Empagliflozin 10 mg Tablets Relative to Jardiance 10 mg

Healthy Subjects Clinical Trial

Official title: A Bioequivalence Study of Empagliflozin 10 mg Tablets Relative to Jardiance 10 mg, in Healthy Thai Volunteers Under Fasting Condition

Status Not yet recruiting

Clinical Trial Summary

The study is to compare the rate and extent of absorption of a generic formulation with that of a reference for mulation when given as equal labeled dose. The study will be randomized, open-label, single dose, two way crossover design with two-period, two-treatment and two-sequence under fasting condition and at least 7 days washout period between the doses.

Clinical Trial Description

Title A Bioequivalence study of a randomized, open-label, single dose, two-way crossover design with two-period, two-treatment and two-sequence of Empagliflozin 10 mg tablets relative to Jardiance 10 mg, in healthy Thai volunteers under fasting condition

Objectives The primary objective is to compare the rate and extent of absorption of a generic formulation with that of a reference formulation when given as equal labeled dose. The secondary objective is to evaluate the safety after oral administration of both test and reference formulation in healthy Thai volunteers under fasting condition.

Study Design Randomized, open-label, single dose, two-way crossover design with two-period, two-treatment and two-sequence under fasting condition and at least 7 days washout period between the doses.

Sample Size 26 Healthy Human Thai subjects. Two extra subjects, if available, may be checked-in on the day of check in of period-I to compensate for any dropout prior to dosing of period-I. These subjects will be dosed if there are dropouts prior to dosing in period-I. If there are no dropouts, these subjects will be checked-out without being dosed after completion of dosing in period-I.

Drug-Product Test-Product: Empagliflozin 10 mg tablets Reference-product: Jardiance 10 mg (Empagliflozin 10 mg tablets) Manufactured by: ROTTENDORF PHARMA GMBH, Germany

Administration After an overnight fasting at clinical facility of at least 10 hours, each volunteer will receive a single dose of Empagliflozin 10 mg tablets of either test or reference with 240 mL of 20% glucose solution in water. Each volunteer will be allowed to drink water as desired except 1 hour before and after drug administration. The formulation is given in a crossover fashion as per the randomization schedule. After the administration, the subject's oral cavity will be checked by using flashlight to confirm complete medication and fluid consumption by pharmacist.

Blood Schedule In each period, a total of 19 blood samples (approximately 7 mL each) will be collected pre-dose (0.00 hour) and at 0.25, 0.50, 0.75, 1.00, 1.25, 1.50, 1.75, 2.00, 2.50, 3.00, 4.00, 6.00, 8.00, 10.00, 12.00, 24.00, 36.00 and 48.00 hours after study drug administration, respectively. The sample collection at 36.00 and 48.00 hours after dosing will be on ambulatory basis (i.e., on separate visit.).

Sample Collection Blood samples will be collected through an indwelling catheter placed in a vein using disposable syringe or through fresh venipuncture with disposable syringes and needles. Approximately 7 mL blood sample will be withdrawn and transferred to sample collection pre-labeled tubes containing K3EDTA as anticoagulant at each sampling time point. After collection of blood samples from each subject at each time point, samples will be centrifuged at 4000 rpm for 5 minutes at 4±2°C. After centrifugation, the plasma samples will be aliquoted into two pre-labeled cryovials for approximately 1 mL per cryovial. Cryovials containing plasma sample will be stored at -70±10 °C until analysis.

Analytical Method Empagliflozin plasma concentration will be assayed as per international Guidelines/In-house SOP by using a UPLC-MS/MS method.

Pharmacokinetic Parameters Primary pharmacokinetic parameters: Cmax, AUC0→t and AUC0→∞

Secondary pharmacokinetic parameters: Tmax, T1/2, Kel, AUC0→t/AUC0→∞ will be determined from the plasma concentration data of analytes.

Statistical Analysis ANOVA, two one-sided tests for bioequivalence, for log-transformed pharmacokinetic parameters Cmax, AUC0→t and AUC0→∞ will be performed.

Acceptance Criteria for Bioequivalence To be considered as bioequivalent, the 90% CI of Cmax, AUC0→t and AUC0→∞ of Empagliflozin of test and reference products should be in the interval of 80.00-125.00% for the log-transformed data. ;

Related Conditions & MeSH terms

• Healthy Subjects

• NCT number: NCT06232239
• Study type: Interventional
• Source: Bio-innova Co., Ltd
• Contact: Sasitorn Kittivoravitkul, Ph.D.
• Phone: 022549008
• Email: sasitorn_k@bio-innova.com
• Status: Not yet recruiting
• Phase: Phase 1
• Start date: February 27, 2024
• Completion date: April 19, 2024