Bioequivalence Study of Citalopram Hydrobromide Tablets 40 mg of Dr.Reddy's Laboratories Limited Under Fed Conditions

This study has been completed.
Sponsor:
Information provided by:
Dr. Reddy's Laboratories Limited
ClinicalTrials.gov Identifier:
NCT01149980
First received: June 21, 2010
Last updated: June 23, 2010
Last verified: June 2010
  Purpose

This is a bioequivalence study of Citalopram Hydrobromide Tablets 40 mg of Dr.Reddy's Laboratories Limited under fed conditions.


Condition Intervention Phase
Healthy
Drug: Citalopram Hydrobromide
Phase 1

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Bio-equivalence Study
Intervention Model: Crossover Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Randomized, 2-way Crossover, Bioequivalence Study of Citalopram Hydrobromide 40 mg Tablets and Celexa 40 mg Tablets Administered as 1 x 40 mg Tablet in Healthy Subjects Under Fed Conditions

Resource links provided by NLM:


Further study details as provided by Dr. Reddy's Laboratories Limited:

Primary Outcome Measures:
  • Bioequivalence based on Cmax and AUC parameters [ Time Frame: 2 Months ] [ Designated as safety issue: No ]

Enrollment: 24
Study Start Date: October 2003
Study Completion Date: November 2003
Primary Completion Date: November 2003 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Citalopram
Citalopram Hydrobromide Tablets 40 mg of Dr.Reddy's
Drug: Citalopram Hydrobromide
Citalopram Hydrobromide Tablets 40 mg of Dr.Reddy's Laboratories Limited
Other Name: Celexa Tablets 40 mg
Active Comparator: Celexa
Celexa 40 mg Tablets of Forest Labs
Drug: Citalopram Hydrobromide
Citalopram Hydrobromide Tablets 40 mg of Dr.Reddy's Laboratories Limited
Other Name: Celexa Tablets 40 mg

Detailed Description:

randomized, 2-way crossover; bioequivalence study of citalopram hydrobromide 40 mg tablets and celexa 40 mg tablets administered as

1 x 40 mg tablet in healthy subjects under fed conditions.

  Eligibility

Ages Eligible for Study:   18 Years to 45 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

Subjects enrolled in this study will be members of the community at large. The recruitment advertisements may use various media types (e.g. radio, newspaper, Anapharm Inc.Web site, Anaphann Inc. volunteers' data base). Subjects must meet all of the following criteria in order to be included in the study:

  • Non-child-bearing potential female or simale, smokers and/or non-smoker, 18 years of age and older.
  • Subjects capable of consent
  • Non-child-bearing potential female subject:
  • Post-menopausal state: absence of menses for 12 months prior to drug administration or hysterectomy with bilateral oophorectomy at least 6 months prior to drug administration.
  • Surgically sterile: hysterectomy, bilateral oophorectomy, or tubal ligation at least 6 months prior to drug administration.

Exclusion Criteria:

  • Subjects to whom any of the following applies will be excluded from the study:

