drugset / Trial / NCT01746095
Efficacy and Safety Study of AeroVanc for the Treatment of Persistent MRSA Lung Infection in Cystic Fibrosis Patients
Phase 2
Completed
87 enrolled
Savara Inc.
Cystic Fibrosis Foundation · collabSynteract, Inc. · collab
RandomizedParallel-groupQuadruple-blindTreatment
Summary
The purpose of this study is to determine whether AeroVanc treatment is safe and effective in reducing the number of MRSA colony forming units in the lungs of cystic fibrosis patients.
Timeline
- Start
- 2013-03
- Primary completion
- 2014-11
- Completion
- 2014-11
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Vancomycin | Other / unclassified | 16 mg | Inhaled |
| Subject | Vancomycin | Other / unclassified | 32 mg | Inhaled |
| Subject | Vancomycin | Other / unclassified | 64 mg | Inhaled |