A Clinical Trial to Compare the Pharmacokinetic and Safety of CKD-828 20/1.25mg

Exclusion Criteria

• •1. Clinically significant blood, kidneys (severe renal dysfunction, etc.), endocrine, respiratory, gastrointestinal, urology, cardiovascular (within one month of severe aortic stenosis, instability, or myocardial infarction), liver (severe hepatic dysfunction, biliary obstruction, bile congestion, etc.), mental, nerve or immune disease simple dental evidence
• •2. A person who has a history of gastrointestinal diseases (e.g., esophageal diseases such as esophageal dysphagia or esophageal stenosis, Crohn's disease) or surgery (excluding simple appendectomy, hernia, or extraction surgery) that can affect drug absorption
• •3. A person who shows the following figures as a result of performing an inspection laboratory inspection during screening
• •* ALT or AST \> Twice the upper limit of the normal range
• •* CK\> 3 times the upper limit of the normal range
• •* eGFR \<60 mL/min/1.73 m2 using CKD-EPI formula
• •4. Screening Those with a history of regular alcohol consumption exceeding 210 g/week within 6 months (Beer (5%) 1 glass (250 mL) = 10 g, Soju (20%) 1 glass (50 mL) = 8 g, Wine (12%) 1 glass (125 mL) = 12 g)
• •5. Smokers with 20 or more cigarettes per day within 6 months of screening
• •6. A person who has taken another clinical trial drug or biological equivalence test drug within six months prior to the first administration of the clinical trial drug
• •7. Person who falls under the following results of vital signs measurement during screening
• •☞ Those with systolic blood pressure of less than 90 mmHg, 140 mmHg or more, or diastolic blood pressure of less than 60 mmHg or 90 mmHg or more in the sedentary state
• •8. A person who has a history of serious alcohol or drug misuse within one year of screening
• •9. A person who has taken a drug known to significantly induce or inhibit drug metabolites within 30 days prior to the first administration of a drug for clinical trials
• •10. A person who has taken prescription or non-prescription drugs within 10 days prior to the first administration of a clinical trial drug
• •11. A person who has donated all blood within two months before the first administration of a clinical trial drug, or has donated blood components within one month, or received a blood transfusion within one month
• •12. Those with severe acute/chronic medical and mental conditions that may increase risk or interfere with the interpretation of test results due to the administration and participation in clinical trial drugs
• •13. A person who has overreaction to clinical trial drugs, the main ingredients and components of clinical trial drugs, or other dihydropyridine-based drugs
• •14. Patients with hereditary angioedema or patients with a history of angioedema when treated with ACE inhibitors or angiotensin II receptor antagonists
• •15. Shock patients (including cardiac shock)
• •16. Pregnant or lactating women
• •17. Other persons deemed inappropriate by the tester to participate in this test