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Clinical Trials/NCT00739648
NCT00739648
Completed
Phase 2

Phase 2, Randomized, Double-Blind, Placebo-Controlled, Study to Evaluate the Safety, Tolerability and Efficacy of MP-376 Inhalation Solution Administered for 5 Days Every 28 Days to Prevent Acute Exacerbations in High Risk COPD Patients

Amgen0 sites322 target enrollmentOctober 2008

Overview

Phase
Phase 2
Intervention
Placebo
Conditions
Chronic Obstructive Pulmonary Disease
Sponsor
Amgen
Enrollment
322
Primary Endpoint
Exacerbation Rate
Status
Completed
Last Updated
last year

Overview

Brief Summary

Patients with Chronic Obstructive Pulmonary Disease (COPD) suffer from frequent and recurrent acute exacerbations (AECB) which are associated with enormous healthcare expenditures and significant morbidity, specifically an increased risk of death, a decline in pulmonary function and a significant change in quality of life. Bacteria appear to have an important role in acute exacerbations in chronic bronchitis and COPD. Studies of acute exacerbations in COPD have shown a reduction in bacterial load with prolonged exacerbation-free interval. In addition, recent studies indicate that acquisition of a new strain of H. influenzae, M. catarrhalis, S. pneumoniae or P. aeruginosa are responsible for many of these exacerbations. Chronic inflammation and bacterial infection predispose many patients to frequent and recurrent acute exacerbations.

Mpex believes that intermittent administration of inhaled MP-376 in high risk patients will decrease the incidence of acute exacerbations by both by lowering the organism burden, and resultant inflammation, as well as pre-emptive eradication of any newly acquired bacterial strains.

Detailed Description

This study will be a Phase 2, multi-center, randomized, double-blind, placebo-controlled study to evaluate the safety, tolerability, and efficacy of MP-376 inhalation solution given daily for 5 days in a 28 day treatment cycle to COPD patients. Study with completed results acquired from Horizon in 2024.

Registry
clinicaltrials.gov
Start Date
October 2008
End Date
April 2010
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Amgen
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Arms & Interventions

Placebo

Placebo inhaled twice daily via the PARI eFlow nebulizer for 5 consecutive days within a 28-day treatment cycle for up to 12 cycles

Intervention: Placebo

MP-376 240 mg Twice Daily (BID)

MP-376 240 mg BID inhaled via the PARI eFlow nebulizer for 5 consecutive days within a 28-day treatment cycle for up to 12 cycles

Intervention: MP-376

Outcomes

Primary Outcomes

Exacerbation Rate

Time Frame: From randomization to the patients final study visit (up to 12 months)

The number of acute exacerbations per patient-year of study participation, where an acute exacerbation was defined as a deterioration in respiratory symptoms that required treatment with antibiotics, corticosteroids, hospitalization or a combination of those treatments.

Secondary Outcomes

  • Duration of Acute Exacerbation(from randomization to the patient's final study visit (up to 12 months))
  • Percent Change in Forced Expiratory Volume in 1 Second (FEV1)(from baseline to the conclusion of the fourth 28-day treatment cycle (4 months))
  • Percent Change in Forced Vital Capacity (FVC)(from baseline to the conclusion of the fourth 28-day treatment cycle (4 months))

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