Pharmacokinetic Drug Interaction Between YH4808 and Diclofenac

December 31, 2013 updated by: Yuhan Corporation

A Randomized, Open-Label, Single-dosing and Cross-over Clinical Trial to Investigate the Safety and Pharmacokinetic Drug-Drug Interaction of YH4808 and Diclofenac in Healthy Male Volunteers

The objective of this study is to compare pharmacokinetics after single oral administration of YH4808 and Diclofenac each separately versus coadministration of YH4808 and Diclofenac in healthy male volunteers

Study Overview

Status

Status

Indicates the current recruitment status or the expanded access status.
Completed

Conditions

Conditions

The disease, disorder, syndrome, illness, or injury that is being studied. On ClinicalTrials.gov, conditions may also include other health-related issues, such as lifespan, quality of life, and health risks.

Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.

Study Type

Study Type

Describes the nature of a clinical study. Study types include interventional studies (also called clinical trials), observational studies (including patient registries), and expanded access.
Interventional

Enrollment (Actual)

Enrollment

The number of participants in a clinical study. The "anticipated" enrollment is the target number of participants that the researchers need for the study.
49

Phase

Phase

The stage of a clinical trial studying a drug or biological product, based on definitions developed by the U.S. Food and Drug Administration (FDA). The phase is based on the study's objective, the number of participants, and other characteristics. There are five phases: Early Phase 1 (formerly listed as Phase 0), Phase 1, Phase 2, Phase 3, and Phase 4. Not Applicable is used to describe trials without FDA-defined phases, including trials of devices or behavioral interventions.
  • Phase 1

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Eligibility Criteria

The key requirements that people who want to participate in a clinical study must meet or the characteristics they must have. Eligibility criteria consist of both inclusion criteria (which are required for a person to participate in the study) and exclusion criteria (which prevent a person from participating). Types of eligibility criteria include whether a study accepts healthy volunteers, has age or age group requirements, or is limited by sex.

Ages Eligible for Study

20 years to 45 years (ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Male

Description

Inclusion Criteria:

  • healthy male age 20 to 45 over 55kg with Ideal body weight(IBW)
  • No clinically important abnormal physical findings at the screening examination
  • Subject who has no congential, chronic disease and disease symptoms in medical examination result
  • Subject who is judged to be eligible by principal inverstigator or sub-investigator according to various reasons includiong ther abnorminal test results(clinical laboratory test, 12-lead GCG etc)
  • Ability to communicate well with the inverstigator and to comply with the requremetns of the entire study
  • Willingness to give written informed consent(prior to any study-related procedures beinging performed) and to be able to adhere to the study restrictions and examination schedule

Exclusion Criteria:

  • Suject who has history or presence of clinically significant diseases in liver, kidney, gastrointestinal tract, nervous system, respiratory system, endocrine system, blood tumor, cardiovascular, urinary system, and mental disorder
  • Subject who is hypersensitive to components contained in YH4808 or declofenac or related drug(ex. rebamipide, revaprazan, NSID etc)
  • Medical history of gastrointestinal disease or acid restraining surgery, gastric/ esophagus surgery(excluding appendectomy, hernia surgery)
  • Subject who has history of drug dependence or using that drug
  • Subject who had taken usual dose of any prescription durgs within 14 days before the treatment or who had used usual dose of OTC drugs within 7 days before the treatment
  • Subject who participated in antoher clinical trial within 2 monthes before enrolling in this study
  • subject who donated whole blood within 2 months or component blood within 1 month before the treatment
  • Subject who drank over 21unit/week(1 unit= 10g of alcohol) or were not able to refrain from drinking alcohol during study days
  • Subject who stopped smoking within 3 months before the treatment or detected cotinine in urine test
  • Subject with clinically significant observations considered as unsuitable based on medical judgment by the investigators

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: SUPPORTIVE_CARE
  • Allocation: RANDOMIZED
  • Interventional Model: CROSSOVER
  • Masking: NONE

Arms and Interventions

Participant Group / Arm

Participant Group / Arm

A group or subgroup of participants in a clinical trial that receives a specific intervention/treatment, or no intervention, according to the trial's protocol.
Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.
EXPERIMENTAL: YH4808 or Diclofenac or YH4808+Diclofenac(arm 1)

6 arm, 3 Sequence design

  • YH4808 or Diclofenac or YH4808+Diclofenac
  • 3 week wash out period is between each period.
Drug: YH4808
experimental drug
Drug: Diclofenac
Depain tablet 25mg
Other Names:
  • Depain tablet 25mg
Drug: YH4808+Diclofenac
EXPERIMENTAL: YH4808 or Diclofenac or YH4808+Diclofenac (arm 2)

6 arm, 3 Sequence design

  • YH4808 or Diclofenac or YH4808+Diclofenac
  • 3 week wash out period is between each period.
Drug: YH4808
experimental drug
Drug: Diclofenac
Depain tablet 25mg
Other Names:
  • Depain tablet 25mg
Drug: YH4808+Diclofenac
EXPERIMENTAL: YH4808 or Diclofenac or YH4808+Diclofenac (arm 3)

6 arm, 3 Sequence design

  • YH4808 or Diclofenac or YH4808+Diclofenac
  • 3 week wash out period is between each period.
Drug: YH4808
experimental drug
Drug: Diclofenac
Depain tablet 25mg
Other Names:
  • Depain tablet 25mg
Drug: YH4808+Diclofenac
EXPERIMENTAL: YH4808 or Diclofenac or YH4808+Diclofenac (arm 4)

