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Clinical Trials/NCT00752414
NCT00752414
Completed
Phase 1

Phase 1b, Randomized, Single-Blind, Placebo-Controlled, Study to Evaluate the Safety, Tolerability and Pharmacokinetics of MP-376 Inhalation Solution Administered for 5 Days to Chronic Bronchitis Patients

Amgen0 sites21 target enrollmentJuly 2008

Overview

Phase
Phase 1
Intervention
MP-376 (Levofloxacin solution for Inhalation)
Conditions
Chronic Obstructive Pulmonary Disease
Sponsor
Amgen
Enrollment
21
Primary Endpoint
Evaluate the safety, tolerability and PK of two dosage regimens of MP-376
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, (the sponsor on record at time of the study's initial registration) 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 1b, multi-center, randomized, single-blind, placebo-controlled study to evaluate the safety, tolerability, and pharmacokinetics of MP-376 solution for inhalation given for 5 days to COPD patients. Study acquired from Horizon in 2024.

Registry
clinicaltrials.gov
Start Date
July 2008
End Date
October 2008
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

1

MP-376 Inhalation Solution

Intervention: MP-376 (Levofloxacin solution for Inhalation)

2

Placebo

Intervention: Placebo

Outcomes

Primary Outcomes

Evaluate the safety, tolerability and PK of two dosage regimens of MP-376

Time Frame: 2 weeks

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