Clinical Trials Directory

Trials / Completed

CompletedNCT02359292

Clinical Pharmacology Study to Evaluate the Total Systemic Exposure and Lung Bioavailability of CHF 5993 pMDI Combination in Healthy Volunteers

Cross-over Clinical Pharmacology Study, to Evaluate the Total Systemic Exposure and Lung Bioavailability of CHF 5993 pMDI Combination Across Two Different Dose Strengths, Administered With and Without Activated Charcoal, in Healthy Volunteers

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
50 (actual)
Sponsor
Chiesi Farmaceutici S.p.A. · Industry
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

The study is performed to evaluate the total systemic exposure and lung bioavailability of CHF 5993 pMDI combination, in healthy volunteers subjects.

Conditions

Interventions

TypeNameDescription
DRUGCHF 5993 HS 200/6/25 pMDI
DRUGCHF 5993 MS 100/6/25 pMDI
DRUGCHF 5993 HS 200/6/25 pMDI + Charcoal Block
DRUGCHF 5993 MS 100/6/25 pMDI + Charcoal Block
DRUGPlacebo pMDI

Timeline

Start date
2015-02-01
Primary completion
2015-04-01
Completion
2015-07-01
First posted
2015-02-10
Last updated
2021-07-02

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT02359292. Inclusion in this directory is not an endorsement.