Clinical Research Directory

Inclusion Criteria: * Healthy adults aged 19 years or older at the time of screening. * Body mass index (BMI) between 18 and 30 kg/m². * Male subjects: body weight ≥ 50 kg. * Female subjects: body weight ≥ 45 kg. * Clinically healthy based on medical history, physical examination, vital signs, electrocardiogram (ECG), and laboratory test results, as determined by the investigator. * Willing and able to provide written informed consent after receiving a full explanation of the study. * Subjects (and their partners, if applicable) agree to use highly effective, non-hormonal contraception from the first dosing day until one week after the last dose. Exclusion Criteria: * Use of drugs known to induce or inhibit drug-metabolizing enzymes within 30 days prior to the first dose, or any medication likely to interfere with the study within 10 days prior to dosing. * Participation in any clinical trial involving investigational products within 6 months prior to the first dose. * Whole blood donation within 8 weeks, or component blood donation within 2 weeks prior to the first dose. * History of gastrointestinal surgery that may affect drug absorption (excluding appendectomy and hernia repair). * Known hypersensitivity to the investigational product or its components. * Known metabolic or genetic disorders such as galactose intolerance, lactase deficiency, glucose-galactose malabsorption, or phenylketonuria. * History of clinically significant psychiatric illness. * Pregnant or breastfeeding women, or women with a possibility of pregnancy.