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The Effect of Naproxen on the Pharmacokinetic Profile of LC350189 in Healthy Adults

Primary Purpose

Gout, Hyperuricemia

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Xanthine Oxidase Inhibitor
nonsteroidal anti-inflammatory drug
Sponsored by
LG Chem
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Gout

Eligibility Criteria

18 Years - 50 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • The subject is male or female 18 to 50 years of age, inclusive.
  • The subject has a body mass index 18 to 32 kg/m2, inclusive, at screening.
  • The subject is judged by the investigator to be in good general health, as determined by medical history, clinical laboratory assessments, vital sign measurements, 12 lead electrocardiogram (ECG) results, and physical examination findings at screening.
  • The subject agrees to comply with all protocol requirements.
  • The subject is able to provide written informed consent.

Exclusion Criteria:

  • The subject has a medical history with any issues affecting absorption or metabolism, as judged by the investigator.
  • The subject has a positive test result for hepatitis B surface antigen, hepatitis C virus antibody, or human immunodeficiency virus types 1 or 2 antibodies at screening.
  • The subject has an estimated glomerular filtration rate (eGFR) of <90 (mL/min)/1.73 m2.
  • The subject has used any prescription (excluding hormonal birth control and hormone replacement therapy) or over the counter medications (except paracetamol [up to 2 g per day]), including herbal or nutritional supplements, within 14 days before the first dose of study drug or throughout the study.
  • The subject has consumed grapefruit or grapefruit juice, Seville orange or Seville orange containing products (eg, marmalade), or caffeine- or xanthine containing products within 48 hours before the first dose of study drug or throughout the study.
  • The subject is a smoker or has used nicotine or nicotine-containing products (eg, snuff, nicotine patch, nicotine chewing gum, mock cigarettes, or inhalers) within 6 months before the first dose of study drug.
  • The subject has a history of alcohol abuse or drug addiction within the last year or excessive alcohol consumption (regular alcohol intake >21 units per week for male subjects and >14 units of alcohol per week for female subjects) (1 unit is equal to approximately ½ pint [200 mL] of beer, 1 small glass [100 mL] of wine, or 1 measure [25 mL] of spirits).
  • The subject has a positive test result for drugs of abuse, alcohol, or cotinine (indicating active current smoking) at screening or before the first dose of study drug.

Sites / Locations

  • PPD

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Cohort

Arm Description

Period 1: LC350189 200mg (QD) Day 1~ Day 4, Period 2: Naproxen 500 mg (BID) Day 8 ~ Day 12 , Period 3 : LC350189 200mg (QD) + Naproxen 500 mg (BID) Day 13~19

Outcomes

Primary Outcome Measures

Maximun observed concentration (Cmax) of LC350189 and Naproxen from plasma
Pharmacokinetic
Area under the concentration-time curve (AUC) of LC350189 and Naproxen from plasma
Pharmacokinetic
Apparent terminal half-life (t1/2) of LC350189 and Naproxen from plasma
Pharmacokinetic

Secondary Outcome Measures

Incidence of Adverse events
Safety
Changes in concentration of uric acid in plasma by uricase method
Pharmacodynamic

Full Information

First Posted
October 21, 2019
Last Updated
June 24, 2020
Sponsor
LG Chem
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1. Study Identification

Unique Protocol Identification Number
NCT04139824
Brief Title
The Effect of Naproxen on the Pharmacokinetic Profile of LC350189 in Healthy Adults
Official Title
A Phase 1, Open-label, Fixed-sequence, 2-way Drug Interaction Study to Evaluate the Effect of Naproxen on the Pharmacokinetics of LC350189 and the Effect of LC350189 on the Pharmacokinetics of Naproxen in Healthy Subjects
Study Type
Interventional

2. Study Status

Record Verification Date
June 2020
Overall Recruitment Status
Completed
Study Start Date
January 22, 2020 (Actual)
Primary Completion Date
February 25, 2020 (Actual)
Study Completion Date
February 25, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
LG Chem

