Bioequivalence Study of Carvedilol 12.5mg Tablets Under Fed Conditions

NCT00775619 | Completed DMC

• 1 other identifier: 023/CARVE-12.5/03
• Study Type: interventional
• Target: 40
• Locations: 0 countries
• Sites: N/A

Brief Summary

The objective of this study was to compare the single-dose oral bioavailability of Carvedilol 12.5 mg tablets of Ranbaxy Laboratories with Coreg 12.5 mg tablets of Glaxosmithkline in healthy, adult, human subjects under fed conditions.

Conditions

Healthy

Keywords

bioequivalence Carvedilol 12.5 mg tablets fed conditions

Outcome Measures

Primary Outcomes (1)

• Bioequivalence

Study Arms (2)

2

ACTIVE COMPARATOR

Coreg® 12.5 mg tablets

Drug: Carvedilol 12.5 mg tablets

1

EXPERIMENTAL

Carvedilol 12.5 mg tablets

Drug: Carvedilol 12.5 mg tablets

Interventions

Carvedilol 12.5 mg tablets DRUG

bioequivalence Carvedilol 12.5 mg tablets fed conditions

1; 2

Eligibility Criteria

• Age: 18 Years - 45 Years
• Sex: male
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Be in the' age range of 18-45 years.
• Be neither overweight nor underweight for his/her height as per the Life Insurance Corporation of lndia height/weight chart for non-medical cases.
• Have voluntarily given written informed consent to participate in this study.
• Be of normal health as determined by medical history and physical examination of the subjects performed within :1.4 days prior to the commencement of the study.
• If female and:
• Of childbearing potential, is practicing an acceptable method of birth control for the duration of the study as judged by the investigator(s), such as condoms, foams, jellies, diaphragm, intrauterine device (\[UD), or abstinence; or Is postmenopausal for at least 1 year; or
• Is surgically sterile (bilateral tubal ligation, bilateral oophorectomy, or hysterectomy).

You may not qualify if:

• History of allergy to 13-adrenoceptor antagonists especially carvedilol.
• 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 and 2, Hepatitis B and C viruses or syphilis infection.
• Female volunteers demonstrating a positive pregnancy test.
• Female volunteers who are currently breastfeeding.
• Presence of values which are significantly different from normal reference ranges (as defined in Appendix 5) 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 And cannabinoids)
• Presence of values which are significantly different from normal reference ranges (as defined in Appendix 5) 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, glaucoma, bronchial asthma, fainting or syncope.
• History of any psychiatric illness which may impair the ability to provide written informed consent.
• Regular smokers who smoke more than 10 cigarettes daily or have difficulty abstaining from smoking for the duration of each study period.
• History of drug dependence or excessive alcohol intake on Habitual basis of more than 2 units of alcoholic beverages per day (1 Unit equivalent to half pint of beer or ! glass of wine or I measure of spirit) or have difficulty\_ in abstaininq for the duration of each study period.
• Use of any enzyme modifying drugs within 30 days prior to Day 1 of this study.

Sponsors & Collaborators

• Ranbaxy Laboratories Limited: lead

Related Links

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MeSH Terms

Interventions

Carvedilol

Intervention Hierarchy (Ancestors)

Propanolamines; Amino Alcohols; Alcohols; Organic Chemicals; Propanols; Amines; Carbazoles; Indoles; Heterocyclic Compounds, 2-Ring; Heterocyclic Compounds, Fused-Ring; Heterocyclic Compounds; Heterocyclic Compounds, 3-Ring

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: NONE
• Intervention Model: CROSSOVER
• Sponsor Type: INDUSTRY

Study Record Dates

• First Submitted: October 16, 2008
• First Posted: October 20, 2008
• Study Start: September 1, 2003
• Primary Completion: September 1, 2003
• Study Completion: December 1, 2003
• Last Updated: October 20, 2008

Record last verified: 2008-10