Bioequivalence Study of Deferasirox 360 mg Film-Coated Tablets Manufactured by PT. Kalbe Farma Tbk for PT. Global Onkolab Farma in Comparison with Jadenu™ 360 mg Film-Coated Tablets Manufactured by Novartis Pharma Stein AG, Stein, Switzerland.

Tahapan Penelitian : Complete
Sponsor:
Mitra Pelaksana:
PT. Pharma Metric Labs
No Registry
INA-QKA3YXR
Tanggal Input Registry : 25-03-2024

05-07-2023
Cmax, AUCt
 
Bioequivalence Study of Deferasirox 360 mg Film-Coated Tablets Manufactured by PT. Kalbe Farma Tbk for PT. Global Onkolab Farma in Comparison with Jadenu™ 360 mg Film-Coated Tablets Manufactured by Novartis Pharma Stein AG, Stein, Switzerland.
Bioequivalence Study of Deferasirox 360 mg Film-Coated Tablets Manufactured by PT. Kalbe Farma Tbk for PT. Global Onkolab Farma in Comparison with Jadenu™ 360 mg Film-Coated Tablets Manufactured by Novartis Pharma Stein AG, Stein, Switzerland.
Interventional
Deferasirox 360 mg film-coated tablets
26
 

Inclusion Criteria:

Subjects had read the subject information and signed informed consent documents, Subjects healthy male and female, Subjects age range from 18 – 55 years, Subjects’ body mass index between 18 – 25 kg/m2,Subjects had a normal electrocardiogram, Subjects had the blood pressure within normal range (systolic 90 - 120 mmHg and diastolic 60 - 80 mmHg), Subjects had the heart rate within normal range (60 – 100 bpm), Subjects had no significant disease or clinically significant abnormal laboratory values on laboratory evaluation, medical history or physical examination during screening, Subjects accepted to use protection (condom) before any intercourse with their spouse

Exclusion Criteria:

Those who were pregnant and/or nursing condition, Those with a history of contraindication or hypersensitivity to deferasirox, or other iron chelating agent, or other ingredients in the study products or a history of serious allergic reaction to any drug, a 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 surgery, renal insufficiency, hepatic dysfunction or cardiovascular disease, Those with history or presence of any coagulation disorder or clinically significant hematology abnormalities, Those with pre-existing iron deficiency (for female subjects), 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 3 months prior to the study (< 90 days), those who had donated or lost 300 ml (or more) of blood within 3 months prior to the study, Those who smoked more than 10 cigarettes a day, Those who with a history of travelling to another city within the last 14 days without following health authority regulation, Those who with a history of direct contact with a COVID-19 positive person in the subject’s neighborhood within 5 days prior to screening, Those who with a history or present of sore throat, fever (with temperature more than 37°C) or dyspnea with in the last 14 days, Those who were positive to SARS CoV-2 antigen test, Those who were positive to HIV, HBsAg, and HCV tests (to be kept confidential), Those with a 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-1241/UN2.F1/ETIK/PPM.00.02/2022
Not applicable
PPUK/PPUB number
616/STD/PML/2021
Nabila Mudin S