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Clinical Trials/NCT03787017
NCT03787017
Completed
Phase 1

A Randomized, Open-label, Single-dosing, 2X2 Crossover Study to Compare the Safety and Pharmacokinetics of FDC of MP-513 20mg and Metformin XR 1000mg With Coadministration of the Two Separate Drugs in Healthy Male Volunteers

Handok Inc.1 site in 1 country36 target enrollmentJanuary 2014

Overview

Phase
Phase 1
Intervention
FDC(MP-513 20mg/Metformin XR 1000mg)
Conditions
Healthy Volunteers
Sponsor
Handok Inc.
Enrollment
36
Locations
1
Primary Endpoint
AUC of MP-513 and metformin
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

The purpose of this study is to compare the safety and pharmacokinetic characteristics of fixed-dose combination of MP-513 20mg and Metformin XR 1000mg with coadministration of the two separate drugs in healthy male volunteers.

Detailed Description

1. Randomized, Open-label, Single-dosing, Two-treatment, Two-sequence, Two-period, crossover design 2. Wash-out period : 14days from the first dosing 3. Drug concentration analytical device : UPLC-MS/MS

Registry
clinicaltrials.gov
Start Date
January 2014
End Date
September 2014
Last Updated
7 years ago
Study Type
Interventional
Study Design
Crossover
Sex
Male

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • A healthy male adult at the age of 20 to 45 (both inclusive) at the time of screening test.
  • Body weight equal to or greater than 55 kg and calculated ideal body weight (IBW) within ±20%
  • An individual who has been given and fully understood detailed explanations about this study, decides to participate in the study of his own will, and provides written informed consent to comply with instructions.

Exclusion Criteria

  • History or presence of any clinically significant diseases in the hepatobiliary, renal, nervous(central or peripheral), respiratory, hemato-oncology, cardiovascular, urinary, musculoskeletal, immune, ear, nose and throat (ENT), mental, and, particularly, endocrine systems (e.g., diabetes mellitus, hyperlipidemia, etc.).
  • History of any gastrointestinal disease that may affect absorption of the study drug (Crohn's disease, ulcer, acute or chronic pancreatitis, etc.) or gastrointestinal surgeries (except for simple appendectomy or hernia repair).
  • Hypersensitivity to MP-513 or drugs containing metformin or other drugs in the same class as ingredients or to other drugs
  • Vital signs in a sitting position corresponding to at least one of the following criteria: systolic blood pressure ≥ 140 mmHg or \< 90 mmHg, or diastolic blood pressure ≥ 95 mmHg or \< 60mmHg.
  • Serum creatine \> upper limit of reference range
  • Required to refrain from food intake for at least 24 hours during the study period due to surgery or religious reason.
  • History or presence of drug abuse.
  • Administration of drugs that either induce or inhibit drug metabolizing enzymes, such as barbitals, within 1 month prior to the first dosing.
  • Intake of food or beverage containing grapefruit or cranberry within 1 week prior to the first dosing.
  • Administration of any ethical drugs or traditional Korean herbal medicines within 2 weeks or any over-the-counter drugs or vitamin products within 1 week prior to the first dosing

Arms & Interventions

Sequence Group A

1. 1st period : coadministration of 1 tablet of MP-513 20mg and 1 tablet of Metformin XR 1000mg, single-dose under fasted 2. 2nd period : 1 tablet of FDC(MP-513 20mg/Metformin XR 1000mg), single-dose under fasted

Intervention: FDC(MP-513 20mg/Metformin XR 1000mg)

Sequence Group A

1. 1st period : coadministration of 1 tablet of MP-513 20mg and 1 tablet of Metformin XR 1000mg, single-dose under fasted 2. 2nd period : 1 tablet of FDC(MP-513 20mg/Metformin XR 1000mg), single-dose under fasted

Intervention: MP-513 20mg

Sequence Group A

1. 1st period : coadministration of 1 tablet of MP-513 20mg and 1 tablet of Metformin XR 1000mg, single-dose under fasted 2. 2nd period : 1 tablet of FDC(MP-513 20mg/Metformin XR 1000mg), single-dose under fasted

Intervention: Metformin XR 1000mg

Sequence Group B

1. 1st period : 1 tablet of FDC(MP-513 20mg/Metformin XR 1000mg), single-dose under fasted 2. 2nd period : coadministration of 1 tablet of MP-513 20mg and 1 tablet of Metformin XR 1000mg, single-dose under fasted

Intervention: FDC(MP-513 20mg/Metformin XR 1000mg)

Sequence Group B

1. 1st period : 1 tablet of FDC(MP-513 20mg/Metformin XR 1000mg), single-dose under fasted 2. 2nd period : coadministration of 1 tablet of MP-513 20mg and 1 tablet of Metformin XR 1000mg, single-dose under fasted

Intervention: MP-513 20mg

Sequence Group B

1. 1st period : 1 tablet of FDC(MP-513 20mg/Metformin XR 1000mg), single-dose under fasted 2. 2nd period : coadministration of 1 tablet of MP-513 20mg and 1 tablet of Metformin XR 1000mg, single-dose under fasted

Intervention: Metformin XR 1000mg

Outcomes

Primary Outcomes

AUC of MP-513 and metformin

Time Frame: - 0(pre-dose), 0.25, 0.5, 1, 1.5, 2, 3, 4, 5, 6, 7, 8, 10, 12, 24, 36, 48, 72 hours post-dose(a total of 36 times, with 18 times per period)

PK assessment

Cmax of MP-513 and metformin

Time Frame: - 0(pre-dose), 0.25, 0.5, 1, 1.5, 2, 3, 4, 5, 6, 7, 8, 10, 12, 24, 36, 48, 72 hours post-dose(a total of 36 times, with 18 times per period)

PK assessment

Study Sites (1)

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