A Phase 1 Study to Evaluate the Safety and Pharmacokinetics of Ezerosu Tab

NCT06225635 | Completed Phase 1

• 1 other identifier: SP-RE-HYP-101
• Study Type: interventional
• Target: 60
• Locations: 1 country
• Sites: 1

Brief Summary

A Phase 1 Study to Evaluate the Safety and Pharmacokinetics of Ezerosu Tab

Conditions

Hyperlipidemias

Keywords

Arteriosclerosis; Primary Hypercholesterolemia; Hyperlipidemias

Outcome Measures

Primary Outcomes (2)

• Cmax of Total Ezetimibe, Rosuvastatin

  Cmax of Total Ezetimibe, Rosuvastatin

  follow up to Day8

• AUCt of Total Ezetimibe, Rosuvastatin

  AUCt of Total Ezetimibe, Rosuvastatin

  follow up to Day8

Secondary Outcomes (5)

• AUC∞ of Total Ezetimibe, Rosuvastatin and AUC∞ of Free Ezetimibe

  follow up to Day8

• Tmax of Total Ezetimibe, Rosuvastatin and Tmax of Free Ezetimibe

  follow up to Day8

• t1/2 of Total Ezetimibe, Rosuvastatin and t1/2 of Free Ezetimibe

  follow up to Day8

• Cmax of Free Ezetimibe

  follow up to Day8

• AUCt of Free Ezetimibe

  follow up to Day8

Study Arms (2)

Test

EXPERIMENTAL

Ezerosu tablet(double layer tablet)

Drug: Ezerosu(monolayer tablet); Drug: Ezerosu(double layer tablet)

Control

ACTIVE COMPARATOR

Ezerosu tablet(monolayer tablet)

Drug: Ezerosu(monolayer tablet); Drug: Ezerosu(double layer tablet)

Interventions

Ezerosu(monolayer tablet) DRUG

Ezetimibe 10mg, Rosuvastatin calcium 20.8mg(20mg as Rosuvastatin)

Control; Test

Ezerosu(double layer tablet) DRUG

Ezetimibe 10mg, Rosuvastatin calcium 20.8mg(20mg as Rosuvastatin)

Control; Test

Eligibility Criteria

• Age: 19 Years+
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Those who are 19 years old or older at the time of the screening visit
• At the time of screening visit, those who weigh 50 kg or more for men, 45 kg or more for women, and have a body mass index (BMI) of 18.0 kg / m2 or more and 30.0 kg / m2 or less.
• ☞ BMI (kg / m2) = Weight (kg) / {Height (m)} 2
• Those who have no clinically significant congenital or chronic illness at the time of the screening visit and have no medical examination results, pathological symptoms or findings.
• Diagnostic tests such as hematology tests, blood chemistry tests, serum tests, urine tests, and electrocardiogram test result tests set and performed by the test director (or the commissioned doctor in charge of the test) according to the characteristics of the clinical test drug. Now that it has been determined to fit the subject
• Clinical trial drug From the first dosing date to the last clinical trial drug 14 days from the dosing date, the person, sperm, or partner should use medically appropriate contraceptive methods \* to eliminate the possibility of pregnancy. Agree and agree not to donate sperm or eggs
• \* Contraceptives: Combined use or killing of intrauterine devices, sperm surgery, tubal contraception and blockage contraceptives (male condoms, female condoms, cervical caps, contraceptive diaphragms, sponges, etc.) When using spermicide, use two or more contraceptive methods as a combination
• A person who has signed a consent form by a free doctor after listening to and understanding the purpose and content of this clinical trial, the characteristics of the drug for clinical trial, expected abnormal reactions, etc.

You may not qualify if:

• Digestive system, cardiovascular system, endocrine system, respiratory system, blood / tumor, infectious disease, kidney and urogenital system, psychiatric / nervous system, musculoskeletal system, immune system, otolaryngology, dermatology, ophthalmology People with clinically significant illness or past strength who fall into the system
• Those who have past ability of gastrointestinal surgery (excluding simple appendectomy and hernia surgery) that can affect drug absorption, or have gastrointestinal illness
• Those who took drug-metabolizing enzyme-inducing and inhibitory drugs such as barbital drugs within 1 month of the first dosing date, or took drugs that may interfere with this clinical study within 10 days of the first dosing date (however) , Interaction with clinical study drugs, half-life of concomitant drugs, etc. Can be participated in consideration of drug dynamics and pharmacodynamics)
• Those who participated in other clinical trials or bioequivalence studies and received clinical trial drugs within 6 months of the first dosing date.
• Those who donated whole blood or component blood within 2 weeks or received blood transfusion within 4 weeks on the first dosing day
• Those who meet the following conditions within one month of the first dosing date
• For men, alcohol intake exceeding 21 cups / week on average
• For females, alcohol intake exceeding 14 cups / week on average
• (1 cup = 50 mL of shochu or 30 mL of Western liquor or 250 mL of beer)
• Smoking an average of 20 cigarettes or more per day
• Those who fall under the following
• ・ Persons with hypersensitivity to the main ingredients or constituents of this drug
• Persons with genetic problems such as galactose intolerance, Lapp lactase deficiency or glucose-galactose malabsorption
• Patients with the following diseases
• Patients with active liver disease or patients with persistently high symptoms due to unknown causes of serum amino transduction enzyme levels

Sponsors & Collaborators

• Shin Poong Pharmaceutical Co. Ltd.: lead

Study Sites (1)

H Plus Yangji Hospital

Seoul, South Korea

Location

MeSH Terms

Conditions

Hyperlipidemias; Arteriosclerosis

Condition Hierarchy (Ancestors)

Dyslipidemias; Lipid Metabolism Disorders; Metabolic Diseases; Nutritional and Metabolic Diseases; Arterial Occlusive Diseases; Vascular Diseases; Cardiovascular Diseases

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: CROSSOVER
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: December 13, 2021
• First Posted: January 26, 2024
• Study Start: January 1, 2022
• Primary Completion: March 7, 2022
• Study Completion: March 7, 2022
• Last Updated: January 26, 2024

Record last verified: 2022-03

Locations

KR (1)