Bioequivalence study of meloxicam 15 mg tablet produced by PT Erlimpex in comparison with the comparator drug (Mobic® 15 mg Tablet produced by Boehringer Ingelheim Ellas A.E., Greece)

Tahapan Penelitian : Complete
Sponsor:
Mitra Pelaksana:
PT Equilab International
No Registry
INA-6K49QN6H
Tanggal Input Registry : 26-12-2024

02-09-2024
AUC0-t and Cmax
 
Bioequivalence study of meloxicam 15 mg tablet produced by PT Erlimpex in comparison with the comparator drug (Mobic® 15 mg Tablet produced by Boehringer Ingelheim Ellas A.E., Greece)
Bioequivalence study of meloxicam 15 mg tablet produced by PT Erlimpex in comparison with the comparator drug (Mobic® 15 mg Tablet produced by Boehringer Ingelheim Ellas A.E., Greece)
Interventional
one test drug (meloxicam 15 mg tablet produced by PT Erlimpex)
14
 

Inclusion Criteria:

1. Able to participate, communicate well with the investigators and would provide written informed consent to participate in the study; 2. Healthy male and female subjects with absence of significant disease or clinically significant abnormal laboratory values on laboratory evaluation, medical history or physical examination during screening and could be considered healthy based on the evaluation; 3. Aged 18 – 55 years inclusive; 4. Preferably non-smokers or smoke less than 10 cigarettes per day; 5. Body mass index within 18 to 25 kg/m2; 6. Vital signs (after 10 minutes rest) were within the following ranges: Systolic blood pressure : 100 – 129 mmHg Diastolic blood pressure : 60 – 84 mmHg Pulse rate : 60 – 90 bpm 7. Willing to practice abstention or non-hormonal contraception during the study.

Exclusion Criteria:

1. History of allergy or hypersensitivity or contraindication to meloxicam or allied drug. 2. Pregnant or lactating female (urinary pregnancy test will be applied to female subjects at screening and before taking the study drug). 3. Any major illness in the past 90 days or clinically significant ongoing chronic medical illness. 4. Presence of any clinically significant abnormal values during screening e.g. significant abnormality of liver function test (AST, ALT, alkaline phosphatase, total bilirubin, direct bilirubin ≥ 1.5 ULN), renal function test (serum creatinine concentration > 1.4 mg/dL and ureum ≥ 1.5 ULN), etc. 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 until this study’s first dosing day. 12. History of any bleeding or coagulative disorders. 13. Presence of difficulty in accessibility of veins in left or right arm. 14. A donation or significant blood loss within 90 days before this study’s first dosing day. 15. Intake of any prescription, non prescription drug (including hormonal contraception), food supplements or herbal medicines within 21 days of this study’s first dosing day. 16. Only complete primary COVID-19 vaccination and tested positive in COVID-19 rapid antigen test at screening and during check-in (applied during transition phase from pandemic situation).
 
No. KET-498/UN2.F1/ETIK/PPM.00.02/2024
Not applicable
PPUK/PPUB number
BE. 769/EQL/2022
Vicky Achmad Ginanjar