Bioequivalence Study of Sitagliptin Hydrochloride / Metformin Hydrochloride Extended-release Film Coated Tablets 50 mg /500 mg (FDC) in Healthy Adult Male and Female Subjects Under Fed Conditions.

An Oral Single-dose, Randomized, Balanced, Open-label, Two-sequence, Two-treatment, Two-period, Crossover Bioequivalence Study of Sitagliptin Hydrochloride / Metformin Hydrochloride Extended Release Film Coated Tablets 50 mg / 500 mg (FDC) of Galenicum Health S.L.U., Spain With That of JANUMET® XR (Sitagliptin Phosphate / Metformin Hydrochloride) Extended-release Coated Tablets 50 mg / 500 mg (FDC) of Merck Sharp & Dohme Pharmaceuticals Ltd., Brazilin Healthy Adult Male and Female Subjects Under Fed Conditions.

The objective of this study was to evaluate and compare the bioavailability and therefore to assess the bioequivalence of two different formulations of sitagliptin/metformin extended release tablets after a single oral dose administration under fed conditions.

Study Overview

• Status: Completed
• Conditions: Diabetes Mellitus, Type 2; Bioequivalence
• Intervention / Treatment: Drug: Sitagliptin/Metformin HCl 50/500 mg extended release film-coated tablet

• Study Type: Interventional
• Enrollment (Actual): 48
• Phase: Phase 1

Contacts and Locations

Study Locations

• Mexico
  • Nuevo León
    • San Pedro Garza Garcia, Nuevo León, Mexico, 66260
      • Avant Santé Research Center S.A. de C.V.

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult
• Accepts Healthy Volunteers: Yes

Description

Inclusion Criteria:

1. Healthy adult male and female subjects aged ≥ 18 and ≤ 55 years.
2. Subjects is a non-or ex-smoker (An ex-smoker is defined as someone who completely stopped smoking for at least 6 months before screening).
3. With a weight ≥ 50.00 kg.
4. With a body mass index (BMI) ≥ 18.5 kg/m2 and ≤ 27.0 kg/m2. This BMI range covers both COFEPRIS (18.0 to 27.0 kg/m2) and GCC (18.5 to 30.0 kg/m2) requirements.
5. Found healthy according to the clinical laboratory results and physical examination (performed within 28 days prior to the dosing on period 1).
6. Have a normal 12-lead ECG and vital signs.
7. Have laboratory test results within the laboratory's stated normal range; if not within this range, they must lack of clinical significance as judged by the PI or responsible physician.

8. If the subject of the study is female and childbearing potential / fertile (a woman is considered fertile from first menstruation and until she becomes postmenopausal, or permanently sterile), and agrees to use ANY ONE of the following forms of effective contraception / birth control (but not limited to) from the time of enrollment into the study and until at least 7 days after the last study drug administration, as judged by the PI considering the pharmacology of IP(s):

   1. Established use of oral, transdermal, injected or subdermal implanted hormonal methods.
   2. Intrauterine device (IUD or intrauterine system (IUS).
   3. Barrier methods: e.g., diaphragm, cervical cap or condom (male or female condom).
   4. Spermicidal: e.g., spermicidal foam, sponges or film.
   5. Undergone bilateral tubectomy.
   6. Accept to remain abstinent: When this is in line with the preferred and usual lifestyle of the subject. [Periodic abstinence (e.g., calendar, ovulation, symptothermal, post-ovulation methods) and withdrawal are not acceptable methods of contraception] OR Women who are postmenopausal (defined as female with no menses at least for the last 12 months without any medical cause) or permanently sterilized (e.g., undergone hysterectomy, bilateral salpingectomy or oophorectomy at least for the last 3 months).

9. If the subject of the study is male, he must be willing to use ANY ONE of the following forms of effective contraception / birth control (but not limited to) and willing not to donate sperm; from the time of enrollment into the study and until at least 7 days after the last study drug administration, as judged by the PI;

   1. Willing to remain abstinent: When this is in line with the preferred and usual lifestyle of the subject.
   2. Willing to use a male condom.
   3. Male sterilization (men who have had vasectomy, at least 3 months previous to drug administration).
10. Subject able to communicate effectively and voluntarily agreed to participate in this study by signing written informed consent after being informed sufficiently about study aspects like objectives, study procedures, characteristics of the investigational drug, expected adverse events.
11. Subject willing to adhere to protocol requirements as evidenced by signing the informed consent form approved by the REC & RC.

Exclusion Criteria:

1. Have any history of allergy or hypersensitivity to sitagliptin and metformin or to any of its metabolites/derivatives or related drugs or excipients.
2. Have a positive test result for HBs Ag or HCV Ab or HIV antibodies (types 1 and 2) or VDRL.
3. The study drug is contraindicated for medical reasons for the subject.
4. Have any history or presence of clinically significant cardiovascular, pulmonary, hepatic, renal, gastrointestinal, hematological, neurological or psychiatric disease or disorder (e.g., subjects with uncontrolled hypertension, phaeochromocytoma, carcinoid, thyrotoxicosis, bipolar depression, schizoaffective disorder and acute confusional states) as judged by the PI considering the pharmacology of IP(s).

