The effect of SNR15 on urinary electrolyte and the pharmacokinetics in healthy volunteers :A randomized, double-blind, placebo-controlled crossover study
Not Applicable
- Conditions
- Healthy volunteer
- Registration Number
- JPRN-UMIN000029063
- Lead Sponsor
- TES Holdings Co.,Ltd
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
Not provided
Exclusion Criteria
1)Subjects who have allergy to medicinal and foods. 2)Subjects who has under treatment or a history of serious disease (e.g., diabetes, liver disease, kidney disease, or heart disease). 3)Subjects whose systolic blood pressure is more than 140 mmHg or diastolic blood pressure is more than 90 mmHg. 4)Subjects whose BMI is more than 30 kg/m2. 5)Subjects who make a blood donation of 400 ml within 12 weeks before the start of the intake or that of 200 ml within 4 weeks before the start of the intake. 6)Subjects who are estimated inappropriate to participate to this study by principal investigator.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method rinary electrolyte
- Secondary Outcome Measures
Name Time Method Plasma concentration of SNR15 metabolite