Healthy
Conditions
Brief summary
The present study was a randomized, open-label, two-period, two-sequence, cross-over study, conducted to find out whether the etoricoxib 120 mg film-coated tablet produced by PT Dexa Medica (test drug) was bioequivalent to the reference drug (Arcoxia® Film-Coated Tablet 120 mg, PT. Schering-Plough Indonesia Tbk), under fasting condition with a fourteen days wash-out period, involving 26 healthy adult male and female subjects.
Detailed description
This was a randomized, open-label, two-period, two-sequence, cross-over study under fasting condition with a fourteen days wash-out period, involving 26 healthy adult male and female subjects. The participating subjects had an overnight fast and in the next morning were given orally either one film-coated tablet of the test drug or one film-coated tablet of the reference drug with 200 mL of water. Blood samples were drawn immediately before taking the drug (baseline), and at 15, 30, and 45 minutes and 1, 1.5, 2, 3, 4, 6, 8, 12, 18, 24, 36, 48, and 72 hours after drug administration, analysed for plasma concentrations of etoricoxib and used to evaluate the pharmacokinetics parameters of the single dose administration. After a fourteen-day washout period, the procedure was repeated using the alternate drug. The plasma concentrations of etoricoxib were determined by using a high pressure liquid chromatography with ultraviolet detection (HPLC-UV) method.
Interventions
DRUGEtoricoxib 120Mg Film-coated Tablet
One tablet of the Test drug was given orally (swallowed with 200 mL of water, without chewing), after an overnight fast, and after fasting (pre-dose) blood-sampling.
DRUGArcoxia® 120 mg Film-coated tablet (Frosst Iberica S.A., Spain for Merck Sharp & Dohme (Australia) Pty Limited, Australia, registered by PT. Schering-Plough Indonesia Tbk)
One tablet of the Reference drug was given orally (swallowed with 200 mL of water, without chewing), after an overnight fast, and after fasting (pre-dose) blood-sampling.
Sponsors
PT Equilab International
Dexa Medica Group
Study design
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
NONE
Intervention model description
This was a bioequivalence study.
Eligibility
Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
Yes
Inclusion criteria
1. Healthy male and female subjects Healthy was defined as the absence of significant disease or clinically significant abnormal laboratory values on laboratory evaluation, medical history or physical examination during screening. 2. Aged 18 - 55 years inclusive. 3. Preferably non-smokers or smoke less than 10 cigarettes per day. 4. Able to participate and would provide written informed consent to participate. 5. BMI within 18 to 25 kg/m2. 6. Vital signs (after 10 minutes rest) were within the following ranges: SBP 100 - 120 mmHg ; DBP 60 - 80 mmHg; HR 60 - 90 bpm.
Exclusion criteria
1. Personal/family history of allergy or hypersensitivity or contraindication to etoricoxib or allied drugs. 2. Pregnant or lactating women. 3. Any major illness in the past 90 days or clinically significant ongoing chronic illness 4. Presence of any clinically significant abnormal laboratory values during screening. 5. Positive Hepatitis B surface antigen (HBsAg), anti-HCV, or anti-HIV. 6. Clinically significant hematology abnormalities. 7. Clinically significant electrocardiogram (ECG) abnormalities. 8. Any surgical or medical condition (present or history) which might significantly alter the absorption, distribution, metabolism or excretion of the study drug, e.g. gastrointestinal disease including gastric or duodenal ulcers or history of gastric surgery. 9. Past history of anaphylaxis or angioedema. 10. History of drug or alcohol abuse within 12 months prior to screening for this study. 11. Participation in any clinical trial within the past 90 days calculated from the last visit. 12. History of any bleeding or coagulative disorders. 13. History of difficulty with donating blood or difficulty in accessibility of veins in left or right arm. 14. A donation or loss of 300 mL (or more) of blood within 3 months before this study's first dosing day. 15. Intake of any prescription, non-prescription drug, food supplement or herbal medicine within 14 days of this study's first dosing day.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| AUC(0-t) | 72 hours | The area under plasma concentration-time curve from time zero to last observed concentration truncated at 72-hour (AUC0-72h) |
| Cmax | 72 hours | Maximum plasma concentration |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Tmax | 72 hours | Time to maximum plasma concentration |
| T1/2 | 72 hours | The terminal half-life |
Countries
Indonesia
Outcome results
None listed