Bioequivalence Study of Zycin® 500 mg Film-Coated Caplets Manufactured by PT Interbat in Comparison with Zithromax® 500 mg Film-Coated Tablets Manufactured by PT Pfizer Indonesia Under Supervision from Pfizer Inc., New York, NY., USA

Tahapan Penelitian : Complete
Sponsor:
Mitra Pelaksana:
PT Pharma Metric Labs
No Registry
INA-007774Z
Tanggal Input Registry : 26-09-2024

13-08-2024
Cmax and AUCt
 
Bioequivalence Study of Zycin® 500 mg Film-Coated Caplets Manufactured by PT Interbat in Comparison with Zithromax® 500 mg Film-Coated Tablets Manufactured by PT Pfizer Indonesia Under Supervision from Pfizer Inc., New York, NY., USA
Bioequivalence Study of Zycin® 500 mg Film-Coated Caplets Manufactured by PT Interbat in Comparison with Zithromax® 500 mg Film-Coated Tablets Manufactured by PT Pfizer Indonesia Under Supervision from Pfizer Inc., New York, NY., USA
Interventional
Zycin® 500 mg Film-Coated Caplets
34
 

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 were 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 ranges:Systolic blood pressure: 90 – 129 mmHg, Diastolic blood pressure: 60 – 84 mmHg, Pulse/Heart rate: 60 – 100 beats per minutes, 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 condition, those with a history of hypersensitivity or contraindication to azithromycin, or 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 pharmacokinetics of the study drug, e.g. chronic gastrointestinal disease, diarrhea, gastric/intestine surgery, renal insufficiency, hepatic dysfunction or any cardiovascular disease, those who had history or presence of any coagulation disorder or clinically significant hematology abnormalities, those who disagreed to use non-hormonal contraceptives methods (condom) before any intercourse with their spouse within study period, those who were using any medication (prescription or non-prescription drug, food supplement, herbal medicine), particularly the medication known to affect the pharmacokinetic of the study drug, within one week prior to the drug administration day, those who had participated in any clinical study within the past 90 days prior to the study, those who had donated or lost 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 the last 14 days prior to screening those with a history or present of sore throat, fever (with temperature more than 37°C), cough, cold, anosmia/loss of smell, or dyspnea with in the last 14 days, those who were positive result for HIV, HbsAg, and HCV tests (to be kept confidential), those were 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-963/UN2.F1/ETIK/PPM.00.02/2024
Not applicable
PPUK/PPUB number
831/STD/PML/2024
Nabila Mudin S