Status:
COMPLETED
HDDO-1756 Bio Equivalence Study
Lead Sponsor:
Hyundai Pharmaceutical Co., LTD.
Conditions:
Hyperlipidemias
Eligibility:
MALE
19+ years
Phase:
PHASE1
Brief Summary
For healthy adult volunteers, safety and pharmacokinetic properties are compared between the two formulations in the case of HDDO-1756 alone administration and HDDO-17561/HDDO-17562 combined administr...
Eligibility Criteria
Inclusion
- Healthy adult volunteers aged 19 or older during screening
- A person who weighs more than 50.0 kg and has a BMI of 18.0 kg/m2 or less and 30.0 kg/m2 or less.
- ☞ BMI (kg/m2) = Weight (kg) / {Long (m)}2
- A person who has no chronic disease or medical treatment and has no pathological symptoms or findings as a result of an internal examination;
- A person who has been determined to be eligible for a clinical trial according to the characteristics of the drug during screening, such as serum tests, hematologic tests, hematological tests, urine tests, urine tests, etc. and vital signs (physical tests) and 12-lead ECG tests.
Exclusion
- Current or past history of clinically significant liver, kidney, nervous system, respiratory system, endocrine system, blood and tumor, urinary system, cardiovascular system, digestive system, musculoskeletal disease, or mental illness, as well as those with the following symptoms or history:
- Patients with genetic problems such as galactose intolerance, Lapp lactase deficiency, or glucose-galactose malabsorption
- Persons with a history of gastrointestinal diseases (cron disease, ulcer, acute or chronic pancreatitis, etc.) or gastrointestinal surgery (except simple appendectomy or hernia surgery) that may affect the absorption of drugs;
Key Trial Info
Start Date :
June 12 2020
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 27 2020
Estimated Enrollment :
56 Patients enrolled
Trial Details
Trial ID
NCT04755894
Start Date
June 12 2020
End Date
July 27 2020
Last Update
February 17 2021
Active Locations (1)
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1
Hyundai Pharm
Seoul, South Korea