Bioequivalence Study Between "Dong-A Atorvastatin Tab" and "Lipitor Tab"

Healthy Clinical Trial

Official title:

A Open-Label, Randomized, 2-sequence, 4-period, Fasting Condition, Singledose, Per Oral, Cross-over Study to Evaluate the Bioequivalence Between "Dong-A Atorvastatin 80mg Tab" and "Lipitor 80mg Tab" in Healthy Volunteers

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04325009
• Other study ID #: DDS19-066BE
• Status: Recruiting
• Phase: Phase 1
• Start date: March 30, 2020
• Est. completion date: August 2020

Study information

• Verified date: March 2020
• Source: Dong-A ST Co., Ltd.
• Contact: SeungHyun Kang, Ph.D
• Phone: 82-070-4665-9490
• Email: juspa[@]naver.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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

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

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 56
• Est. completion date: August 2020
• Est. primary completion date: May 2020
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 19 Years and older

Eligibility

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

Related Conditions & MeSH terms

• Healthy

Intervention

Drug:
• Lipitor 80mg Tab ? Dong-A Atorvastatin 80mg Tab
st period: single oral administration of 1 tablet of "Lipitor 80mg Tab" washout period: 7days nd period: single oral administration of 1 tablet of "Dong-A Atorvastatin 80mg Tab" washout period: 7days rd period: single oral administration of 1 tablet of "Lipitor 80mg Tab" washout period: 7days th period: single oral administration of 1 tablet of "Dong-A Atorvastatin 80mg Tab"
• Dong-A Atorvastatin 80mg Tab ? Lipitor 80mg Tab
st period: single oral administration of 1 tablet of "Dong-A Atorvastatin 80mg Tab" washout period: 7days nd period: single oral administration of 1 tablet of "Lipitor 80mg Tab" washout period: 7days rd period: single oral administration of 1 tablet of "Dong-A Atorvastatin 80mg Tab" washout period: 7days th period: single oral administration of 1 tablet of "Lipitor 80mg Tab"

Locations

Country	Name	City	State
Korea, Republic of	H Plus Yangji Hospital	Seoul

Sponsors (1)

Lead Sponsor	Collaborator
Dong-A ST Co., Ltd.

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Area Under the plasma Concetration versus time curve(AUCt) of Atorvastatin	Area Under the plasma Concetration versus time curve(AUCt) of Atorvastatin	Before administration ~ 36hrs
Primary	Peak Plasma Concentration(Cmax) of Atorvastatin	Peak Plasma Concentration(Cmax) of Atorvastatin	Before administration ~ 36hrs