A Relative Bioavailability Study of Acetaminophen Extended Release Gel Tabs 650 mg Under Fasting Condition
Information source: Ranbaxy Inc.
ClinicalTrials.gov processed this data on August 23, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Healthy
Intervention: Acetaminophen (Drug)
Phase: N/A
Status: Completed
Sponsored by: Ranbaxy Laboratories Limited
Summary
The study was to compare single-dose oral bioavailability of acetaminophen 650 mg extended
release geltabs (containing acetaminophen 650 mg) of OHM Laboratories Inc. (subsidiary of
Ranbaxy Pharmaceuticals Inc., USA) with Tylenol 8 hour extended release gel tabs (containing
acetaminophen 650 mg) of McNeil Consumer & Speciality Pharmaceuticals, U. S.A in healthy,
adult, male human subjects under fasting condition.
Clinical Details
Official title: An Open Label, Balanced, Randomised, Two-treatment, Two-period, Two-sequence, Single Dose, Crossover Bioavailability Study Comparing Acetaminophen 650 mg Extended Release Gel Tabs (Containing Acetaminophen 650 mg) of OHM Laboratories Inc. (Subsidiary of Ranbaxy) With Tylenol 8 Hour Extended Release Gel Tabs (Containing Acetaminophen 650 mg) of McNeil Consumer & Speciality Pharmaceuticals in Healthy, Adult, Human, Male Subjects Under Fasting Condition
Study design: Allocation: Randomized, Endpoint Classification: Bio-equivalence Study, Intervention Model: Crossover Assignment, Masking: Open Label
Primary outcome: Area under the plasma concentration versus time curve (AUC) and Peak Plasma Concentration (Cmax) of Acetaminophen
Detailed description:
The study was conducted as an open label, balanced, randomised, two-treatment, two-period,
two-sequence, single dose, crossover bioavailability study comparing acetaminophen 650 mg
extended release gel tabs (containing acetaminophen 650 mg) of OHM Laboratories Inc.
(subsidiary of Ranbaxy) with Tylenol 8 hour extended release gel tabs (containing
acetaminophen 650 mg) of McNeil Consumer & Speciality Pharmaceuticals in healthy, adult,
human, male subjects under fasting condition.
The treatments were assigned to the study subjects according to SAS generated randomization
schedule. Each subject received a single oral dose either Test or Reference product in each
period with 240ml of water at ambient temperature after an overnight fast of at least 10
hours under supervision of a trained study personnel.
During the course of the study, safety parameters inclusive of vital signs, clinical
examination, medical history and clinical laboratory safety tests (hematology, biochemical,
serology parameters and urine analysis) at base line were assessed. Laboratory parameters of
hematology and biochemistry were repeated at the end of the study.
Eligibility
Minimum age: 19 Years.
Maximum age: 39 Years.
Gender(s): Male.
Criteria:
Inclusion Criteria:
- Were in the age range of 18-45 years.
- Were neither overweight nor underweight for his height as per the Life Insurance
Corporation of India height/weight chart for non-medical cases.
- Had voluntarily given written informed consent to participate in this study.
- Were of normal health as determined by medical history and physical examination of
the subjects performed within 21 days prior to the commencement of the study.
Exclusion Criteria:
- History of hypersensitivity to Acetaminophen or to any of the components of the
formulation.
- History of skin rashes, thrombocytopenia, urticaria or angioedema
- Any evidence of organ dysfunction or any clinically significant deviation from the
normal, in physical or clinical determinations.
- Presence of disease markers of HIV 1 or 2, Hepatitis B or C viruses or syphilis
infection.
- Presence of values that were significantly different from normal reference ranges
and/or judged clinically significant for haemoglobin, total white blood cells count,
differential WBC count or platelet count.
- Positive for urinary screen testing of drugs of abuse (opiates or cannabinoids)
- Presence of values, which were significantly different from normal reference ranges
and/or judged clinically significant for serum creatinine, blood urea nitrogen, serum
aspartate aminotransferase (AST), serum alanine aminotransferase (ALT), serum
alkaline phosphatase, serum bilirubin, plasma glucose or serum cholesterol.
- Clinically abnormal chemical and microscopic examination of urine defined as presence
of RBC, WBC (> 4/HPF), epithelial cells (> 4/HPF), glucose (positive) or protein
(positive).
- Clinically abnormal ECG or Chest X-ray.
- History of serious gastrointestinal, hepatic, renal, cardiovascular, pulmonary,
neurological or haematological disease, diabetes or glaucoma (rise of pressure inside
the eye leading to blurring or loss of vision)
- History of any psychiatric illness, which might impair the ability to provide written
informed consent.
- Regular smokers who smoked more than 10 cigarettes daily or had difficulty abstaining
from smoking for the duration of each study period.
- History of drug dependence or excessive alcohol intake on a habitual basis of more
than 2 units of alcoholic beverages per day (1 unit equivalent to half pint of beer
or 1 glass of wine or 1 measure of spirit) or had difficulty in abstaining for the
duration of each study period.
- Use of any enzyme modifying drugs within 30 days prior to Day 1 of this study.
- Participation in any clinical trial within 12 weeks preceding Day 1 of this study.
- Subjects who, through completion of this study, would have donated and/or lost more
than 350 mL of blood in the past 3 months.
Locations and Contacts
Clinical Pharmacology Unit, Majeedia Hospital (2nd Floor), New Delhi 110 062, India
Additional Information
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Starting date: May 2006
Last updated: February 8, 2012
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