Status:
COMPLETED
Bioequivalence Study of Dapagliflozin 10 mg Film-coated Tablets
Lead Sponsor:
Dexa Medica Group
Collaborating Sponsors:
PT Equilab International
Conditions:
Healthy
Eligibility:
All Genders
18-55 years
Phase:
NA
Brief Summary
The study was an open-label, randomized, single-dose, two-period, two-sequence, two-day crossover study, conducted to find out whether the dapagliflozin 10 mg film-coated tablet produced by PT Dexa Me...
Detailed Description
The study was an open-label, randomized, single-dose, two-period, two-sequence, two-day crossover study, conducted to find out whether the dapagliflozin 10 mg film-coated tablet produced by PT Dexa Me...
Eligibility Criteria
Inclusion
- Able to participate, communicate well with the investigators and willing to provide written informed consent to participate in the study.
- Healthy male and female subjects with absence of significant disease or clinically significant abnormal laboratory values on laboratory evaluation, medical history or physical examination during screening and could be considered healthy based on the evaluation.
- Aged 18 - 55 years inclusive.
- Preferably non-smokers or smoke less than 10 cigarettes per day.
- Body mass index within 18 to 25 kg/m2
- Vital signs (after 10 minutes rest) must be within the following ranges:
- Systolic blood pressure: 100 - 129 mmHg
- Diastolic blood pressure: 60 - 84 mmHg
- Pulse rate: 60 - 90 bpm.
- Willing to practice abstention or contraception during the study
Exclusion
- History of allergy or hypersensitivity or contraindication to dapagliflozin or allied drugs.
- Pregnant or lactating female (urinary pregnancy test was applied to female subjects at screening and before taking the study drug).
- Any major illness in the past 90 days or clinically significant ongoing chronic medical illness.
- Presence of any clinically significant abnormal values during screening e.g. significant abnormality of liver function test (AST, ALT, alkaline phosphatase, total bilirubin, direct bilirubin ≥ 1.5 ULN), renal function test (serum creatinine concentration \> 1.4 mg/dL and ureum ≥ 1.5 ULN), etc.
- Positive Hepatitis B surface antigen (HBsAg), anti-HCV, or anti-HIV.
- Positive result for COVID-19 rapid antigen test.
- Clinically significant hematology abnormalities.
- Clinically significant electrocardiogram (ECG) abnormalities.
- Any surgical or medical condition (present or history) which might significantly alter the absorption, distribution, metabolism or excretion of the study drug, e.g. gastrointestinal disease including gastric or duodenal ulcers or history of gastric surgery.
- Past history of anaphylaxis or angioedema.
- History of drug or alcohol abuse within 12 months prior to screening for this study.
- Participation in any clinical trial within the past 90 days calculated from the last visit until this study's first dosing day.
- History of any bleeding or coagulative disorders.
- Presence of difficulty in accessibility of veins in left or right arm.
- A donation or significant blood loss within 90 days before this study's first dosing day.
- Intake of any prescription (especially dapagliflozin and empagliflozin), non-prescription drug (including hormonal contraception), food supplements or herbal medicines within 21 days of this study's first dosing day.
Key Trial Info
Start Date :
March 8 2023
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 6 2023
Estimated Enrollment :
24 Patients enrolled
Trial Details
Trial ID
NCT06127212
Start Date
March 8 2023
End Date
May 6 2023
Last Update
November 13 2023
Active Locations (1)
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1
PT Equilab International
Jakarta, Indonesia, 12430