Clinical Study to Investigate the PK Profiles and Safety of CKD-385 in Healthy Volunteers Under Fed Conditions

Exclusion Criteria

• •1. 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, mpacted teeth, wisdom teeth).
• •2. 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.
• •3. 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.
• •4. Those who received investigational products or bioequivalence test drugs within 6 months before the first administration of clinical trial drugs.
• •5. Those who take drugs which may cause induction or inhibition of drug metabolism within 30 days before the first administration of investigational products.
• •6. Those who have taken any drugs that may affect the clinical trial within 10 days.
• •7. Those who donated whole blood within 2 months, or blood components within 2 week before first administration of investigational products.
• •8. Those who is unable to consume a high-fat meal provided during the study.
• •9. Those who are deemed insufficient to participate in this clinical study by investigators.