Bioavailability Study of Ondansetron Orally Disintegrating Tablets Under Fed Conditions

Overview

To compare the single-dose bioavailability of Ondansetron ODT 8 mg and Zofran 8 mg

Full Title of Study: “Comparative, Randomized, Single-Dose, Cross Over Bioavailability Study of Kali’s Ondansetron ODT 8 mg With That of GlaxoSmithKine’s Zofran ODT 8 mg in Healthy Adult Subjects Under Fed Conditions”

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: Randomized
    • Intervention Model: Crossover Assignment
    • Masking: None (Open Label)
  • Study Primary Completion Date: September 2002

Detailed Description

To compare the single-dose bioavailability of Kali's Ondansetron ODt 8 mg with that of GlaxoSmithKine's Zofran 8 mg under fed conditions

Interventions

  • Drug: Ondansetron
    • ODT, 8 mg, single-dose, fed conditions
  • Drug: Zofran
    • ODT, 8 mg, single-dose, under fed conditions

Arms, Groups and Cohorts

  • Experimental: A
    • Subjects received Kali formulated products under fed conditions
  • Active Comparator: B
    • Subjects received GlaxoSmithKline’s formulated products under fed conditions

Clinical Trial Outcome Measures

Primary Measures

  • Rate and Extend of Absorption
    • Time Frame: 24 Hours

Participating in This Clinical Trial

Inclusion Criteria

  • Subjects meeting all of the following criteria may be included in the study – Availability of subject for the entire study period and willingness to adhere to protocol requirements as evidenced by the informed consent from duly signed by the subject. – Males and females aged from 18 to 50 years with a body mass index (BMI) within 19-30; demographic data (sex, age, ethnic group, body weight, height and smoking habits) will be recorded and reported in the final report. – Clinical laboratory values within the laboratory's stated normal range; if not within this range, they must be without ant clinical significance and must be recorded as such in the CRF ( laboratory tests are presented in section 7.1.3) – Healthy according to the laboratory results and physical examination. – Normal cardiovascular function according to the to ECG. – Non or ex-smokers. Exclusion Criteria:

  • Significant history of hypersensitivity to ondansetron or any related products as well as severe hypersensitivity reactions (like angioedema) to any drugs. – Presence or history of significant gastrointestinal, liver or kidney disease, or any other conditions known to interfere with the absorption, distribution, metabolism or excretion of drugs or known to potentiate or predispose to undesired effects. – Presence or history of significant cardiovascular, pulmonary, hematologic, neurologic, psychiatric, endocrine, immunologic or dermatologic disease. – Females who pregnant, lactating or are likely to become pregnant during the study phases. – Females or childbearing potential who refuse to use an acceptable contraceptive regimen throughout the study. – Positive pregnancy test before and during the study. – Maintenance therapy with any drug, or significant history of drug dependency, alcohol abuse (>3 units of alcohol per day, intake of excessive alcohol, acute or chronic), or serious psychological disease. – Any clinically significant illness in the previous 28 days before day 1 of this study. – Use of enzyme-modifying drugs in the previous 28 days before day 1 of this study (all barbiturates, corticosteroids, phenylhydantoins, etc.) – Participation in another clinical trial in the previous 28 days before day 1 of this study. – Donation of 500 mL of blood (Canadian Blood Services, Hema-Quebec, clinical studies, etc.) in the previous 56 days before day 1 of this study. – Positive urine screenings of drugs of abuse (drug names are presented in section 7.1.4). – Positive results to HIV, HBsAg or anti-HCV tests. – History of fainting upon blood sampling.

Gender Eligibility: All

Minimum Age: 18 Years

Maximum Age: 50 Years

Are Healthy Volunteers Accepted: Accepts Healthy Volunteers

Investigator Details

  • Lead Sponsor
    • Par Pharmaceutical, Inc.
  • Collaborator
    • Algorithme Pharma Inc
  • Provider of Information About this Clinical Study
    • Dr.Alfred Elvin/ Diector Biopharmaceutics, Par Pharmaceutical, Inc.
  • Overall Official(s)
    • Christian Aumais, Principal Investigator, Algotithme Pharma Inc

Clinical trials entries are delivered from the US National Institutes of Health and are not reviewed separately by this site. Please see the identifier information above for retrieving further details from the government database.

At TrialBulletin.com, we keep tabs on over 200,000 clinical trials in the US and abroad, using medical data supplied directly by the US National Institutes of Health. Please see the About and Contact page for details.