Bioequivalence Study of Candesartan Cilexetil 16 mg Tablet Produced by PT Trifa Raya Laboratories in Comparison with Blopress® (Candesartan Cilexetil 16 mg) Tablet Produced by PT Takeda Indonesia Licensed by Takeda Pharmaceutical Company Limited, Japan
Tahapan Penelitian : Complete
Sponsor:
PT Trifa Raya Laboratories
Mitra Pelaksana:
Not Specified
No Registry
INA-32K2CF3A
Tanggal Input Registry : 10-09-2025
| Tracking Information | |
|---|---|
| Tanggal Antisipasi Studi | 15-07-2025 |
| Outcome Primer | AUC0-t and Cmax |
| Outcome Skunder | AUC0-inf, Tmax, t½ |
| Descriptive Information | |
| Judul Penelitian Popular | Bioequivalence Study of Candesartan Cilexetil 16 mg Tablet Produced by PT Trifa Raya Laboratories in Comparison with Blopress® (Candesartan Cilexetil 16 mg) Tablet Produced by PT Takeda Indonesia Licensed by Takeda Pharmaceutical Company Limited, Japan |
| Judul Penelitian Ilmiah | Bioequivalence Study of Candesartan Cilexetil 16 mg Tablet Produced by PT Trifa Raya Laboratories in Comparison with Blopress® (Candesartan Cilexetil 16 mg) Tablet Produced by PT Takeda Indonesia Licensed by Takeda Pharmaceutical Company Limited, Japan |
| Jenis Penelitian | Interventional |
| Intervensi | Candesartan Cilexetil 16 mg Tablet Produced by PT Trifa Raya Laboratories |
| Jumlah Subyek Penelitian | 34 |
| Recruitment Information | |
| Eligibility Criteria | Inclusion Criteria: Willing to sign informed consent, healthy subjects as determined by the medical laboratory test (routine hematology, liver function, renal function, blood glucose, urinalysis), medical history, and physical examination (result that are not in normal range but clinically insignificant by medical doctor justification could be considered healthy), male or female, age between 18-55 years, normal body weight (Body Mass Index= 18-25 kg/m2), blood pressure: systolic 110-129 mmHg, diastolic 70-84 mmHg, pulse rate 60-90 bpm.Exclusion Criteria: History of allergy or hypersensitivity or contraindication to candesartan cilexetil, any major illness in the past 90 days or clinically significant ongoing chronic medical illness, history of drug or alcohol abuse, participation in any clinical trial or blood donation or significant blood loss more than 300 mL within the past 90 days prior study, positive Hepatitis B surface antigen (HBsAg), anti-HCV, or anti-HIV, pregnant or lactating female (urinary pregnancy test applied to female subjects at screening and before taking the study drug at Period I and II), any medical condition (present or history) which might affect drug kinetics e.g gastric/duodenal ulcer, history of gastric surgery, diarrhea, smoking more than 10 (ten) cigarettes per day, history of major illness, e.g. heart failure, hepatitis, hypotension, hyperglycemia, hypertension, etc., intake of any drug or food supplements less than 7 days since the start of study, significantly abnormal electrocardiogram (ECG) |
| Administrative Information | |
| Nomor Persetujuan Etik | 434/UN6.KEP/EC/2025 |
| Nomor Persetujuan Material Transfer Agreement | Not applicable |
| Nomor Persetujuan Pelaksanaan Uji Klinik | PPUK/PPUB number |
| Other Study ID Numbers | PPUB: RG.01.02.321.06.25.03656/UB |
| Contact Person | apt. Eva Sumiyarni, S.Si. |