Status:
COMPLETED
Benazepril HCl 40 mg Tablets, Fasting
Lead Sponsor:
Teva Pharmaceuticals USA
Conditions:
Healthy
Eligibility:
All Genders
18+ years
Phase:
PHASE1
Brief Summary
The objective of this randomized, single-dose, two-way crossover evaluation is to compare the oral bioavailability of a test benazepril HCl formulation (TEVA Pharmaceutical Industries Ltd.) to an equi...
Detailed Description
Criteria for Evaluation: FDA Bioequivalence Criteria Statistical Methods: FDA bioequivalence statistical methods
Eligibility Criteria
Inclusion
- Sex: Male and Female; similar proportions of each preferred.
- Age: At least 18 years.
- Subjects must have a minimum weight of at least 110 pounds.
- Qualifying subjects must be in good health and physical condition as determined by medical history, complete physical examination, and laboratory tests, all obtained within four (4) weeks prior to study start. The subject may not have a history of significant past illness expected to affect the investigation. The normal status of subjects will be confirmed by the following procedures:
- Laboratory Tests: Hemoglobin, hematocrit, RBC, WBC, differential count, serum electrolytes (Na, K, Cl), fasting blood glucose, BUN, bilirubin, creatinine, AST, ALT, LDH, alkaline phosphatase, and urinalysis. HIV, Hepatitis B, Hepatitis C, and drugs of abuse testing will be done for screening purposes only. Laboratory values which are greater than ± 20% of the normal range will not qualify unless specifically accepted (with comment) by the Principal Investigator. Results of HIC, Hepatitis B, Hepatitis C, and drugs of abuse must be negative or non-reactive for the subject to qualify for the study. Additional drugs of abuse testing will be done at check-in for each period. Tests are to be negative as a requirement for dosing. Female subjects will have a urine pregnancy test done at screening and prior to each study period at check-in.
- Electrocardiogram: A 12-lead electrocardiogram will be obtained for all subjects. The original tracings, plus interpretation, will be included in the case report form packet.
- Subjects must read and sign the Consent Form.
Exclusion
- Subjects no complying with the above inclusion criteria must be excluded from the study.
- In addition one of the conditions listed below will exclude a subject from the study:
- History of treatment for alcoholism, drug abuse, or substance abuse within the past 24 months.
- History of malignancy, stroke, diabetes, cardiac, renal or liver disease, or other serious illness.
- History of treatment for asthma within the past five (5) years.
- History of treatment for any gastrointestinal disorder within the past five (5) years.
- History of neutropenia.
- History of hyperkalemia.
- History of angioedema.
- History of impaired renal function.
- History of persistent nonproductive cough.
- Females who are pregnant or lactating.
- History of hypersensitivity to benazepril HCl, or any angiotensin-converting enzyme (ACE) inhibitor.
- Conditions upon screening which might contraindicate or require that caution be used in the administration of benazepril HCl, including:
- Sitting systolic blood pressure below 90 mmHg, or diastolic pressure below 50 mmHg.
- Heart rate less than 50 beats per minute after a 5-minute rest in a seated position.
- Inability to read and/or sign the consent form.
- Treatment with any other investigational drug during the four (4) weeks prior to enrollment into the study.
- Subjects who have donated blood within four (4) weeks prior to entry into the study.
Key Trial Info
Start Date :
February 1 2001
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 1 2001
Estimated Enrollment :
40 Patients enrolled
Trial Details
Trial ID
NCT00836576
Start Date
February 1 2001
End Date
March 1 2001
Last Update
August 19 2024
Active Locations (1)
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1
Gateway Medical Research, Inc.
Saint Charles, Missouri, United States, 63301