Bioequivalence Study of Zolpidem Tartrate Tablets and Ambien® Under Fasting Conditions

Phase 1

Completed

• Conditions: Healthy
• Interventions: Drug: Zolpidem Tartrate 10 mg tablet; Drug: Zolpidem Tartrate 10 mg tablet (Ambien®)

• Registration Number: NCT00684814
• Lead Sponsor: Mutual Pharmaceutical Company, Inc.

Brief Summary

The purpose of this study is to compare the bioequivalence of a test formulation of zolpidem tartrate tablets to an equivalent oral dose of the commercially available reference drug product Ambien® (zolpidem tartrate tablets) in adult subjects under fasted conditions.

Detailed Description

The purpose of this study is to compare the bioequivalence of a test formulation of zolpidem tartrate tablets to an equivalent oral dose of the commercially available reference drug product Ambien® (zolpidem tartrate tablets) in adult subjects under fasted conditions.

Thirty-eight healthy, non-smoking, non-obese male and female volunteers at least 18 years of age will be randomly assigned in a crossover fashion to receive each of two zolpidem tartrate dosing regimens in sequence with a 7 day washout period between dosing periods. On the morning of Day 1, after an overnight fast of at least 10 hours, subjects will receive either a single oral dose of the test formulation, zolpidem tartrate (1 x 10 mg tablet) or a single oral dose of the reference formulation, Ambien® (1 x 10 mg tablet). After a 7 day washout period, on the morning of Day 8 after an overnight fast, subjects will receive the alternate regimen. Blood samples will be drawn from all participants before dosing and for 12 hours post dose at times sufficient to adequately define the pharmacokinetics of zolpidem tartrate. A further goal of this study is to evaluate the safety and tolerability of this regimen in healthy volunteers. Subjects will be monitored throughout the confinement portion of the study for adverse reactions to the study drugs and/or procedures. Blood pressure and pulse rate will be obtained prior to dosing and at 0.5, 1, 2, 4 and 12 hours post-dose. All adverse events whether elicited by query, spontaneously reported or observed by clinic staff will be evaluated by the investigator and reported in the subject's case report form.

Study Timeline

• Study Start: 2004-05
• Primary Completion: 2004-05
• Study Completion: 2004-05
• Study First Submitted: 2008-05-24
• Study First Submitted QC: 2008-05-27
• Study First Posted: 2008-05-28
• Results First Submitted: 2009-12-04
• Results First Submitted QC: 2009-12-04
• Results First Posted: 2010-01-08
• Status Verified: 2012-04
• Last Update Submitted: 2012-04-18
• Last Update Posted: 2012-04-20

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 38

Inclusion Criteria

• Sex: Male or Female; similar proportions of each preferred
• Age: At least 18 years
• Weight: must be 15% of ideal weight for height and frame
• Subjects must be in good health and physical condition as determined by medical history
• Subjects must read and sign the Consent Form

Exclusion Criteria

• History of treatment for alcoholism, substance abuse, or drug abuse within past 24 months.
• History of malignancy, stroke, diabetes, cardiac, renal or liver disease, or other serious illness.
• History of GERD, malabsorption syndrome, colon cancer, or chronic colitis, including Crohn's disease.
• History of treatment for asthma within the past five (5) years.
• History of mental depression.
• History of pulmonary disease.
• History of sleep apnea.
• Females who are pregnant or lactating.
• History of hypersensitivity to zolpidem tartrate, or any hypnotic or sedative.
• Treatment with any other investigational drug during the four weeks prior to the initial dosing of the study.
• Donation of blood within four weeks prior to the initial dosing of the study
• Smokers or subjects who use tobacco/nicotine products. Three months abstinence is required.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Arm && Interventions

Group	Intervention	Description
Zolpidem Tartrate 10 mg Tablets	Zolpidem Tartrate 10 mg tablet	A single dose of zolpidem tartrate 10 mg administered after an overnight fast of at least 10 hours.
Zolpidem Tartrate (Ambien®) 10 mg Tablets	Zolpidem Tartrate 10 mg tablet (Ambien®)	A single dose of Ambien® 10 mg administered after an overnight fast of at least 10 hours.

Primary Outcome Measures

Name	Time	Method
Maximum Plasma Concentration (Cmax) for Zolpidem Tartrate	serial pharmacokinetic blood samples drawn prior to dosing (hour 0), and then at 0.25, 0.5, 0.75, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 2.75, 3, 3.25, 3.5, 4, 5, 6, 8, 10, and 12 hours after dose administration	The maximum or peak concentration that zolpidem tartrate reaches in the plasma.
Area Under the Concentration Versus Time Curve From Time 0 to Time t [AUC(0-t)] for Zolpidem Tartrate	serial pharmacokinetic blood samples drawn prior to dosing (hour 0), and then at 0.25, 0.5, 0.75, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 2.75, 3, 3.25, 3.5, 4, 5, 6, 8, 10, and 12 hours after dose administration	The area under the plasma concentration versus time curve, from time 0 to the time of the last measurable zolpidem tartrate concentration (t), as calculated by the linear trapezoidal rule.
Area Under the Concentration Versus Time Curve From Time 0 Extrapolated to Infinity [AUC(0-∞)]for Zolpidem Tartrate	serial pharmacokinetic blood samples drawn prior to dosing (hour 0), then 0.25, 0.5, 0.75, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 2.75, 3, 3.25, 3.5, 4, 5, 6, 8, 10, and 12 hours after dose administration	The area under the zolpidem tartrate plasma concentration versus time curve from time 0 to infinity. AUC(0-∞) was calculated as the sum of AUC(0-t) plus the ratio of the last measurable plasma concentration to the elimination rate constant.