Bioequivalence Study of Metformin HCl 750 mg Prolonged Release Caplets Manufactured by PT Interbat in Comparison with Glucophage® 750 mg Prolonged Release Tablets Manufactured by PT Merck Tbk, Indonesia under Licensed Merck Sante S.A.S, Lyon, France.

Tahapan Penelitian : Complete
Sponsor:
Mitra Pelaksana:
PT. Pharma Metric Labs
No Registry
INA-HL353WG
Tanggal Input Registry : 31-10-2024

17-09-2024
Cmax and AUCt
 
Bioequivalence Study of Metformin HCl 750 mg Prolonged Release Caplets Manufactured by PT Interbat in Comparison with Glucophage® 750 mg Prolonged Release Tablets Manufactured by PT Merck Tbk, Indonesia under Licensed Merck Sante S.A.S, Lyon, France.
Bioequivalence Study of Metformin HCl 750 mg Prolonged Release Caplets Manufactured by PT Interbat in Comparison with Glucophage® 750 mg Prolonged Release Tablets Manufactured by PT Merck Tbk, Indonesia under Licensed Merck Sante S.A.S, Lyon, France.
Interventional
Metformin HCl 750 mg Prolonged Release Caplets Manufactured by PT Interbat
28
 

Inclusion Criteria:

Subjects had read the subject information and were able to give written informed consent for participation in the study and comply with the study protocol/procedures, Subjects healthy male and female, Subjects’ age ranges from 18 – 55 years, Subjects’ body mass index between 18 – 25 kg/m2, Subjects had a normal electrocardiogram, Subjects had resting vital signs (after 10 – 15 minutes of resting) were within the following range : Systolic blood pressure: 90 – 129 mmHg, Diastolic blood pressure: 60 – 84 mmHg,Pulse/Heart rate: 60 – 100 beats per minute (based on ESC - ESH Guidelines for the Management of Arterial Hypertension (2018)), Subjects had no significant disease or clinically significant abnormal laboratory values on laboratory evaluation, medical history or physical examination during screening, Subjects had received the complete primary SARS CoV-2 vaccine

Exclusion Criteria:

those who were pregnant and/or nursing women those with history of contraindication or hypersensitivity to metformin, or other allied drugs, or other ingredients in the study products, or a history of serious allergic reaction to any drug, significant allergic disease, or allergic reaction those with a history or presence of medical condition which might significantly influence the pharmacokinetic of the study drug, e.g. chronic gastrointestinal disease, diarrhea, gastric /intestinal surgery, renal insufficiency, hepatic dysfunction or any cardiovascular disease those with history or presence of any coagulation disorder or clinically significant hematology abnormalities those who disagree to use non-hormonal contraceptives methods (condom) before any intercourse with their spouse within study period those who using any medication (prescription or non-prescription drug, food supplement, herbal medicine), particularly the medication known to affect the pharmacokinetics of the study drug, within one weeks prior to the drug administration day those who participated in any clinical study within the past 90 days prior to the study those who donated or losing 300 mL (or more) of blood within 3 months prior to the study those who were smoker those who had history of direct contact with a COVID-19 positive person in the subject’s neighborhood within 14 days prior to screening those who had history or present of sore throat, fever (with temperature more than 37°C), cough, cold, anosmia/loss of smell, or dyspnea within the last 14 days those who were positive to HIV, HBsAg, and HCV tests (to be kept confidential) those who had history of drug or alcohol abuse within 12 months prior to screening for this study those who were unlikely to comply with the protocol, e.g. uncooperative attitude, inability to return for follow up visits, poor venous access
 
KET-1143/UN2.F1/ETIK/PPM.00.02/2024
Not applicable
PPUK/PPUB number
829/STD/PML/2024
Nabila Mudin S