Assessment Of Disease Pathology And Key Therapeutic Targets In Severe Asthma

PHASE1TerminatedINTERVENTIONAL
Enrollment

47

Participants

Timeline

Start Date

August 2, 2005

Primary Completion Date

June 6, 2011

Study Completion Date

June 6, 2011

Conditions
Asthma
Interventions
DRUG

Prednisolone

Subjects will be administered oral prednisolone at a dose of 0.5 mg/kg, up to a maximum of 40 mg per day for 14 days.

PROCEDURE

Bronchoscopy

All subjects will undergo bronchoscopy assessments which will involve insertion of a standard bronchoscope.

Trial Locations (1)

LE3 9QP

GSK Investigational Site, Leicester

Sponsors

Lead Sponsor

All Listed Sponsors
lead

GlaxoSmithKline

INDUSTRY