6 arm, 3 Sequence design

  • YH4808 or Diclofenac or YH4808+Diclofenac
  • 3 week wash out period is between each period.
Drug: YH4808
experimental drug
Drug: Diclofenac
Depain tablet 25mg
Other Names:
  • Depain tablet 25mg
Drug: YH4808+Diclofenac
EXPERIMENTAL: YH4808 or Diclofenac or YH4808+Diclofenac (arm5)

6 arm, 3 Sequence design

  • YH4808 or Diclofenac or YH4808+Diclofenac
  • 3 week wash out period is between each period.
Drug: YH4808
experimental drug
Drug: Diclofenac
Depain tablet 25mg
Other Names:
  • Depain tablet 25mg
Drug: YH4808+Diclofenac
EXPERIMENTAL: YH4808 or Diclofenac or YH4808+Diclofenac (arm6)

6 arm, 3 Sequence design

  • YH4808 or Diclofenac or YH4808+Diclofenac
  • 3 week wash out period is between each period.
Drug: YH4808
experimental drug
Drug: Diclofenac
Depain tablet 25mg
Other Names:
  • Depain tablet 25mg
Drug: YH4808+Diclofenac

What is the study measuring?

Primary Outcome Measures

Primary Outcome Measures

In a clinical study's protocol, the planned outcome measure that is the most important for evaluating the effect of an intervention/treatment. Most clinical studies have one primary outcome measure, but some have more than one.
Outcome Measure
Time Frame
Cmax of YH4808
Time Frame: 18 points up to Day 2 or Day 3
18 points up to Day 2 or Day 3
AUClast of YH4808
Time Frame: 18 points up to Day 3
18 points up to Day 3

Secondary Outcome Measures

Secondary Outcome Measures

In a clinical study's protocol, a planned outcome measure that is not as important as the primary outcome measure for evaluating the effect of an intervention but is still of interest. Most clinical studies have more than one secondary outcome measure.
Outcome Measure
Time Frame
AUCinf of YH4808
Time Frame: 18 points up to Day 3
18 points up to Day 3
AUCinf of Diclofenac
Time Frame: 16points up to Day 2
16points up to Day 2
t1/2 of YH4808
Time Frame: 18 points up to Day 3
18 points up to Day 3
t1/2 of Diclofenac
Time Frame: 16 points up to Day 2
16 points up to Day 2
Tmax of YH4808
Time Frame: 18 points up to Day 3
18 points up to Day 3
Tmax of Diclofenac
Time Frame: 16 points up to Day 2
16 points up to Day 2
Metabolic ratio
Time Frame: 18 points up to Day 3
18 points up to Day 3

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Sponsor

The organization or person who initiates the study and who has authority and control over the study.
Yuhan Corporation

Investigators

Investigators

A researcher involved in a clinical study. Related terms include site principal investigator, site sub-investigator, study chair, study director, and study principal investigator.
  • Principal Investigator: Janghee Hong, Professor, Chungnam national university hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

Study Start

The actual date on which the first participant was enrolled in a clinical study. The "anticipated" study start date is the date that the researchers think will be the study start date.
July 1, 2013

Primary Completion (ACTUAL)

Primary Completion

The date on which the last participant in a clinical study was examined or received an intervention to collect final data for the primary outcome measure. Whether the clinical study ended according to the protocol or was terminated does not affect this date. For clinical studies with more than one primary outcome measure with different completion dates, this term refers to the date on which data collection is completed for all the primary outcome measures. The "anticipated" primary completion date is the date that the researchers think will be the primary completion date for the study.
October 1, 2013

Study Completion (ACTUAL)

Study Completion

The date on which the last participant in a clinical study was examined or received an intervention/treatment to collect final data for the primary outcome measures, secondary outcome measures, and adverse events (that is, the last participant's last visit). The "anticipated" study completion date is the date that the researchers think will be the study completion date.
December 1, 2013

Study Registration Dates

First Submitted

First Submitted

The date on which the study sponsor or investigator first submitted a study record to ClinicalTrials.gov. There is typically a delay of a few days between the first submitted date and the record's availability on ClinicalTrials.gov (the first posted date).
June 10, 2013

First Submitted That Met QC Criteria

First Submitted That Met QC Criteria

The date on which the study sponsor or investigator first submits a study record that is consistent with National Library of Medicine (NLM) quality control (QC) review criteria. The sponsor or investigator may need to revise and submit a study record one or more times before NLM's QC review criteria are met. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
June 10, 2013

First Posted (ESTIMATE)

First Posted

The date on which the study record was first available on ClinicalTrials.gov after National Library of Medicine (NLM) quality control (QC) review has concluded. There is typically a delay of a few days between the date the study sponsor or investigator submitted the study record and the first posted date.
June 12, 2013

Study Record Updates

Last Update Posted (ESTIMATE)

Last Update Posted

The most recent date on which changes to a study record were made available on ClinicalTrials.gov. There may be a delay between when the changes were submitted to ClinicalTrials.gov by the study's sponsor or investigator (the last update submitted date) and the last update posted date.
January 1, 2014

Last Update Submitted That Met QC Criteria

Last Update Submitted That Met QC Criteria

The most recent date on which the study sponsor or investigator submitted changes to a study record that are consistent with National Library of Medicine (NLM) quality control (QC) review criteria. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
December 31, 2013

Last Verified

Last Verified

The most recent date on which the study sponsor or investigator confirmed the information about a clinical study on ClinicalTrials.gov as accurate and current. If a study with a recruitment status of recruiting; not yet recruiting; or active, not recruiting has not been confirmed within the past 2 years, the study's recruitment status is shown as unknown.
December 1, 2013

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

Other Study ID Numbers

Identifiers or ID numbers other than the NCT number that are assigned to a clinical study by the study's sponsor, funders, or others. These numbers may include unique identifiers from other trial registries and National Institutes of Health grant numbers.
  • YH4808-109

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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