5. Presence of gastrointestinal, hepatic or kidney disease, or surgery or any other condition known to interfere with the absorption, distribution, metabolism or excretion of drugs or known to potentiate or predispose to undesired effects.

   Or Subjects with a history of gastrointestinal disorder or surgery which may affect the absorption of investigational drug.

6. Have history or presence of Corona Virus Disease (COVID-19) during the last 30 days prior to dosing of period 1.

   Or Have history of vaccination (any dose) for COVID-19 during the last 14 days prior to dosing of period 1.

   Or Any planned vaccination for COVID-19 during the study period.

7. Have history or presence of cancer.
8. Have a history or evidence of drug abuse or alcohol abuse.
9. Have a history of smoking cigarettes during the last 6 months prior to screening.
10. Have any history of gastrointestinal ulcers / bleeding.
11. Have difficulty in swallowing solid medications such as tablet.
12. Have a history or evidence of difficulty with donating blood.
13. Have clinically significant abnormal laboratory tests results.
14. Have a systolic blood pressure < 90 or > 140 mmHg or diastolic blood pressure is < 60 or > 90 mmHg
15. Have a pulse rate less than 60 bpm or greater than 100 bpm (lower range will be accepted up to 45 bpm in case of athlete).
16. Have used any prescribed medication during the last 14 days preceding the first dosing, or use OTC, herbal products during the last 7 days or use medicinal enzyme inhibitors / inducers during 30 days preceding the first dosing.
17. Have participated in a drug research study the last 3 months or donated blood within the last 3 months.
18. Have a positive result for the alcohol test (breath / saliva) or drugs of abuse test [Cannabinoids (Marijuana/Tetrahydrocannabinol-THC), Cocaine, Opiates/Morphine, Amphetamine, Methamphetamine and Benzodiazepines] performed during screening.
19. Female subject, who is currently breast feeding or a who is pregnant or who is likely to become pregnant during the study.
20. Female subject has a positive pregnancy test result.
21. Unwillingness or inability to comply with the instructions on the restrictions and/or study procedures described in this Protocol.
22. If the PI considers, for any reason, that the volunteer is not a suitable candidate to receive the study drug.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Other
• Allocation: Randomized
• Interventional Model: Crossover Assignment
• Masking: None (Open Label)

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Reference group; After an overnight fasting of at least 10.00 hours prior to start of high-fat and high-calorie (approximately 800 to 1000 calories) breakfast, subjects were administered a single-dose of the reference product along with 250 mL of 20% glucose in water solution at room temperature.	Drug: Sitagliptin/Metformin HCl 50/500 mg extended release film-coated tablet; The subjects randomly received single oral dose of Sitagliptin/Metformin HCl 50/500 mg extended release film-coated tablet (Test or reference)
Experimental: Test group; After an overnight fasting of at least 10.00 hours prior to start of high-fat and high-calorie (approximately 800 to 1000 calories) breakfast, subjects were administered a single-dose of the test product along with 250 mL of 20% glucose in water solution at room temperature.	Drug: Sitagliptin/Metformin HCl 50/500 mg extended release film-coated tablet; The subjects randomly received single oral dose of Sitagliptin/Metformin HCl 50/500 mg extended release film-coated tablet (Test or reference)

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Peak Plasma Concentration (Cmax)	Evaluation of Peak Plasma Concentration (Cmax)	48 hours
Area under the plasma concentration versus time curve (AUC) 0-t	Evaluation of Area Under Plasma Concentration-Time Curve from Time Zero to the Last Measurable Concentration	48 hours
Area under the plasma concentration versus time curve (AUC) 0-inf (Metformin only)	Area Under Plasma Concentration-Time Curve from Time 0 to Infinite	48 hours

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Number of participants with adverse events (AEs)	To evaluate the safety and tolerability of a single oral dose of Sitagliptin /Metformin extended-release film coated tablets 50 mg /500 mg (FDC) under fed conditions	1 week

Collaborators and Investigators

• Sponsor: Galenicum Health

Study record dates

Study Major Dates

• Study Start (Actual): January 16, 2023
• Primary Completion (Actual): February 13, 2023
• Study Completion (Actual): February 13, 2023

Study Registration Dates

• First Submitted: November 2, 2023
• First Submitted That Met QC Criteria: November 8, 2023
• First Posted (Estimated): November 9, 2023

Study Record Updates

• Last Update Posted (Estimated): November 9, 2023
• Last Update Submitted That Met QC Criteria: November 8, 2023
• Last Verified: November 1, 2023

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Glucose Metabolism Disorders; Metabolic Diseases; Endocrine System Diseases; Diabetes Mellitus; Diabetes Mellitus, Type 2; Hypoglycemic Agents; Physiological Effects of Drugs; Molecular Mechanisms of Pharmacological Action; Enzyme Inhibitors; Hormones; Hormones, Hormone Substitutes, and Hormone Antagonists; Protease Inhibitors; Incretins; Dipeptidyl-Peptidase IV Inhibitors; Metformin; Sitagliptin Phosphate
• Other Study ID Numbers: AS/CJ/ABR-22/0014

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No