Microdose clinical trial for prediction of interindividual variability of PK and PD in patients administered with atorvastatin, pravastatin, rosuvastitine or telmisarta
Not Applicable
Recruiting
- Conditions
- hypertension or hyperlipidemia
- Registration Number
- JPRN-UMIN000003104
- Lead Sponsor
- APDD
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 160
Inclusion Criteria
Not provided
Exclusion Criteria
Patients wiht any conditions that the investigators judged unsuitable for the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method