Overview

Efficacy and Safety of Caspofungin for Invasive Pulmonary Aspergillosis Underlying Chronic Obstructive Pulmonary Disease

Status:
Unknown status
Trial end date:
2014-11-01
Target enrollment:
0
Participant gender:
All
Summary
The investigators propose to study the efficacy and safety of three-week antifungal therapy with caspofungin in hospitalized patients with proven or probable IPA underlying chronic obstructive pulmonary disease.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
The First Affiliated Hospital of Guangzhou Medical University
Collaborator:
Merck Sharp & Dohme Corp.
Treatments:
Caspofungin
Echinocandins
Criteria
Inclusion Criteria:

- Proven invasive pulmonary aspergillosis

- Probable invasive pulmonary aspergillosis

- Hospitalized in respiratory wards

- Not having received an empirical antifungal therapy for 72h before inclusion

Exclusion Criteria:

- A history of allergy to echinocandins

- Severe renal failure, severe hepatic insufficiency

- Inadequately treated bacterial infection

- Documented HIV infection

- Status of pregnancy or lactation