Healthy adult subjects
Conditions
Interventions
Single oral dose of SK-1887 or placebo with dose escalation
Sponsors
Kazuo Kuyama
Eligibility
Sex/Gender
Male
Inclusion criteria
Inclusion criteria: 1. Subjects aged 18 years or older but less than 40 years (at the time of informed consent) 2. Subjects with a body weight of 50 kg or more but less than 80 kg (at the time of screening) 3. Subjects with BMI (weight (kg)/[height (m)]2) of 18.5 to less than 25.0 (at the time of screening) 4. Subjects with SBP of under 120 mmHg and DBP of under 80 mmHg (at the time of screening) 5. Subjects who have the capacity to consent and provide written consent.
Exclusion criteria
Exclusion criteria: 1. Subjects with current medical history. 2. Subjects with a past medical history of endocrine, neoplastic, ocular, urologic, hepatic, renal, cardiovascular, hematologic, gastrointestinal, respiratory, psychiatric/cranial nerve, or infectious disease that the investigator or sub-investigator considers to affect the safety of the subject and the evaluation of the investigational drug 3. Subjects with a pulse rate of less than 50 beats/minute at the time of screening test 4. Subjects with clinically significant abnormalities in the resting 12-lead electrocardiogram of the screening test 5. Subjects with current or previous drug depencence, alcohol dependence, hypersensitivity or/and food allergy. 6. Subjects who consume an average of 20 g or more of alcohol per day. 7. Subjects who smoked within 28 days prior to admission 8. Subjects who used any drugs or supplements within 14 days prior to admission. 9. Subjects who are considered by the investigator or subinvestigator to be inappropriate to participate in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Safety, pharmacokinetics, pharmacodynamics , dietary effects | — |
Contacts
Public ContactKuyama Kazuo
Sanwa Kagaku Kenkyusho Co.,Ltd.
Outcome results
None listed