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
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.
Investigators
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