L-CsA for Prevention of Bronchiolitis Obliterans Syndrome Following LT
Research type
Research Study
Full title
A phase II, multicentre, randomised, double-blind, placebo controlled, parallel group, dose-finding clinical trial to investigate the efficacy and safety of 10 and 20 mg/day aerosolised liposomal ciclosporin A (L-CsA) versus aerosolised placebo in the prevention of bronchiolitis obliterans syndrome (BOS) in lung transplant (LT) patients
IRAS ID
15267
Sponsor organisation
PARI Pharma GmbH
Eudract number
2008-003800-73
ISRCTN Number
66069132
Clinicaltrials.gov Identifier
N/A
Research summary
N/A
REC name
East of England - Cambridge East Research Ethics Committee
REC reference
09/H0304/47
Date of REC Opinion
27 Aug 2009
REC opinion
Further Information Favourable Opinion