A Bioequivalence Study of Rabeprazole From Idiazole 20mg DR Tabs (GSK, Egypt) and PARIET 20 mg DR Tabs (JANSSEN, EGYPT)

NCT ID: NCT02477306

Last Updated: 2015-06-22

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 60 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2014-03-31
• Study Completion Date: 2014-03-31

Brief Summary

Comparative randomized, single dose, two-way crossover open-label study to determine the bioequivalence of Rabeprazole from Idiazole 20mg DR tabs (GSK, Egypt)and PARIET 20 mg DR tabs (JANSSEN, EGYPT) after a single oral dose administration of each to healthy adults under fasting conditions.

Detailed Description

Primary Pharmacokinetic Parameters: Cmax, AUC0→t and AUC0→∞ Secondary Pharmacokinetic Parameters: Ke, tmax and t1/2e. ANOVA using 5% significance level for transformed (with the 90% confidence intervals) and untransformed data of Cmax, AUC0→t and AUC0→∞ and for untransformed data of Ke, tmax and t1/2e. The confidence intervals of logarithmically transformed Test/Reference ratios for Cmax, AUC0→t and AUC0→∞ to be within 80.00-125.00%.

A comprehensive final report will be issued upon the completion of the study.

Conditions

Healthy

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Blinding Strategy: NONE

Study Groups

Study group

60 subjects will receive a single oral dose of idiazole 20mg DR tabs under fasting condition in one period. And the subjects will receive a single dose of PARIET 20 mg DR tabs under fasting condition in the second period. A 7 days washout interval is in between the 2 periods

Group Type: EXPERIMENTAL

Idiazole 20mg DR tabs

Intervention Type: DRUG

Delayed release tablets containing 20 mg of rabeprazole

PARIET 20 mg DR tabs

Intervention Type: DRUG

Orally administered, delayed-release, enteric-coated tablets containing 20 mg of rabeprazole sodium.

Interventions

Idiazole 20mg DR tabs

Delayed release tablets containing 20 mg of rabeprazole

Intervention Type: DRUG

PARIET 20 mg DR tabs

Orally administered, delayed-release, enteric-coated tablets containing 20 mg of rabeprazole sodium.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Healthy male or female, age 18 to 55 years, inclusive.

2. Body weight within 15% of normal range according to the accepted normal values for body mass index (BMI).

3. Medical demographics without evidence of clinically significant deviation from normal medical condition.

4. Results of clinical laboratory test are within the normal range or with a deviation that is not considered clinically significant by principal investigator.

5. Subject does not have allergy to the drugs under investigation.

Exclusion Criteria

1. Subjects with known allergy to the products tested.

2. Subjects whose values of BMI were outside the accepted normal ranges.

3. Female subjects who are pregnant, nursing or taking birth control pills.

4. Medical demographics with evidence of clinically significant deviation from normal medical condition.

5. Results of laboratory tests which are clinically significant.

6. Acute infection within one week preceding first study drug administration.

7. History of drug or alcohol abuse.

8. Subject does not agree not to take any prescription or non-prescription drugs within two weeks before first study drug administration and until the end of the study.

9. Subject is on a special diet (for example subject is vegetarian).

10. Subject does not agree not to consume any beverages or foods containing methyl-xanthenes e.g. caffeine (coffee, tea, cola, chocolate etc.) 48 hours prior to the study administration of either study period until donating the last sample in each respective period.

11. Subject does not agree not to consume any beverages or foods containing grapefruit 7 days prior to first study drug administration until the end of the study.

12. Subject has a history of severe diseases which have direct impact on the study.

13. Participation in a bioequivalence study or in a clinical study within the last 6 weeks before first study drug administration.

14. Subject intends to be hospitalized within 6 weeks after first study drug administration.

15. Subjects who, through completion of this study, would have donated more than 500 ml of blood in 7 days, or 750 ml of blood in 30 days, 1000 ml in 90 days, 1250 ml in 120 days, 1500 ml in 180 days, 2000 ml in 270 days, 2500 ml of blood in 1 year

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 55 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

GlaxoSmithKline

INDUSTRY

Sponsor Role: collaborator

Genuine Research Center, Egypt

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Ahmed Elshafeey, Ph.D. Pharma

Role: STUDY_DIRECTOR

Genuine Research Center

Locations

Genuine Research Center GRC

Cairo, , Egypt

Countries

Egypt

Related Links

http://www.pharmaweb.net/pwmirror/pw9/ifpma/ICH1.html

International conference of Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use. ICH Harmonized Tripartite Guideline Q2B. Guidelines for Validation of Analytical Procedures: Methodology. November, 1996

Other Identifiers

GRC1/14/516GSKRABFST

Identifier Type: -

Identifier Source: org_study_id