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PK Study of Pregabalin GLARS Tablet 150mg and IR Formulation After Multiple Dosing Under Fed Condition in Healthy Male Subjects (GLA5PR-102)

Primary Purpose

Healthy

Status
Completed
Phase
Phase 1
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Pregabalin 150mg
Pregabalin 75mg
Sponsored by
GL Pharm Tech Corporation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Healthy focused on measuring Pregabalin, GLARS

Eligibility Criteria

20 Years - 45 Years (Adult)MaleAccepts Healthy Volunteers

Inclusion Criteria:

  • 20~45 years old, Healthy Adult Male Subject
  • ≥ 50kg(Body Weight) and Ideal Body Weight ≤ ±20%

Exclusion Criteria:

  • ALT or AST > 1.25(Upper Normal Range)
  • Total Bilirubin > 1.5 (Upper Normal Range)

Sites / Locations

  • Chonbuk National University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

GLA5PR GLARS tablet 150mg(mealed)

Lyrica Capsule 75mg(mealed)

Arm Description

Pregabalin 150mg

Pregabalin 75mg

Outcomes

Primary Outcome Measures

Cmax.ss
Pharmacokinetic of Pregabalin
AUCtau
Pharmacokinetic of Pregabalin

Secondary Outcome Measures

Safety Monitoring
Adverse Event, Vital sign, Physical Exam, Laboratory Findings
Tmax
Pharmacokinetic of Pregabalin
AUC0-∞
Pharmacokinetic of Pregabalin
CL/F
Pharmacokinetic of Pregabalin
Vd/F
Pharmacokinetic parameter of Pregabalin
T1/2
Pharmacokinetic parameter of Pregabalin

Full Information

First Posted
July 9, 2012
Last Updated
November 11, 2014
Sponsor
GL Pharm Tech Corporation
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1. Study Identification

Unique Protocol Identification Number
NCT01638273
Brief Title
PK Study of Pregabalin GLARS Tablet 150mg and IR Formulation After Multiple Dosing Under Fed Condition in Healthy Male Subjects
Acronym
GLA5PR-102
Official Title
A Randomized, Open-label, Crossover Clinical Trial to Compare The Pharmacokinetics of A Pregabalin GLARS Tablet 150mg and Immediate Release Formulation After Multiple Dosing Under Fed Condition in Healthy Male Subjects
Study Type
Interventional

2. Study Status

Record Verification Date
November 2014
Overall Recruitment Status
Completed
Study Start Date
February 2014 (undefined)
Primary Completion Date
July 2014 (Actual)
Study Completion Date
November 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
GL Pharm Tech Corporation

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this clinical trial is to compare the pharmacokinetic characteristics of GLA5PR GLARS tablet 150mg and Lyrica Capsule 75mg. GLA5PR GLARS tablet 150mg is a New Formulation which is made by GL Pharm Tech. GLARS(Geometrically Long Absorption Regulated System) is New Solution to Sustained Absorption by Extending the Absorption Site. To overcome the shortcomings of the currently existing sustained release drug delivery technologies the investigators have recently developed a novel drug delivery system to enable a drug to be dissolved irrespective of the surrounding environment and further absorbed up to colon. The investigators coined this "Geometrically Long Absorption Regulated System(GLARS)".
Detailed Description
Basically, this system is a triple-layered tablet, comprised of upper and lower layers that swell and draw a sufficient amount of water, plus a highly water - soluble middle layer that rapidly draw water into the tablet core simultaneously. The water drawn into the tablet (about 3 to 4 times the weight of the tablet itself) functions as an additional media which enables additional and later drug release out of the dosage form. This serves to overcome the shortage of surrounding media that has been reported to be one of the key reasons for mal-absorption of a drug in colon. As the middle layer induces a rapid water draw into the tablet core, the penetrated water also diffuses to the upper and lower layers, which makes the tablet to rapidly swell and controls drug release. At virtually the same time, the swollen upper and lower layers form to surround a lateral side of the middle layer, which can, in turn, further control drug release. This relatively rigid swollen matrix structure makes drug release not affected by surrounding mechanical flux, which can provide relatively consistent in vivo drug release irrespective of degree of gastrointestinal motility.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Healthy
Keywords
Pregabalin, GLARS

7. Study Design

Primary Purpose
Basic Science
Study Phase
Phase 1
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
24 (Actual)

8. Arms, Groups, and Interventions

Arm Title
GLA5PR GLARS tablet 150mg(mealed)
Arm Type
Experimental
Arm Description
Pregabalin 150mg
Arm Title
Lyrica Capsule 75mg(mealed)
Arm Type
Active Comparator
Arm Description
Pregabalin 75mg
Intervention Type
Drug
Intervention Name(s)
Pregabalin 150mg
Other Intervention Name(s)
GLA5PR GLARS tablet 150mg
Intervention Description
GLA5PR GLARS tablet 150mg/day(Pregabalin 150mg once a day, after meal) for three days
Intervention Type
Drug
Intervention Name(s)
Pregabalin 75mg
Other Intervention Name(s)
Lyrica Capsule 75mg
Intervention Description
Lyrica Capsule 150mg/day(Pregabalin 75mg twice a day, after meal) for three days
Primary Outcome Measure Information:
Title
Cmax.ss
Description
Pharmacokinetic of Pregabalin
Time Frame
36hrs
Title
AUCtau
Description
Pharmacokinetic of Pregabalin
Time Frame
36hrs
Secondary Outcome Measure Information:
Title
Safety Monitoring
Description
Adverse Event, Vital sign, Physical Exam, Laboratory Findings
Time Frame
25 days
Title
Tmax
Description
Pharmacokinetic of Pregabalin
Time Frame
36hrs
Title
AUC0-∞
Description
Pharmacokinetic of Pregabalin
Time Frame
36hrs
Title
CL/F
Description
Pharmacokinetic of Pregabalin
Time Frame
36hrs
Title
Vd/F
Description
Pharmacokinetic parameter of Pregabalin
Time Frame
36hrs
Title
T1/2
Description
Pharmacokinetic parameter of Pregabalin
Time Frame
36hrs

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: 20~45 years old, Healthy Adult Male Subject ≥ 50kg(Body Weight) and Ideal Body Weight ≤ ±20% Exclusion Criteria: ALT or AST > 1.25(Upper Normal Range) Total Bilirubin > 1.5 (Upper Normal Range)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Min-Gul Kim, MD, Ph.D.
Organizational Affiliation
Chonbuk National University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Chonbuk National University Hospital
City
Jeonju-si
State/Province
Jeollabuk-do
ZIP/Postal Code
561-712
Country
Korea, Republic of

12. IPD Sharing Statement

Citations:
PubMed Identifier
30497798
Citation
Kim TE, Jeon JY, Gu N, Chang Kwon M, Kim MG. Comparative Pharmacokinetics of a Controlled-release Pregabalin Tablet (GLA5PR GLARS-NF1) and an Immediate-release Pregabalin Capsule in Healthy Male Volunteers. Clin Ther. 2018 Dec;40(12):2112-2124. doi: 10.1016/j.clinthera.2018.10.017. Epub 2018 Nov 27.
Results Reference
derived

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PK Study of Pregabalin GLARS Tablet 150mg and IR Formulation After Multiple Dosing Under Fed Condition in Healthy Male Subjects

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