Study of Safety, Tolerability, and Efficacy of Secukinumab in Subjects With Moderate to Severe Palmoplantar Psoriasis

PHASE3CompletedINTERVENTIONAL
Enrollment

205

Participants

Timeline

Start Date

June 19, 2013

Primary Completion Date

November 2, 2016

Study Completion Date

November 2, 2016

Conditions
Moderate to Severe Palmoplantar Psoriasis
Interventions
BIOLOGICAL

secukinumab 150 mg

Study treatment were provided in pre-filled syringes of secukinumab 150 mg in 1 mL. Each dosing consiseds of one secukinumab 150 mg s.c. injection plus one placebo secukinumab s.c. injection and took place once weekly during five weeks (at Baseline, Weeks 1, 2, 3 and 4), then once every four weeks starting at Week 8 until Week 128 inclusive. In order to maintain the blinding, patients also received two placebo injections at Weeks 17, 18 and 19. Patients self-administered study treatment under the supervision of site personnel when injections occur during study visits, or at home otherwise.

BIOLOGICAL

secukinumab 300 mg

Study treatment were provided in pre-filled syringes of secukinumab 150 mg in 1 mL. Each dosing consisted of two secukinumab 150 mg s.c. injections and took ke place once weekly during five weeks (at Baseline, Weeks 1, 2, 3 and 4), then once every four weeks starting at Week 8 until Week 128 inclusive. In order to maintain the blinding, patients also receives two placebo injections at Weeks 17, 18 and 19. Patients self-administered study treatment under the supervision of site personnel when injections occur during study visits, or at home otherwise.

BIOLOGICAL

Placebo

Placebo were provided in 1 mL pre-filled syringes. Each dosing consisted of two s.c. injections and took place once weekly during five weeks (at Baseline, Weeks 1, 2, 3 and 4), then at Week 8 and at Week 12. At Week 16, ppIGA responders continued on placebo with dosing at Weeks 16, 17, 18, 19 and 20, then once every four weeks from Week 24 until Week 76 inclusive. At Week 80, ppIGA responders ended their participation in the study while ppIGA non-responders were re-randomized, to receive 150 mg or 300 mg secukinumab once every four weeks starting at Week 80 until Week 128 inclusive. Patients self-administered study treatment under the supervision of site personnel when injections occur during study visits, or at home otherwise.

Trial Locations (54)

1134

Novartis Investigative Site, Budapest

1200

Novartis Investigative Site, Brussels

2010

Novartis Investigative Site, Sydney

3002

Novartis Investigative Site, East Melbourne

3053

Novartis Investigative Site, Carlton

3529

Novartis Investigative Site, Miskolc

4000

Novartis Investigative Site, Liège

4032

Novartis Investigative Site, Debrecen

4068

Novartis Investigative Site, Stavanger

4102

Novartis Investigative Site, Woolloongabba

4818

Novartis Investigative Site, Breda

27262

Novartis Investigative Site, High Point

27310

Novartis Investigative Site, Gaziantep

33100

Novartis Investigative Site, Tampere

34093

Novartis Investigative Site, Fatih / Istanbul

34098

Novartis Investigative Site, Istanbul

35010

Novartis Investigative Site, Las Palmas de Gran Canaria

35205

Novartis Investigative Site, Birmingham

40291

Novartis Investigative Site, Louisville

46256

Novartis Investigative Site, Indianapolis

49100

Novartis Investigative Site, Petah Tikva

64239

Novartis Investigative Site, Tel Aviv

85032

Novartis Investigative Site, Phoenix

107076

Novartis Investigative Site, Moscow

119071

Novartis Investigative Site, Moscow

194044

Novartis Investigative Site, Saint Petersburg

420012

Novartis Investigative Site, Kazan'

1834111

Novartis Investigative Site, Afula

6209804

Novartis Investigative Site, Tel Aviv

02111

Novartis Investigative Site, Boston

07044

Novartis Investigative Site, Verona

37072-2301

Novartis Investigative Site, Goodlettsville

T2S 3B3

Novartis Investigative Site, Calgary

L4M 6L2

Novartis Investigative Site, Barrie

N6A 3H7

Novartis Investigative Site, London

N2J 1C4

Novartis Investigative Site, Waterloo

H3Z 2S6

Novartis Investigative Site, Montreal

00250 HUS

Novartis Investigative Site, Helsinki

H-6725

Novartis Investigative Site, Szeged

1105 AZ

Novartis Investigative Site, Amsterdam

3015 CE

Novartis Investigative Site, Rotterdam

3000-075

Novartis Investigative Site, Coimbra

1649-035

Novartis Investigative Site, Lisbon

1998 - 018

Novartis Investigative Site, Lisbon

4099-001

Novartis Investigative Site, Porto

4200 319

Novartis Investigative Site, Porto

040 15

Novartis Investigative Site, Kosice-Saca

04011

Novartis Investigative Site, Košice

089 01

Novartis Investigative Site, Svidník

08916

Novartis Investigative Site, Badalona

08041

Novartis Investigative Site, Barcelona

06500

Novartis Investigative Site, Ankara

E11 1NR

Novartis Investigative Site, London

DY1 2HQ

Novartis Investigative Site, Dudley

Sponsors
All Listed Sponsors
lead

Novartis Pharmaceuticals

INDUSTRY