IDG-16177 for the Evaluation of Its Safety and Pharmacokinetics

Exclusion Criteria

• •\[Part 1 and Part 2\] Subjects/Patients who meet one or more of the following criteria will not be considered eligible to participate in Part 1 or Part 2 of the clinical study:
• •1. Subject/Patient is an employee or a family member of the Sponsor or the involved CRO.
• •2. Vulnerable subject (i.e., persons under any administrative or legal supervision or persons kept in detention).
• •3. Subject/Patient who has a positive reverse transcription polymerase chain reaction (RT PCR) test for SARS-CoV-2 prior to randomisation.
• •4. Subject/Patient who has clinical signs and symptoms consistent with SARS-CoV-2 infection; eg, fever, dry cough, dyspnea, sore throat, fatigue, or positive SARS-CoV-2 test result within 2 weeks prior to Screening.
• •5. Subject/patient who had a severe course of COVID-19 (extracorporeal membrane oxygenation, mechanically ventilated).
• •6. Recent (within previous 14 days) exposure to someone who has COVID-19 symptoms or positive test result.
• •7. Subject who has currently acute disease with active symptoms.
• •8. History of clinically significant hypersensitivity reaction to any drugs or additives.
• •9. Subjects who have a history of any gastrointestinal disease (Crohn's disease, ulcerative colitis, acute or chronic pancreatitis) or gastrointestinal surgery (excluding simple appendectomy or herniotomy) which can affect the absorption of drugs.
• •10. Subject who has participated in a clinical trial or bioequivalence test and have been administered in a product within 60 days or within 5 halflives of the drug, whichever is longer before the first study drug administration.
• •11. Subject who have taken inducer or suppressor of metabolic enzymes such as barbiturates in 30 days before the first study drug administration.
• •12. Subject who have donated whole blood in 60 days or who have donated plasma in 20 days before the first study drug administration.
• •13. Subjects who have had any prescribed medicine or herbal medicine or who have had non-prescription medicine or vitamins within 7 days or 5 half lives before the first study drug administration, whichever is longer, except for occasional intake of paracetamol. Subjects who have received a SARS-CoV-2 vaccination within 4 weeks prior to screening or plan to be vaccinated during the study.
• •14. Has a history of drug abuse or a history of alcohol abuse within 2 years prior to Screening.
• •15. Subject who do not agree to be sexually abstinent or to use a condom with spermicide when engaging in sexual activity and to not donate sperm from the first administration of study drug, during the study, and for 14 days following completion of the study (Section 5.4.4).
• •17. Has a positive test result for hepatitis B surface antigen (HBsAg) or hepatitis C virus (HCV) antibody or human immunodeficiency virus (HIV).
• •18. Has a total bilirubin \> 1.5 × ULN at Screening.
• •19. Has abnormal thyroid-stimulating hormone levels. \[Part 1\] Subjects who meet one or more of the following criteria will not be considered eligible to participate in Part 1 of the clinical study:
• •20. Subject who has abnormal vital signs, confirmed by repeat measurement at screening:
• •* systolic blood pressure (SBP) outside 90 - 139 mmHg
• •* diastolic blood pressure (DBP) outside 50 - 89 mmHg
• •* pulse rate outside 50 - 90 bpm.
• •21. Abnormal 12-lead ECG, confirmed by repeat measurement, unless considered not clinically significant by Investigator. QTcF \> 450 ms, QRS ≥ 120 ms, PR \> 220 ms at Screening.
• •22. Has an estimating glomerular filtration rate (eGFR) less than or equal to 80 mL/min using the chronic kidney disease epidemiology collaboration (CKD EPI) at Screening.
• •23. History of clinically significant gastrointestinal, renal, hepatic, neurologic, haematologic, endocrine, oncologic, pulmonary, immunologic, psychiatric, musculoskeletal, or cardiovascular disease or any other condition. \[Part 2\] Patients who meet one or more of the following criteria will not be considered eligible to participate in Part 2 of clinical study:
• •24. Has systolic blood pressure (BP) greater than 160 mm Hg or diastolic pressure greater than 100 mm Hg at Screening or baseline, confirmed by repeat measurement.
• •25. Has history of cancer. A history of basal cell carcinoma or stage 1 squamous cell carcinoma of the skin is allowed.
• •26. Has a creatine phosphokinase level ≥ 5 × upper limit of normal (ULN) at Screening.
• •27. Has alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels ≥ 2 × ULN at Screening, confirmed by repeat measurement.
• •28. Has a haemoglobin level ≤ lower limit normal (LLN) for men of the local laboratory at Screening, confirmed by repeat measurement.
• •29. The subject has a serum triglyceride level ≥ 1.5 × ULN at Screening.
• •30. Has an eGFR less than or equal to 60 mL/min using the CKD EPI at Screening.