A Phase I Study of TRN501 in Healthy Volunteers

Prior treatment

• A lifetime history of suicide attempts (including ongoing, previously interrupted or aborted attempts) or suicidal ideation within 6 months prior to screening. Assess using the C-SSRS. If there is a history of suicidal ideation, the timing of the ideation should be confirmed.
  • Those with abnormal resting blood pressure and pulse rate (any of the following) at screening.
  • Supine systolic blood pressure 140 mmHg or above or less than 90 mmHg
  • Supine diastolic blood pressure 90 mmHg or above or less than 50 mmHg
  • Supine pulse rate of less than 40 beats per minute or more than 100 beats per minute
  • Systolic blood pressure in the standing position (after 3 minutes in the standing position) is 20 mmHg or more lower than in the supine position, or symptoms such as dizziness are present.
• Persons with previous resection of the upper gastrointestinal tract (esophagus, stomach, duodenum, upper small intestine) (excluding appendicectomy).
• Persons who have taken drugs (prescription drugs, over-the-counter drugs, herbal medicines, dietary supplements, vitamins, etc.) within one week prior to admission (or 5 times the half-life, whichever is longer), or who will be required to take such drugs by the end of the examination.
• Smokers, or those who have quit smoking within 6 months prior to admission.
• Those who have collected 400 mL or more of blood within 12 weeks prior to admission or 200 mL or more of blood within 4 weeks through blood donation, etc.
• Who received all other unapproved drugs (including investigational drugs, drugs administered through clinical research, unapproved combination drugs, and new dosage forms) within 3 months (or 5 times the half-life, whichever is longer) prior to the administration of the investigational drug. However, even if the period is longer than this, those who have been judged by the investigator to be inappropriate to participate in this study in consideration of the characteristics of the previous study drug.

Other illness

• Persons with disease or findings that are judged to affect this clinical study from the viewpoint of safety and/or evaluation.
• Persons with mental, central nervous system, cardiopulmonary, hepatic, renal, hematological, metabolic, or other diseases that may affect this study.
• Persons with hypersensitivity or allergy to the active ingredients or additives of TRN501 or persons with a history of severe allergies (anaphylaxis, etc.) due to other drugs.
• Persons with chronic abnormal bowel movements (chronic constipation, chronic diarrhea, irritable bowel syndrome, etc.).
• Persons with a history of drug abuse or alcohol dependence, or complications.
• Those who are positive for either syphilis seroreaction, HBs (hepatitis B) antigen, HCV (hepatitis C virus) antibody, or HIV antigen/antibody at the time of screening.

Lab values

• Those with hemoglobin level less than 13.0 g/dL at screening.

Other

• Others who have abnormal findings in blood or urine tests and who are judged by the investigator to be unsuitable as participants for this study.
• Those who have abnormalities in the electrocardiogram at the time of screening and who are judged by the investigator to be unsuitable as participants for this study.
• Others who are judged by the investigator to be unsuitable as participants for this study.

• The person who has been fully informed of the purpose and details of this clinical study prior to the start of screening and who has given his written consent to participate in this clinical study of his own free will.
• Japanese healthy adult male volunteers between the ages of 18 and 45 on the date of obtaining written consent.
• Those whose weight at the time of screening is 50 kg or more and Body Mass Index (BMI) between 18.5 kg/m\^2 and 25.0 kg/m\^2.
• Those who have been diagnosed as healthy by the investigator in charge of the screening test and are deemed to be eligible for this study.
• For participants who have a fertile partner or a pregnant female partner, those who agree to dual contraception by combining vasectomy or condom use for the male participant and another contraceptive method for the female partner (tubal ligation, intrauterine contraceptive device, or oral contraceptive) from the date of signing the informed consent form until the end of the study.