Healthy
Conditions
Brief summary
An Open-Label, Randomized, 2-sequence, 4-period, Fasting Condition, Single-dose, Per Oral, Cross-over Study to Evaluate the Bioequivalence between Dong-A Atorvastatin 80mg Tab and Lipitor 80mg Tab in Healthy Volunteers
Detailed description
1. Study design: An open-Label, randomized, 2-sequence, 4-period, fasting condition, single-dose, per oral, cross-over study 2. Administration method: The subject should maintain a minimum of 10 hours of empty stomach before administration, and give an oral dose of 1 tablets (Dong-A Atorvastatin 80mg or Lipitor 80mg) with 150 mL of water at around 8 a.m. on the day of the test. The subject should not chew or break the drug, but should swallow in whole with water. The difference in administration time between the test subjects is about one minute apart, considering the blood collection time. 3. Wash out period: at least 7 days 4. Blood collection time: Before the administration, 0.17, 0.33, 0.5, 0.75, 1, 1.33, 1.67, 2, 3, 4, 6, 8, 12, 24, 36 hr after the administration (total 16 times) 5. Analysis: Measurement of the concentration of an unchangeable substance of Atorvastatin in plasma
Interventions
DRUGLipitor 80mg Tab → Dong-A Atorvastatin 80mg Tab
1. st period: single oral administration of 1 tablet of Lipitor 80mg Tab washout period: 7days 2. nd period: single oral administration of 1 tablet of Dong-A Atorvastatin 80mg Tab washout period: 7days 3. rd period: single oral administration of 1 tablet of Lipitor 80mg Tab washout period: 7days 4. th period: single oral administration of 1 tablet of Dong-A Atorvastatin 80mg Tab
DRUGDong-A Atorvastatin 80mg Tab → Lipitor 80mg Tab
1. st period: single oral administration of 1 tablet of Dong-A Atorvastatin 80mg Tab washout period: 7days 2. nd period: single oral administration of 1 tablet of Lipitor 80mg Tab washout period: 7days 3. rd period: single oral administration of 1 tablet of Dong-A Atorvastatin 80mg Tab washout period: 7days 4. th period: single oral administration of 1 tablet of Lipitor 80mg Tab
Sponsors
Dong-A ST Co., Ltd.
Study design
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
NONE
Intervention model description
Crossover Assignment single-dose, 2-sequence, 4-period Bioequivalence Study
Eligibility
Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
1. A person who aged 19 or older at the time of screening 2. BMI of 18 to 30 (BMI calculation: kg/m2) * Males weighing 50kg or more * Females weighing 45kg or more 3. No congenital or chronic diseases or pathological symptoms 4. A person who is judged to be suitable for the study by the investigator based on the clinical laboratory examination 5. A person who has fully understood the contents of the consent form for the study and signed the consent form voluntarily and recorded the date of signature 6. A person who agreed to use contraception from the first administration of IP to a week after the last administration of IP
Exclusion criteria
1. A person who has taken a drug that significantly induces (e.g., barbital) or inhibits the drug metabolic enzyme within 30 days prior to the first administration of IP 2. A person who has participated in other clinical trials within six months prior to the first administration of the IP 3. A person who has had whole blood transfusion within 2 months or the apheresis within 2 weeks before the first administration of IP 4. A person who has medical history of gastric resection that can affect the drug absorption 5. A person with a history of regular alcohol intake within a month prior to the first administration of the IP: * Male: More than 21 cups/week * Female: More than 14 cups/week (1 cup: 50 ml of soju, 250 ml of beer, 30ml of spirits) 6. A person who is hypersensitive to any of the IP components, taking glecaprevir, pibrentasvir, has active hepatic disease, Blood AST (GOT) or ALT (GPT) levels exceed the upper reference range limit by 3 times, muscle disease, or any genetic symtoms such as galactose intolerance, Lapp lactase deficiency or glucose-galactose malabsorption 7. A person who has medical history of mental disease 8. A person who is judged not to be suitable for the study by the investigator 9. Lactating or possibly pregnant women
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Area Under the plasma Concetration versus time curve(AUCt) of Atorvastatin | Before administration ~ 36hrs | Area Under the plasma Concetration versus time curve(AUCt) of Atorvastatin |
| Peak Plasma Concentration(Cmax) of Atorvastatin | Before administration ~ 36hrs | Peak Plasma Concentration(Cmax) of Atorvastatin |
Countries
South Korea
Contacts
Primary ContactSeungHyun Kang, Ph.D
Outcome results
None listed