Bioequivalence Study Of Valogrel® 75 (Clopidogrel 75 Mg) Film Coated Tablet Produced by PT IFARS Pharmaceutical Laboratories in Comparison with Plavix® 75 (Clopidogrel 75 Mg) Film Coated Tablet Manufactured by PT Aventis Pharma, Jakarta, Indonesia, Under License of Sanofi Clir Snc, France
Tahapan Penelitian : Complete
Sponsor:
PT IFARS Pharmaceutical Laboratories
Mitra Pelaksana:
PT Omega Medika Farma Laboratori
No Registry
INA-02BKQ4A
Tanggal Input Registry : 26-08-2024
| Tracking Information | |
|---|---|
| Tanggal Antisipasi Studi | 18-04-2024 |
| Outcome Primer | AUCt and Cmax |
| Outcome Skunder | AUCinf, tmax, half-life |
| Descriptive Information | |
| Judul Penelitian Popular | Bioequivalence Study Of Valogrel® 75 (Clopidogrel 75 Mg) Film Coated Tablet Produced by PT IFARS Pharmaceutical Laboratories in Comparison with Plavix® 75 (Clopidogrel 75 Mg) Film Coated Tablet Manufactured by PT Aventis Pharma, Jakarta, Indonesia, Under License of Sanofi Clir Snc, France |
| Judul Penelitian Ilmiah | Bioequivalence Study Of Valogrel® 75 (Clopidogrel 75 Mg) Film Coated Tablet Produced by PT IFARS Pharmaceutical Laboratories in Comparison with Plavix® 75 (Clopidogrel 75 Mg) Film Coated Tablet Manufactured by PT Aventis Pharma, Jakarta, Indonesia, Under License of Sanofi Clir Snc, France |
| Jenis Penelitian | Interventional |
| Intervensi | |
| Jumlah Subyek Penelitian | 38 |
| Recruitment Information | |
| Eligibility Criteria | Inclusion Criteria: Willing to sign the informed consent; Age 18 – 55 years; Body mass index between 18 – 25 kg/m2; Normotensive (systolic blood pressure 100 – 120 mmHg, diastolic blood pressure 6080 mmHg), heart rate 60 – 90 beats per minute; Healthy male (healthy criteria is determined by normal values or if outside the normal range of values but no clinically significant effects based on doctors' justification on the result of laboratory test include routine hematology, liver function, renal function, blood sugar and urinalysis; history of disease, and physical examination).Exclusion Criteria: Contraindicated and/or has history of hypersensitivity to Sitagliptin or related drug; With history or present medical condition which might significantly influence the pharmacokinetics of the study drug, e.g. chronic gastrointestinal disease, diarrhea, gastric surgery, renal insufficiency, hepatic dysfunction, or cardiovascular disease; Using any medication (prescription or non-prescription drug, food supplement, herbal medicine) within 7 days prior to the dosing day; Participated in any clinical study within 3 months prior to the study; Donated or lost 300 mL (or more) of blood within 3 months prior to the study; Smoke more than 9 sticks of cigarettes a day; Have any bleeding or coagulation disorder; Indicate the positive result on test for HbsAg, Anti-HCV, and anti-HIV; With the history of alcohol and drug abuse; If the study is conducted in Covid-19 pandemic situation, the exclusions criteria below must be applied: a. With history of direct contact with a Covid-19 positive person within last 14 days; With history or present sore throat, fever (temperature more than 37°C) or short of breath within last 14 days; Positive to Covid-19 antigen rapid test. |
| Administrative Information | |
| Nomor Persetujuan Etik | No. KET-338/ UN2.F1/ETIK/PPM.00. 02/2024 |
| Nomor Persetujuan Material Transfer Agreement | Not applicable |
| Nomor Persetujuan Pelaksanaan Uji Klinik | PPUK/PPUB number |
| Other Study ID Numbers | Protocol No. 186/FORM/OMF/2023 ver 01 ; Report No. 146/RPT/OMF/2024 ver 00 |
| Contact Person | apt. Tasha Yuliandra, M.Sc. |