Chronic Dosing, Cross-Over Study to Assess the Efficacy and Safety of Budesonide (PT008) in Adult Subjects With Mild to Moderate Persistent Asthma
Status: | Active, not recruiting |
---|---|
Conditions: | Asthma |
Therapuetic Areas: | Pulmonary / Respiratory Diseases |
Healthy: | No |
Age Range: | 18 - 65 |
Updated: | 4/21/2016 |
Start Date: | April 2014 |
End Date: | March 2016 |
A Randomized, Double-Blind, Chronic Dosing (4 Weeks), Four-Period, Five-Treatment, Incomplete Block, Cross-Over, Multi-Center Study to Assess the Efficacy and Safety of Four Doses of Budesonide Inhalation Aerosol (BD MDI, PT008) Relative to Placebo MDI in Adult Subjects With Mild to Moderate Persistent Asthma
This is a randomized, double-blind, chronic dosing (4 weeks), four-period, five-treatment,
incomplete block, cross-over, multicenter study to assess the efficacy and safety of four
doses of budesonide inhalation aerosol (BD MDI, PT008) relative to placebo MDI in adult
subjects with mild to moderate persistent asthma.
incomplete block, cross-over, multicenter study to assess the efficacy and safety of four
doses of budesonide inhalation aerosol (BD MDI, PT008) relative to placebo MDI in adult
subjects with mild to moderate persistent asthma.
Inclusion Criteria:
- ≥ 18 - 65 years of age
- Diagnosis of mild to moderate persistent asthma, diagnosed at least 6 months prior to
screening
- Currently receiving treatment with a low to medium dose of an inhaled corticosteroid
(ICS) OR a combination of controller medications for at least 4 weeks preceding
screening
- Pre-albuterol FEV1 of > 60% and < 85% of predicted normal value
- Reversibility: Increase in FEV1 of ≥ 12% and ≥ 200 mL over the pre-albuterol FEV1
within 30 - 60 minutes after the inhalation of 4 puffs of Ventolin hydrofluoroalkane
(HFA)
- Asthma Symptom Criteria: Have required albuterol use on at least two of the last
seven days and have an Asthma Control Questionnaire (ACQ) total score ≥ 1.5 prior to
Randomization
Exclusion Criteria:
- Life-Threatening Asthma: A subject must not have life-threatening asthma defined as a
history of significant asthma episode(s) requiring intubation associated with
hypercapnia, respiratory arrest, hypoxic seizures, or asthma-related syncopal
episode(s) within the 12 months prior to screening
- Worsening of Asthma: A subject must not have experienced a worsening of asthma which
involved an emergency department visit, hospitalization or use of oral/parenteral
corticosteroids within 6 weeks of screening
- Intermittent, Seasonal, or Exercise-Induced Asthma Alone: Subjects with only
intermittent, seasonal or exercise-induced asthma are excluded from participation in
this study
- Concurrent Respiratory Disease
- Pregnant women or nursing mothers
- A current diagnosis of Chronic Obstructive Pulmonary Disease (COPD
- Current smokers or subjects with a > 10 pack year history of cigarettes, cigars, or
pipe smoking
- Respiratory tract infection within 6 weeks prior to Visit 1
- Subjects with documented myocardial infarction within a year from screening visit
- Clinically significant abnormal ECG
- Abnormal liver function tests defined as aspartate aminotransferase (AST), alanine
aminotransferace (ALT), alkaline phosphatase or total bilirubin ≥ 1.5 times upper
limit of normal on repeat testing
- Subjects who have cancer that has not been in complete remission for at least 5 years
- Drug Allergy: Subjects who have a history of hypersensitivity to any component of the
metered-dose inhaler (MDI)
We found this trial at
41
sites
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