Study to Evaluate the Safety and Efficacy of Inhaled PT005 in Patients With Chronic Obstructive Pulmonary Disease (COPD)

• Status: Completed
• Trial end date: 2009-05-01
• Target enrollment: 0
• Participant gender: All

Summary

The purpose of this study is to evaluate the safety and efficacy of inhaled PT005 compared to placebo and Formoterol Fumarate (Foradil Aerolizer) in patients with moderate to severe chronic obstructive pulmonary disease (COPD).

• Phase: Phase 1/Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Pearl Therapeutics, Inc.
• Treatments: Formoterol Fumarate

Criteria

Inclusion Criteria:

• Signed written informed consent

• 40 - 80 years of age

• Fluency in written and spoken English

• Females of non-child bearing potential or females of child bearing potential with negative pregnancy test; and acceptable contraceptive methods

• Current/former smokers with at least a 10 pack-year history of cigarette smoking

• A measured post-salbutamol FEV1/FVC ratio of < or = 0.70

• A measured post-salbutamol FEV1 > or = 40 and < or = 80% of predicted normal values

• Demonstrated reversibility to a short acting beta agonist by either >12% and >150 ml improvement in baseline FEV1, 30 minutes following administration of 4 puffs of salbutamol MDI or an absolute improvement of >200 ml in baseline FEV1, 30 minutes following administration of 4 puffs of salbutamol MDI.

• Competent at using the inhalation device

Exclusion Criteria:

• Women who are pregnant or lactating

• Primary diagnosis of asthma

• Alpha-1 antitrypsin deficiency as the cause of COPD

• Active pulmonary diseases

• Prior lung volume reduction surgery

• Abnormal chest X-ray (or CT scan) not due to the presence of COPD

• Hospitalized due to poorly controlled COPD within 24 weeks of Screening

• Poorly controlled COPD in prior 6-weeks, defined as the occurrence of acute worsening of COPD requiring corticosteroids or antibiotics or acute worsening of COPD requiring treatment prescribed by a physician

• Clinically significant medical conditions

• Lower respiratory tract infection requiring antibiotics in past 6 weeks

• Clinically significant abnormal ECG

• Clinically significant uncontrolled hypertension

• Positive Hepatitis B surface antigen or Hepatitis C antibody

• Cancer that has not been in complete remission for at least 5 years

• History of hypersensitivity to any beta2-agonists or any study drug component

• History of severe milk protein allergy

• Known or suspected history of alcohol or drug abuse

• Medically unable to withhold short acting bronchodilators for 8-hours

• Use of the medications below in specified time interval prior to Screening: 12-weeks:

depot corticosteroids, intra-articular corticosteroids; 4 weeks: ICS >1000 μg/day of fluticasone propionate or equivalent, non-potassium sparing diuretics, P-glycoprotein inhibitors, CYP3A4 inhibitors; 1 week: tiotropium; 48 hours: oral beta agonists, long acting beta agonists, theophylline, zariflukast, montelukast, zileuton; 8 hours: ipratropium or ipratropium/salbutamol combination product, inhaled short acting beta agonists, xanthine containing foods

• Use of the following medications is prohibited: tricyclic antidepressants, monoamine oxidase (MAO) inhibitors, beta-adrenergic antagonists, anticonvulsants (barbiturates,hydantoins, and carbamazepine and phenothiazines

• Receiving long-term-oxygen or nocturnal oxygen therapy for >12 hours a day

• Diagnosis of sleep apnea that is uncontrolled

• Participation in acute phase of pulmonary rehabilitation in prior 4 weeks or will enter acute phase of pulmonary rehabilitation program during study

• Unable to comply with study procedures

• Affiliated with Investigator site

• Questionable validity of consent

• A positive drug of abuse test at Screening lives prior to Screening, whichever is longer