Efficacy of secukinumab compared to ustekinumab in mod/seve psoriasis.
Research type
Research Study
Full title
A 52-week, multicenter, randomized, double-blind study of subcutaneous secukinumab to demonstrate efficacy as assessed by Psoriasis Area and Severity Index at 16 weeks of treatment compared to ustekinumab and to assess long-term safety, tolerability and efficacy in subjects with moderate to severe plaque psoriasis
IRAS ID
141917
Contact name
Benjamin Walker
Contact email
Sponsor organisation
Novartis Pharma Services AG
Eudract number
2013-003434-32
ISRCTN Number
n/a
Clinicaltrials.gov Identifier
n/a
REC name
East Midlands - Nottingham 2 Research Ethics Committee
REC reference
14/EM/0032
Date of REC Opinion
27 Feb 2014
REC opinion
Further Information Favourable Opinion