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Interaction Between Omeprazole and Gliclazide in CYP2C19 Normal/ Ultrarapid Metabolisers (INTERGLIKOM)

Primary Purpose

Diabetes Mellitus, Type 2

Status
Completed
Phase
Phase 1
Locations
Bosnia and Herzegovina
Study Type
Interventional
Intervention
Omeprazole
Placebo oral tablet
Gliclazide
Sponsored by
University of Sarajevo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Diabetes Mellitus, Type 2

Eligibility Criteria

18 Years - 30 Years (Adult)MaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Men
  • Age 18-30 years
  • Non-smokers
  • CYP2C19 extensive/ultrarapid metabolisers

Exclusion Criteria:

  • medical history of hepatic, renal, gastrointestinal and hematologic disease or any acute or chronic disease, or drug allergy to sulfonylureas or PPIs or history of drug abuse
  • abnormalities in physical examination, ECG and routine clinical laboratory tests (including fasting blood glucose concentration)
  • medication use during the 14 days prior and during the study period
  • grapefruit, grapefruit juice, alcohol, beverages or food containing methylxanthines use during 72 h prior and during the study period

Sites / Locations

  • General Hospital Prim. Dr. Abdulah Nakas

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Omeprazole, Then Placebo

Placebo, Then Omeprazole

Arm Description

Healthy volunteers, CYP2C19 extensive/ultrarapid metabolisers, will receive 20 mg of omeprazole alone for 4 days, and concomitantly with single dose of gliclazide on day 5. After a wash-out period, they will receive placebo under same conditions in a cross-over manner.

Healthy volunteers, CYP2C19 extensive/ultrarapid metabolisers, will receive placebo alone for 4 days, and concomitantly with single dose of gliclazide on day 5. After a wash-out period, they will receive omeprazole under same conditions in a cross-over manner.

Outcomes

Primary Outcome Measures

Gliclazide AUC
Area under the concentration-time curve (AUC) up to the last concentration measured

Secondary Outcome Measures

Glucose
Change in glucose concentration - incremental area under the glucose concentration-time curve from 0 to 12 h
Insulin
Change in insulin concentration - incremental area under the insulin concentration-time curve from 0 to 12 h

Full Information

First Posted
December 11, 2019
Last Updated
July 19, 2021
Sponsor
University of Sarajevo
Collaborators
General Hospital Prim. Dr. Abdulah Nakas, University of Dundee, Wellcome Trust
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1. Study Identification

Unique Protocol Identification Number
NCT04198948
Brief Title
Interaction Between Omeprazole and Gliclazide in CYP2C19 Normal/ Ultrarapid Metabolisers
Acronym
INTERGLIKOM
Official Title
Interaction Between Omeprazole and Gliclazide in CYP2C19 Normal/ Ultrarapid Metabolisers
Study Type
Interventional

2. Study Status

Record Verification Date
July 2021
Overall Recruitment Status
Completed
Study Start Date
March 4, 2019 (Actual)
Primary Completion Date
August 5, 2019 (Actual)
Study Completion Date
August 5, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Sarajevo
Collaborators
General Hospital Prim. Dr. Abdulah Nakas, University of Dundee, Wellcome Trust

4. Oversight

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

5. Study Description

Brief Summary
Proton pump inhibitors (PPIs) are treatment of choice for different gastrointestinal disorders common in type 2 diabetes. Sulfonylureas (SUs) are anti-diabetes agents particularly widely used in developing countries. Gliclazide, a recommended SU drug, is metabolised in part by CYP2C19, the main enzyme responsible for the PPI metabolism. A randomised, placebo-controlled, two-sequence, two-period crossover study will be performed to explore whether gliclazide pharmacokinetics (PK) and pharmacodynamics (PD) are altered upon co-administration with omeprazole. Sixteen healthy volunteers, CYP2C19 extensive/ultrarapid metabolisers (EM/UM), will receive placebo or omeprazole alone for 4 days, and concomitantly with single dose of gliclazide on day 5. Plasma concentration of gliclazide will be measured for 24 hours, and plasma glucose and insulin levels up to 12 hours after gliclazide administration.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 2

7. Study Design

Primary Purpose
Basic Science
Study Phase
Phase 1
Interventional Study Model
Crossover Assignment
Masking
Participant
Allocation
Randomized
Enrollment
15 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Omeprazole, Then Placebo
Arm Type
Experimental
Arm Description
Healthy volunteers, CYP2C19 extensive/ultrarapid metabolisers, will receive 20 mg of omeprazole alone for 4 days, and concomitantly with single dose of gliclazide on day 5. After a wash-out period, they will receive placebo under same conditions in a cross-over manner.
Arm Title
Placebo, Then Omeprazole
Arm Type
Experimental
Arm Description
Healthy volunteers, CYP2C19 extensive/ultrarapid metabolisers, will receive placebo alone for 4 days, and concomitantly with single dose of gliclazide on day 5. After a wash-out period, they will receive omeprazole under same conditions in a cross-over manner.
Intervention Type
Drug
Intervention Name(s)
Omeprazole
Intervention Description
Omeprazole (20 mg) will be administered orally once daily for 5 days in one of the two treatment periods.
Intervention Type
Drug
Intervention Name(s)
Placebo oral tablet
Intervention Description
Placebo will be administered orally once daily for 5 days in one of the two treatment periods.
Intervention Type
Drug
Intervention Name(s)
Gliclazide
Intervention Description
Gliclazide (40 mg) will be administered orally once, concomitantly with omeprazole or placebo on day 5.
Primary Outcome Measure Information:
Title
Gliclazide AUC
Description
Area under the concentration-time curve (AUC) up to the last concentration measured
Time Frame
24 hours
Secondary Outcome Measure Information:
Title
Glucose
Description
Change in glucose concentration - incremental area under the glucose concentration-time curve from 0 to 12 h
Time Frame
12 hours
Title
Insulin
Description
Change in insulin concentration - incremental area under the insulin concentration-time curve from 0 to 12 h
Time Frame
12 hours

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
30 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Men Age 18-30 years Non-smokers CYP2C19 extensive/ultrarapid metabolisers Exclusion Criteria: medical history of hepatic, renal, gastrointestinal and hematologic disease or any acute or chronic disease, or drug allergy to sulfonylureas or PPIs or history of drug abuse abnormalities in physical examination, ECG and routine clinical laboratory tests (including fasting blood glucose concentration) medication use during the 14 days prior and during the study period grapefruit, grapefruit juice, alcohol, beverages or food containing methylxanthines use during 72 h prior and during the study period
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tanja Dujic, PhD
Organizational Affiliation
University of Sarajevo
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Aida Kulo Cesic, PhD
Organizational Affiliation
University of Sarajevo
Official's Role
Principal Investigator
Facility Information:
Facility Name
General Hospital Prim. Dr. Abdulah Nakas
City
Sarajevo
ZIP/Postal Code
71000
Country
Bosnia and Herzegovina

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Data may be shared with researchers who provide a methodologically sound proposal.
Citations:
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Interaction Between Omeprazole and Gliclazide in CYP2C19 Normal/ Ultrarapid Metabolisers

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