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a Phase 1, open-label, fixed-sequence, 3-period, 2-way drug interaction study designed to assess the pharmacokinetics, pharmacodynamics, safety, and tolerability of LC350189 and Naproxen when administered alone and in combination in healthy subjects.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gout, Hyperuricemia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Sequential Assignment
Masking
None (Open Label)
Enrollment
24 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Cohort
Arm Type
Experimental
Arm Description
Period 1: LC350189 200mg (QD) Day 1~ Day 4, Period 2: Naproxen 500 mg (BID) Day 8 ~ Day 12 , Period 3 : LC350189 200mg (QD) + Naproxen 500 mg (BID) Day 13~19
Intervention Type
Drug
Intervention Name(s)
Xanthine Oxidase Inhibitor
Other Intervention Name(s)
LC350189
Intervention Description
LC350189 200mg qd
Intervention Type
Drug
Intervention Name(s)
nonsteroidal anti-inflammatory drug
Other Intervention Name(s)
Naproxen
Intervention Description
Naproxen 500mg BID
Primary Outcome Measure Information:
Title
Maximun observed concentration (Cmax) of LC350189 and Naproxen from plasma
Description
Pharmacokinetic
Time Frame
From baseline up to Day 18
Title
Area under the concentration-time curve (AUC) of LC350189 and Naproxen from plasma
Description
Pharmacokinetic
Time Frame
From baseline up to Day 18
Title
Apparent terminal half-life (t1/2) of LC350189 and Naproxen from plasma
Description
Pharmacokinetic
Time Frame
From baseline up to Day 18
Secondary Outcome Measure Information:
Title
Incidence of Adverse events
Description
Safety
Time Frame
From baseline up to Day 18
Title
Changes in concentration of uric acid in plasma by uricase method
Description
Pharmacodynamic
Time Frame
From baseline up to Day 17

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: The subject is male or female 18 to 50 years of age, inclusive. The subject has a body mass index 18 to 32 kg/m2, inclusive, at screening. The subject is judged by the investigator to be in good general health, as determined by medical history, clinical laboratory assessments, vital sign measurements, 12 lead electrocardiogram (ECG) results, and physical examination findings at screening. The subject agrees to comply with all protocol requirements. The subject is able to provide written informed consent. Exclusion Criteria: The subject has a medical history with any issues affecting absorption or metabolism, as judged by the investigator. The subject has a positive test result for hepatitis B surface antigen, hepatitis C virus antibody, or human immunodeficiency virus types 1 or 2 antibodies at screening. The subject has an estimated glomerular filtration rate (eGFR) of <90 (mL/min)/1.73 m2. The subject has used any prescription (excluding hormonal birth control and hormone replacement therapy) or over the counter medications (except paracetamol [up to 2 g per day]), including herbal or nutritional supplements, within 14 days before the first dose of study drug or throughout the study. The subject has consumed grapefruit or grapefruit juice, Seville orange or Seville orange containing products (eg, marmalade), or caffeine- or xanthine containing products within 48 hours before the first dose of study drug or throughout the study. The subject is a smoker or has used nicotine or nicotine-containing products (eg, snuff, nicotine patch, nicotine chewing gum, mock cigarettes, or inhalers) within 6 months before the first dose of study drug. The subject has a history of alcohol abuse or drug addiction within the last year or excessive alcohol consumption (regular alcohol intake >21 units per week for male subjects and >14 units of alcohol per week for female subjects) (1 unit is equal to approximately ½ pint [200 mL] of beer, 1 small glass [100 mL] of wine, or 1 measure [25 mL] of spirits). The subject has a positive test result for drugs of abuse, alcohol, or cotinine (indicating active current smoking) at screening or before the first dose of study drug.
Facility Information:
Facility Name
PPD
City
Austin
State/Province
Texas
ZIP/Postal Code
78744
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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The Effect of Naproxen on the Pharmacokinetic Profile of LC350189 in Healthy Adults

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