    • Clinically significant illnesses within 4 weeks prior to the administration of the study medication.
    • Clinically significant surgery within 4 weeks prior to the administration of the study medication.
    • Any clinically significant abnormality found during medical screening.
    • Any reason which, in the opinion of the Medical Sub-Investigator, would prevent the subject from participating in the study.
    • Abnormal laboratory tests judged clinically significant.
    • Positive urine drug screen at screening.
    • Positive testing for hepatitis B, hepatitis C, or Human Immunodeficiency Virus HIV) at screening.
    • ECG abnormalities (clinically significant) or vital sign abnormalities (systolic blood pressure lower than 90 or over 140 mmHg, diastolic blood pressure lower than 50 or over 90 mmHg, or heart rate less than 50 or over 100 bpm)at screening.
    • Subjects with Body Mass Index (BMI) 2:30.0.
    • History of significant alcohol abuse within six months prior to the screening visit or any indication of the regular use of more than fourteen units of alcohol per week (1 Unit = 150 mL of wine, 360 mL of beer, or 45 mL of 40% alcohol).
    • History of drug abuse or use of illegal drugs: use of soft drugs (such as marijuana) within 3 months prior to the screening visit or hard drugs (such as cocaine, phencyclidine [PCP]and crack) within 1 year prior to the screening visit.
    • History of allergic reactions to citalopram hydrobromide or other related drugs.
    • History of allergic reactions to heparin.
    • Use of any drugs known to induce or inhibit hepatic drug metabolism (examples of inducers: barbiturates, carbamazepine, phenytoin, glucocorticoids, rifampin/rifabutin; examples of inhibitors: antidepressants, cimetidine, diltiazem, erythromycin, ketoconazole, Mono Amine Oxidase (MAO) inhibitors, neuroleptics, verapamil, quinidine) within 30 days prior to administration of the study medication.
    • Use of an investigational drug or participation in an investigational study within 30 days prior to administration of the study medication.
    • Clinically significant history or presence of any clinically significant gastrointestinal pathology (e.g. chronic diarrhea, inflammatory bowel diseases). Unresolved gastrointestinal symptoms (e.g. diarrhea, vomiting), liver or kidney disease, or other conditions known to interfere with the absorption, distribution, metabolism, or excretion of the drug.
    • Any clinically significant history or presence of clinically significant neurological,endocrinal, cardiovascular, pulmonary, hematologic, immunologic psychiatric or metabolic disease.
    • Use of prescription medication (including hormone therapy) within 14 days prior to administration of study medication or over-the-counter products (including natural food supplements, vitamins, garlic as a supplement) within 7 days prior to administration of study medication, except for topical products without systemic absorption.
    • Smoking more than 25 cigarettes per day.
    • Any food allergy, intolerance, restriction or special diet that could, in the opinion of the Medical Sub-Investigator, contraindicate the subject's participation in this study.
    • A depot injection or an implant of any drug within 3 months prior to administration of study medication.
    • Donation of plasma (500 mL) within 7 days prior to drug administration. Donation or loss of whole blood prior to administration of the study medication as follows:
    • less than 300 mL of whole blood within 30 days,
    • 300 mL to 500 mL of whole blood within 45 days or
    • more than 500 mL of whole blood within 56 days prior to drug administration.
    • Consumption of food or beverages containing grapefruit (e.g. fresh, canned or frozen)within 7 days prior to administration of the study medication.
    • History of seizure disorder or bipolar affective disorder.
    • Active psychiatric diagnosis.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01149980

Locations
Canada
Anapharm
Quebec, Canada
Sponsors and Collaborators
Dr. Reddy's Laboratories Limited
Investigators
Principal Investigator: Benoit Girard, M.D Anapharm. Clinical Laboratory
  More Information

No publications provided

Responsible Party: Dr.Ramakrishna Banagaru, Dr. Reddy's Laboratories Limited
ClinicalTrials.gov Identifier: NCT01149980     History of Changes
Other Study ID Numbers: 30285
Study First Received: June 21, 2010
Last Updated: June 23, 2010
Health Authority: United States: Food and Drug Administration

Keywords provided by Dr. Reddy's Laboratories Limited:
Bioequivalence
Crossover
Citalopram

Additional relevant MeSH terms:
Citalopram
Dexetimide
Antidepressive Agents, Second-Generation
Antidepressive Agents
Psychotropic Drugs
Central Nervous System Agents
Therapeutic Uses
Pharmacologic Actions
Serotonin Uptake Inhibitors
Neurotransmitter Uptake Inhibitors
Neurotransmitter Agents
Molecular Mechanisms of Pharmacological Action
Serotonin Agents
Physiological Effects of Drugs
Antiparkinson Agents
Anti-Dyskinesia Agents
Parasympatholytics
Autonomic Agents
Peripheral Nervous System Agents
Muscarinic Antagonists
Cholinergic Antagonists
Cholinergic Agents

ClinicalTrials.gov processed this record on April 16, 2014