Status:
COMPLETED
Bioequivalence Study of Levomerc 500 mg Tablets
Lead Sponsor:
University of Karachi
Collaborating Sponsors:
Merck Pvt. Ltd, Pakistan
Center for bioequivalence studies and clinical reseach (CBSCR), ICCBS, University of Karachi
Conditions:
Healthy
Pharmacokintetics
Eligibility:
All Genders
18-50 years
Phase:
PHASE1
Brief Summary
An open Label, Randomized, Two Way Cross over, Two Period, Two Treatment, two Sequence Bioequivalence Study of Levomerc tablets (Levofloxacin) 500 mg compared with Tavanic (Levofloxacin) 500 mg Tablet...
Detailed Description
The study will be conducted on 24 healthy subjects. The study will comprise of two Periods, I and II, each consisting of 36 hours, 12 hours before and 24 hour after the drug administration. All 24 sub...
Eligibility Criteria
Inclusion
- All subjects should be healthy and free from any epidemic, contagious or measurable disease (e.g. Malaria, Dengue).
- Age range for inclusion will be 18-50 year.
- BMI for all Subjects will be between 18.5-26.9 kg/ m2.
- Non Smokers, who have not smoked in last 3 months.
- Medical history, physical examination and screening tests must fall in normal range, unless the investigator considers the abnormality to be clinically not significant.
- Clinical laboratory test result should be within a normal range.
- Participants (who can read and understand Urdu) should be able to give informed consent, understand and sign the Informed Consent Form.
- Participants should have adequate organ function (i.e., kidney, liver and heart).
Exclusion
- Age and/or BMI out of acceptable range.
- Any active allergic disease or a history of any significant allergic disease (e.g. Rhinitis, dermatitis, asthma).
- Known hypersensitivity to Investigational drug(s).
- Abnormal results of blood and urine tests conducted at screening unless the investigator considers an abnormality to be clinically irrelevant.
- Presence or history of cardiac (e.g. Myocardial Infarction, arrythmia), renal (e.g. renal insufficiency) , hepatic (e.g. hepatic impairment) , organ insufficiency, bone marrow disease, hematological abnormality (e.g. leukemia, anemia), photosensitivity, neurological disorders (e.g. Alzheimer's disease) or gastrointestinal disease known to interfere with the drug absorption, distribution, metabolism or elimination (e.g. dysphagia).
- History or presence of any musculo skeletal disease (e.g. Tendonitis).
- Subject donated blood (450ml) within 12 weeks minimum preceding the study.
- Alcoholic or with a history of chronic alcohol intake or consumed alcohol or Gutka in last 3 months.
- Ingestion of OTC drug, within 14 days of drug administration (e.g. aspirin, ibuprofen).
- History of intake of any prescribed medicine (e.g. captopril, sumatriptan) during a period of 30 days, prior to drug administration day of study.
- Ingestion of investigational drug within 30 days, prior to investigational drug administration in the study.
- Ingestion of any known hepatic or renal clearance altering agents (e.g. erythromycin, cimetidine, barbiturates, phenothiazines, etc.) for a period of 30 days, prior to study initiation.
- Subjects with an uncontrolled medical condition (i.e., hypertension, cardiac arrhythmias, CHF) that places the patient at risk by participating in the study.
- xiv. Subjects with known HIV, hepatitis B or C infection or autoimmune diseases.
- History of drug exposure which, in the opinion of Investigator, amounts to drug abuse. -
- Participation in other drug studies within three months prior to study initiation.
- Subjects with any physical/mental disability.
- Limited mental capacity to the extent that the subject is unable to provide legal consent and information regarding the side effects or tolerance of the study drug.
- Pregnancy or breast feeding, women of child bearing age who are not using a recognized form of contraception for at least last 30 days or using hormonal contraception, are also excluded.
Key Trial Info
Start Date :
July 11 2012
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 20 2012
Estimated Enrollment :
24 Patients enrolled
Trial Details
Trial ID
NCT05339295
Start Date
July 11 2012
End Date
September 20 2012
Last Update
September 7 2022
Active Locations (1)
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1
Center for Bioequivalence Studies and clinical research (CBSCR), ICCBS
Karachi, Sindh, Pakistan, 75270