Cmax)
Time Frame: 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
To evaluate the PK of single and multiple oral doses of Epanova in Chinese healthy subjects
3. Time to reach maximum plasma concentration (tmax)
Time Frame: 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
To evaluate the PK of single and multiple oral doses of Epanova in Chinese healthy subjects
Secondary Outcomes
- Number of subjects with adverse events.(Adverse event will be collected from Visit 4(Day1) to Visit 23 (Day20).)
- Safety as determined by evaluation of blood pressure in mmHg(Blood presure will be collected from Visit1(any day between Day-28 to Day-2) to Visit23(Day20).)
- Safety as determined by evaluation 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).)
- Safety as determined by evaluation of body temperature in degree Celsius(Body temperature will be collected from Visit1(any day between Day-28 to Day-2) to Visit23(Day20).)
- Safety as determined by evaluation 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).)
- Safety as determined by analysis of electrocardiograms(Electrocardiograms will be collected at Visit1(any day between Day-28 to Day-2), Visit3(Day-1) and V23(Day20).)
- Safety as determined by abnormality in haematology(Blood samples will be collected at Visit1(any day between Day-28 to Day-2), Visit2 (Day -2) and Visit23(Day20).)
- Safety as determined by abnormality in clinical chemistry(Blood samples will be collected at Visit1(any day between Day-28 to Day-2), Visit2 (Day -2) and Visit23(Day20).)
- Safety as determined by abnormality in urinalysis(Urine samples will be collected at Visit1(any day between Day-28 to Day-2), Visit2 (Day -2) and Visit23(Day20).)