Last updated: 11/03/2018 21:43:03

A Bioequivalence Study of Cefadroxil Film Coated Tablets after A Single Oral Dose Administration to Healthy Subjects

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GSK study ID
201529
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Clinicaltrials.gov ID
NCT02446496
See results summary
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Overview
Eligibility
Locations
Study documents
Results summary
Plain language summaries
Additional information

Trial overview

Official title: Comparative Randomized, Single Dose, Two-way Crossover, Open-label Study to Determine the Bioequivalence of Cefadroxil from Duricef 1 gm Film Coated Tablets (Smithkline Beecham Egypt, LLC Affiliated Co. to GalaxoSmithKline ) and Biodroxil 1 gm Film Coated tablets (Kahira Pharm &Chem .Ind. Co. for Novartis Pharma ) After a Single Oral Dose Administration of Each to Healthy Adults Under Fasting Conditions
Trial description: This is an open-label, randomized, single dose, two-sequence two-period crossover study, separated by 7 days washout interval from the first Study Drug Administration. This study is conducted to determine the bioequivalence of cefadroxil from DURICEF™ film coated tablets manufactured by Smithkline Beecham Egypt, LLC affiliated co. to GalaxoSmithKline (GSK) and cefadroxil from BIODROXIL™ film coated tablets manufactured by Kahira Pharm &Chem .Ind. Co . for Novartis Pharma (NP) after a single oral dose administration of each to healthy adult subjects under fasting conditions. In Period 1, subjects will be randomized to receive cefadroxil tablet manufactured by either GSK or NP. Following a washout of at least 7 days, subjects will be crossed over in Period 2 to receive the cefadroxil tablet that they did not receive in Period 1. DURICEF is a trademark of the GSK group of companies. BIODROXIL is a trademark of Sandoz.
Primary purpose:
Other
Trial design:
Crossover Assignment
Masking:
None (Open Label)
Allocation:
Randomized
Primary outcomes:

Maximal measured plasma concentration (Cmax) after a single dose

Timeframe: Pre-dose (0.00) and 0.25, 0.50, 0.75, 1.00, 1.25, 1.50, 1.75, 2.00, 2.50, 3.00, 4.00, 6.00, 8.00, 10.00 and 12.00 hours post-dose in each treatment period.

Area under the plasma concentration-time curve from time zero to the last measurable concentration (AUC0-t) and area under the plasma concentration-time curve from time zero to infinity (AUC0-infinity)

Timeframe: Pre-dose (0.00) and 0.25, 0.50, 0.75, 1.00, 1.25, 1.50, 1.75, 2.00, 2.50, 3.00, 4.00, 6.00, 8.00, 10.00 and 12.00 hours post-dose in each treatment period.

Secondary outcomes:

Time of the maximum plasma concentration (T-max) and Terminal half- life (T-half)

Timeframe: Pre-dose (0.00) and 0.25, 0.50, 0.75, 1.00, 1.25, 1.50, 1.75, 2.00, 2.50, 3.00, 4.00, 6.00, 8.00, 10.00 and 12.00 hours post-dose in each treatment period.

Apparent first-order elimination or terminal rate constant (Ke)

Timeframe: Pre-dose (0.00) and 0.25, 0.50, 0.75, 1.00, 1.25, 1.50, 1.75, 2.00, 2.50, 3.00, 4.00, 6.00, 8.00, 10.00 and 12.00 hours post-dose in each treatment period.

Interventions:
  • Drug: Cefadroxil tablets manufactured by GSK
  • Drug: Cefadroxil tablets manufactured by NP
    • Enrollment:
    24
    Primary completion date:
    2014-08-04
    Observational study model:
    Not applicable
    Time perspective:
    Not applicable
    Clinical publications:
    Not applicable
    Medical condition
    Infections, Urinary Tract
    Product
    cefadroxil
    Collaborators
    Not applicable
    Study date(s)
    March 2014 to April 2014
    Type
    Interventional
    Phase
    4

    Participation criteria

    Sex
    Female & Male
    Age
    18 - 55 years
    Accepts healthy volunteers
    Yes
    • Healthy male or female, age 18 to 55 years, inclusive.
    • Body weight within 15 percent of normal range according to the accepted normal values for body mass index (BMI).
    • Subjects with known allergy to the products tested.
    • Subjects whose values of BMI were outside the accepted normal ranges.
    Inclusion and exclusion criteria
    Inclusion criteria:
    • Healthy male or female, age 18 to 55 years, inclusive.
    • Body weight within 15 percent of normal range according to the accepted normal values for body mass index (BMI).
    • Medical demographics without evidence of clinically significant deviation from normal medical condition.
    • Results of clinical laboratory test are within the normal range or with a deviation that is not considered clinically significant by principal investigator.
    • Subject does not have allergy to the drugs under investigation.
    Exclusion criteria:
    • Subjects with known allergy to the products tested.
    • Subjects whose values of BMI were outside the accepted normal ranges.
    • Female subjects who were pregnant, nursing or taking birth control pills.
    • Medical demographics with evidence of clinically significant deviation from normal medical condition.
    • Results of laboratory tests which are clinically significant.
    • Acute infection within one week preceding first study drug administration.
    • History of drug or alcohol abuse.
    • 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.
    • Subject is on a special diet (for example subject is vegetarian).
    • 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.
    • 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.
    • Subject has a history of severe diseases which have direct impact on the study.
    • Participation in a bioequivalence study or in a clinical study within the last 6 weeks before first study drug administration.
    • Subject intends to be hospitalized within 6 weeks after first study drug administration.
    • Subjects who, through completion of this study, would have donated more than 500 milliliter (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.

    Trial location(s)

    Location
    Status
    Contact us
    Contact us
    Location
    GSK Investigational Site
    Cairo, Egypt
    Status
    Study Complete
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    Study documents

    Clinical study report
    Available language(s): English
    Download document(s)
    Scientific result summary
    Available language(s): English
    Download document(s)
    Protocol
    Available language(s): English
    Download document(s)

    If you wish to request for full study report, please contact - [email protected]

    Results overview

    Results posted on ClinicalTrials.gov

    Recruitment status
    Study complete
    Actual primary completion date
    2014-08-04
    Actual study completion date
    2014-08-04

    Plain language summaries

    Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.

    Additional information about the trial

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