ADASUVE 2-dose Thorough QT/QTc Study

• Status: Completed
• Trial end date: 2013-07-01
• Target enrollment: 0
• Participant gender: All

Summary

Assess the potential effects on the QT interval of 2 consecutive doses of ADASUVE administered 2 hours apart, in relation to placebo and an active control in healthy volunteers.

• Phase: Phase 4
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: Alexza Pharmaceuticals, Inc.
• Treatments: Fluoroquinolones; Loxapine; Moxifloxacin; Norgestimate, ethinyl estradiol drug combination

Criteria

Inclusion Criteria:

• Male and female subjects between the ages of 18 to 65 years, inclusive.

• Body mass index (BMI) ≥18 and ≤32.

• Subjects who are willing and able to comply with the study schedule and requirements, and stay at the CRU for a 4-day period and 2 consecutive 3-day periods.

• Subjects who speak, read, and understand English and/or Dutch and are willing and able to provide written informed consent on an IEC approved form prior to the initiation of any study procedures.

• Subjects who are in good general health prior to study participation

• Female or male participants who agree to use a medically acceptable and effective birth control method

Exclusion Criteria:

• Subjects who regularly consume large amounts of xanthine-containing substances (≥ 5 cups of coffee/day).

• Subjects who have taken prescription or nonprescription medication within 5 days of Visit 2.

• Subjects who have had an acute illness within the last 5 days of Visit 2.

• Subjects who have smoked tobacco within the last 30 days or who have a positive cotinine test.

• Subjects who have a history of HIV, anti-HCV or HbsAg positivity.

• Subjects who have a history within the past 2 years of drug or alcohol dependence or abuse as defined by DSM-IV.

• Subjects who test positive for alcohol or have a positive urine drug screen.

• Subjects who have a history of allergy or intolerance to loxapine or amoxapine or history of bronchospasm following inhaled loxapine treatment.

• Subjects who have an ECG abnormality.

• Subjects who have hypotension, or hypertension.

• Subjects who have a history of unstable angina, syncope, coronary artery disease, myocardial infarction, congestive heart failure, transient ischemic attack, history of convulsions or other neurological disorder.

• Subjects who have a current history of asthma, chronic obstructive lung disease, or any other lung disease associated with bronchospasm.

• Subjects who use medications to treat airways disease, such as asthma or COPD.

• Subjects who have any acute respiratory signs/symptoms (e.g., wheezing).

• Female subjects who have a positive pregnancy test at screening or at admission to any of the treatment visits, or are breastfeeding.

• Subjects who have received an investigational drug within 60 days prior to the Screening Visit.