Bioequivalence Study to Compare Empagliflozin/ Metformin HCl 12.5mg/1000mg Film-coated Tablets

NCT ID: NCT06450262

Last Updated: 2024-06-10

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 36 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-01-04
• Study Completion Date: 2024-03-05

Brief Summary

Randomized, two-way, two-period, single oral dose, open-label, crossover, bioequivalence study to compare Empagliflozin/ Metformin HCl 12.5mg/1000mg film-coated tablets (12.5mg Empagliflozin / 1000mg Metformin HCl) versus Synjardy® 12.5mg/1000mg film-coated tablets (12.5mg Empagliflozin/ 1000mg Metformin HCl) in healthy subjects under fed conditions.

Conditions

Type2diabetes

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: OTHER
• Blinding Strategy: NONE

Study Groups

Empagliflozin/ Metformin HCl Film Coated Tablet

Empagliflozin/ Metformin HCl 12.5mg/1000 mg Film Coated Tablet (12.5mg Empagliflozin / 1000mg Metformin HCl)

Group Type: EXPERIMENTAL

Emapgliflozin/Metformin 12.5mg/1000mg Film-coated tablets

Intervention Type: DRUG

1 tablet of Emapgliflozin/Metformin 12.5mg/1000mg Film-coated tablets

Synjardy® film-coated tablets

Synjardy® 12.5mg/1000mg film-coated tablets (12.5mg Empagliflozin / 1000mg Metformin HCl)

Group Type: ACTIVE_COMPARATOR

Synjardy® 12.5mg/1000mg film-coated tablets

Intervention Type: DRUG

1 tablet of Emapgliflozin/Metformin 12.5mg/1000mg Film-coated tablets

Interventions

Emapgliflozin/Metformin 12.5mg/1000mg Film-coated tablets

1 tablet of Emapgliflozin/Metformin 12.5mg/1000mg Film-coated tablets

Intervention Type: DRUG

Synjardy® 12.5mg/1000mg film-coated tablets

1 tablet of Emapgliflozin/Metformin 12.5mg/1000mg Film-coated tablets

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

A. The subject is Caucasian & aged between eighteen & fifty years (18 - 50), both inclusive.

B. The subject is within the limits for his height & weight as defined by the body mass index range (18.5 - 30.0 kg/m2).

C. The subject is willing to undergo the necessary pre- & post- medical examinations set by this study.

D. The results of medical history, physical examination, vital signs & conducted medical laboratory tests are normal as determined by the clinical investigator.

E. The subject tested negative for Hepatitis B (HBsAg), Hepatitis C (HCVAb) and human immunodeficiency virus (HIVAb).

F. There is no evidence of psychiatric disorder, antagonistic personality, and poor motivation, emotional or intellectual problems likely to limit the validity of consent to participate in the study or limit the ability to comply with protocol requirements.

G. The subject is able to understand and willing to sign the informed consent form.

H. For female subjects: negative serum pregnancy test and the woman is using two reliable contraception methods and not lactating.

I. The subject has normal cardiovascular system & normal ECG recording with normal QT interval corrected for heart rate according to Bazett's formula.

J. The subject's kidney and liver (AST & ALT enzymes) function tests are within normal range. (Creatinine is accepted if below the reference range after being evaluated by the CI as clinically not significant).

K. The subject HbA1c test result is within normal range. (HbA1c is accepted if below the reference range after being evaluated by the CI as clinically not significant.) L. The subject's fasting blood glucose level is ≥ 70mg/dL before dosing.

Exclusion Criteria

A. The subject is a heavy smoker (more than 10 cigarettes per day). B. The subject has suffered an acute illness one week before dosing. C. The subject has a history of or concurrent abuse of alcohol. D. The subject has a history of or concurrent abuse of illicit drugs. E. The subject has a history of hypersensitivity and/or contraindications to the study drug and any related compounds.

F. The subject has been hospitalized within three months before the study or during the study.

G. The subject is on special diet (for example subject is vegetarian). H. The subject has consumed caffeine or xanthine containing beverages or foodstuffs within two days before dosing and until 72 hours after dosing in either study period.

I. The subject has taken a prescription medication within two weeks or even an over the counter product (OTC) within one week before dosing in each study period and any time during the study, unless otherwise judged acceptable by the clinical investigator.

J. The subject has taken grapefruit/ orange containing beverages or foodstuffs within seven (7) days before first dosing and any time during the study.

K. The subject has been participating in any clinical study (e.g. pharmacokinetics, bioavailability and bioequivalence studies) within the last 80 days prior to the present study.

L. The subject has donated blood within 80 days before first dosing. M. The subject has a history or presence of cardiovascular, pulmonary, renal, hepatic, gastrointestinal, hematological, endocrinal, immunological, dermatological, neurological, musculoskeletal or psychiatric diseases.

N. The subject has consumed drugs that may affect pharmacological or pharmacokinetic properties of Metformin or Empagliflozin (for example: Probenecid, Rifampicin, Gemfibrozil, Glimepiride, Sitagliptin, Linagliptin, Warfarin, Verapamil, Ramipril, Torasemide, Hydrochlorothiazide, Lithium, Cimetidine, Dolutegravir, Ranolazine, Trimethoprime, Vandetanib, Isavuconazole, Glucocorticoids, Insulin and insulin secretagogues (Sulphonylureas)) two weeks before dosing, during the study and two weeks after dosing.

O. Female subjects planning to become pregnant. P. The subject has a presence of ketone in urine, presence of any type of acute metabolic acidosis (such as lactic acidosis, diabetic ketoacidosis), Diabetic pre-coma and/or disease which may cause tissue hypoxia (especially acute disease, or worsening of chronic disease) such as: decompensated heart failure, respiratory failure, recent myocardial infarction and shock.

Note: Subjects, who were screened for another study and were not enrolled, might be recruited for this study provided they meet the acceptance criteria of the study.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 50 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Humanis Saglık Anonim Sirketi

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

ACDIMA Biocenter

Amman, , Jordan

Countries

Jordan

Other Identifiers

1255-2023

Identifier Type: -

Identifier Source: org_study_id