Bioequivalence study of Fordiamin XR (Metformin Hydrochloride 500 mg) prolonged release tablet produced by PT Konimex in comparison with Glucophage® XR (Metformin Hydrochloride 500 mg) prolonged release tablet manufactured by PT Merck Tbk, Jakarta, Indonesia, under licence from Merck Sante Sas, France.
Tahapan Penelitian : Complete
Sponsor:
PT Konimex
Mitra Pelaksana:
PT Omega Medika Farma Laboratori
No Registry
INA-2K190RWD
Tanggal Input Registry : 18-09-2025
| Tracking Information | |
|---|---|
| Tanggal Antisipasi Studi | 06-01-2025 |
| Outcome Primer | AUCt and Cmax |
| Outcome Skunder | AUCinf, tmax, half-life |
| Descriptive Information | |
| Judul Penelitian Popular | Bioequivalence study of Fordiamin XR (Metformin Hydrochloride 500 mg) prolonged release tablet produced by PT Konimex in comparison with Glucophage® XR (Metformin Hydrochloride 500 mg) prolonged release tablet manufactured by PT Merck Tbk, Jakarta, Indonesia, under licence from Merck Sante Sas, France. |
| Judul Penelitian Ilmiah | Bioequivalence study of Fordiamin XR (Metformin Hydrochloride 500 mg) prolonged release tablet produced by PT Konimex in comparison with Glucophage® XR (Metformin Hydrochloride 500 mg) prolonged release tablet manufactured by PT Merck Tbk, Jakarta, Indonesia, under licence from Merck Sante Sas, France. |
| Jenis Penelitian | Interventional |
| Intervensi | Not Specified |
| Jumlah Subyek Penelitian | 28 |
| 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 – 100 beats per minute (as assessed through both pulse examination and ECG test results), respiration rate 12-20 x/minutes, body temperature < 37.3°C; Healthy male/female (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 Sildenafil 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; Show abnormal result or not within the acceptance range (clinically significant effect based on doctor’s justification) in the electrocardiography (ECG) test result; Using any medication (prescription or non-prescription drug, food supplement, herbal medicine) within 7 days prior to the study; 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 dosing day; Smoke more than 9 sticks of cigarettes a day; Have any bleeding or coagulation disorder; With the history of alcohol and drug abuse; Indicate the positive result on test for HbsAg, Anti-HCV, and anti-HIV; pregnant or lactating female (urinary pregnancy test applied to female subject at screening and before taking the study drug); |
| Administrative Information | |
| Nomor Persetujuan Etik | No. KET-1655/ 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. 218/FORM/OMF/2024 ver 02 Report No. 168/RPT/OMF/2025 ver 00 |
| Contact Person | apt. Kireyne E SItanggang, S.Farm |