Status:
UNKNOWN
Clinical Study to Investigate the PK Profiles and Safety of CKD-385 in Healthy Volunteers Under Fasting Conditions
Lead Sponsor:
Chong Kun Dang Pharmaceutical
Conditions:
Cardiovascular Diseases
Eligibility:
All Genders
19+ years
Phase:
PHASE1
Brief Summary
Clinical Study to Investigate the Pharmacokinetic Profiles and Safety of High-dose CKD-385 in Healthy Volunteers under Fasting Conditions
Detailed Description
A randomized, open-label, single dose, crossover study to investigate the pharmacokinetic profiles and safety of high-dose CKD-385 in healthy volunteers under fasting conditions
Eligibility Criteria
Inclusion
- Healthy adult aged more than 19 at the time of screening
- Those who had 18.0kg/m² ≤ Body Mass Index (BMI) \< 30.0kg/m²
- \# BMI=Weight(kg) / Height(m)²
- Those who have no congenital diseases or chronic diseases and have no abnormal symptoms or findings on a medical examination.
- Those who are eligible for clinical trials based on laboratory (hematology, blood chemistry, urinalysis, serology), vital signs and ECG results at screening.
- Those who have voluntarily given written informed consents to participate in the study and to comply with all the instructions, based on full understanding of the nature of the study after listening to detailed explanations.
- Those who agree to double contraception method from the 1st administration of the investigational product until 7 days after the last administration of investigational product.
Exclusion
- Those who has medical evidence or history of clinically significant hematological, renal, endocrine, pulmonary, gastrointestinal, urinary, cardiovascular, hepatic, psychiatric, neurologic or allergic diseases(except for simple dental history such as tartar, impacted teeth, wisdom teeth).
- Those with a medical history of gastrointestinal disorders(esophageal achalasia or esophagus stenosis, Crohn's disease) or gastrointestinal surgery(except for simple appendicitis surgery or hernia surgery or tooth extraction surgery) that may affect the absorption of drug.
- Those who has a history of regular alcohol consumption in excess of 14 glasses/week for woman, 21 glasses/week for man within 1 months prior to screening.
- Those who received investigational products or bioequivalence test drugs within 6 months before the first administration of clinical trial drugs.
- Those who take drugs which may cause induction or inhibition of drug metabolism within 30 days before the first administration of investigational products.
- Those who have taken any drugs that may affect the clinical trial within 10 days.
- Those who donated whole blood within 2 months, or blood components within 2 week before first administration of investigational products.
- Those who are deemed insufficient to participate in this clinical study by investigators.
Key Trial Info
Start Date :
October 29 2020
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 12 2020
Estimated Enrollment :
24 Patients enrolled
Trial Details
Trial ID
NCT04678388
Start Date
October 29 2020
End Date
December 12 2020
Last Update
December 21 2020
Active Locations (1)
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1
Central Hospital
Gyeonggi-do, Siheung-si, South Korea, 15079