In-vivo Bioequivalence Test of Everolimus tablet (ROLIMA® 0.75 mg) with brand drugs (CERTICAN® 0.75 mg, Novartis,Switzerlan)
Not Applicable
Recruiting
- Conditions
- .
- Registration Number
- IRCT20200105046010N58
- Lead Sponsor
- anoalvand Pharmaceutical Co.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 24
Inclusion Criteria
General health
Body mass index between18-28
Informed consent
Being at the age of 18-60 years old
Exclusion Criteria
Smoking
History of cardiovascular disease
History of liver or kidney disease
Pregnancy
Alcohol & Drug addiction
History of hypersensitivity
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Determination of blood drug concentration. Timepoint: Sampling times in this study will be 0, 1, 2, 2:30, 3, 3:20, 3:40, 4, 4:20, 4: 40, 5, 6, 8, 10, 12, 24, 48, 72 hours After prescribing the tablet. Method of measurement: High Performance Liquid Chromatography tandem mass spectroscopy.
- Secondary Outcome Measures
Name Time Method