Bioequivalence Study Healthy Thai Volunteers Rosuvastatin Bioequivalence Study Healthy Thai Volunteers
Conditions
Interventions
Test (T): Generic rosuvastatin 20 mg film-coated tablet. Each tablet contains 20 mg of rosuvastatin as
rosuvastatin calcium.
,Reference (R): Rosuvastatin 20 mg film-coated tablet, CRESTOR 20 mgequival
Experimental Drug,Active Comparator Drug
Test (T): Generic rosuvastatin 20 mg film-coated tablet,Reference (R): Rosuvastatin 20 mg film-coated tablet, CRESTOR 20 mg
Sponsors
International Bio Service Co.,Ltd.
Eligibility
Sex/Gender
All
Age
18 Years to 55 Years
Inclusion criteria
Inclusion criteria: 1.Healthy Thai male or female subjects between the ages of 18 to 55 years. 2.Body mass index between 18.0 to 30.0 kg/m2. 3.Normal laboratory values, including vital signs and physical examination, for all parameters in clinical laboratory tests at screening. Any abnormalities from the normal or reference range will be carefully considered clinically relevant by the physician as individual cases, documented in study files prior to enrolling the subject in this study. 4.Non-pregnant woman (negative pregnancy test) and not currently breast feeding. 5.Female subjects abstain from either hormonal methods of contraception (including oral or transdermal contraceptives, injectable progesterone, progestin subdermal implants, progesterone-releasing IUDs, postcoital contraceptive methods) or hormone replacement therapy for at least 28 days prior to check-in in Period 1. Injectable contraceptives e.g. Depo-Provera will be discontinued at least 6 months prior to check-in in Period 1. Subjects agree to use acceptable non-hormonal contraceptive methods such as condom, diaphragm, foams, jellies, or abstinence for at least 14 days prior to check-in in Period 1 until 7 days after the end of study in Period 2. Female subjects of non-childbearing potential must meet at least one of the following criteria prior to check-in in Period 1: Postmenopausal for at least 1 year or Surgically sterile (bilateral tubal ligation, bilateral oophorectomy or hysterectomy) at least 6 months 6.Male subjects who are willing or able to use effective contraceptive e.g. condom or abstinence after check-in in Period 1 until 7 days after the end of study in Period 2. 7.Have voluntarily given written informed consent (signed and dated) by the subject prior to participating in this study.
Exclusion criteria
Exclusion criteria: 1.History of allergic reaction or hypersensitivity to rosuvastatin or to any of the excipients of the product 2.History or evidence of clinically significant renal, hepatic, gastrointestinal, hematological (anemia), endocrine (hyper-hypothyroid, diabetes), pulmonary or respiratory (asthma), cardiovascular (hyper or hypotension), psychiatric, neurologic (convulsant), allergic disease (including drug allergies, but excluding untreated, asymptomatic, seasonal allergies at time of dosing) or any significant ongoing chronic medical illness 3.History of muscular diseases myopathy, myalgia, rhabdomyolysis, muscle tenderness or weakness or hereditary muscular disorders or history of muscular toxicity with another HMG-CoA reductase inhibitor or fibrate 4.Have high risk for coronavirus infection based on risk assessment questionnaire or diagnosed as confirmed case of COVID-19 5.History about administration of first dose or second dose of COVID-19 vaccine within 30 days prior to check-in in each Period 6.History or evidence of galactose intolerance, the Lapp lactase deficiency or glucose galactose malabsorption 7.History of problems with swallowing tablet or capsule 8.History of sensitivity to heparin or heparin-induced thrombocytopenia 9.Any condition possibly affecting drug absorption gastrectomy, enterectomy, gastritis or duodenal or gastric ulceration other than appendectomy 10.History of diarrhea or vomiting within 24 hours prior to check-in in each period 11.History or evidence of drug addict or investigation with urine sample shows a positive test for drug of abuse (morphine, marijuana or methamphetamine) 12.12-lead ECG demonstrating QTc more than 450 msec, a QRS interval more than 120 msec or with an abnormality considered clinically significant at screening. If QTc exceeds 450 msec, or QRS exceeds 120 msec, the ECG will be repeated two more times and the average of the three QTc or QRS values will be used to determine the subject eligibility. 13.Investigation with blood sample shows positive test for HBsAg. 14.Abnormal liver function, more than 1.5 times of upper normal limit of reference range for ALT, AST or bilirubin levels at screening laboratory test 15.Creatine kinase levels 1.5 times of upper normal limit of reference range (unless explained by exercise) at screening laboratory test 16.Have renal creatinine clearance (CLcr) more than 30 mL per min based on serum creatinine results, using glomerular filtration rate (GFR Cockcroft-Gault formula), at the screening laboratory test 17.History or evidence of habitual use of tobacco or nicotine containing products and cannot abstain for at least 48 hours prior to check-in in Period 1 and continued for entire duration of the study 18. History or evidence of alcoholism or harmful use of alcohol (less than 2 years) alcohol consumption of more than 14 standard drinks per week for men and 7 standard drinks per week for women (A standard drink is defined as 360 mL of beer or 150 mL of wine or 45 mL of 40% distilled spirits, such as rum, whisky, brandy) 19.History or evidence of alcohol consumption or alcohol-containing products and cannot abstain for at least 48 hours prior to check-in in Period 1 and continued for entire duration of the study or alcohol breath test shows positive result 20.History or evidence of habitual consume of tea, coffee, xanthine or caffeine containing products and cannot abstain for at least 48 hours prior to check-in
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Rosuvastatin plasma concentration 0-72 hrs, 19 points, 2 ambulatory visits Cmax, AUC0-tlast and AUC0- infinity | — |
Secondary
| Measure | Time frame |
|---|---|
| Rosuvastatin Plasma Concentration 0-72 hrs, 19 points, 2 ambulatory visits Tmax, t1/2, AUC0-tlast/AUC0-infinity, AUC%extrapolate, MRT | — |
Countries
Thailand
Contacts
Public ContactUthai Suvanakoot
International Bio Service Co.,Ltd.
Outcome results
None listed