Efficacy and Safety of Subcutaneous Secukinumab in Adults With Moderate to Severe Scalp Psoriasis



Status:Completed
Conditions:Psoriasis
Therapuetic Areas:Dermatology / Plastic Surgery
Healthy:No
Age Range:18 - Any
Updated:12/15/2017
Start Date:September 2014
End Date:December 2015

Use our guide to learn which trials are right for you!

A Randomized, Double-blind, Placebo-controlled, Parallel-group, Multicenter Study to Demonstrate the Efficacy of Subcutaneous Secukinumab [300 mg] as Assessed by the Psoriasis Scalp Severity Index (PSSI) at 12 Weeks of Treatment, Compared to Placebo, and to Assess Safety and Tolerability up to 24 Weeks in Adult Subjects With Moderate to Severe Scalp Psoriasis

This study will assess the efficacy and safety of secukinumab compared to placebo in adult
patients who have moderate to severe scalp psoriasis that is poorly controlled by current
psoriasis treatments.


Inclusion Criteria:

- Chronic scalp psoriasis for at least the previous six months

- Moderate to severe scalp psoriasis as defined by a PSSI score of ≥12 and 30% or higher
of scalp surface area affected

- Must be candidates for systemic therapy, which means having scalp psoriasis
inadequately controlled by topical treatments (corticosteroids), and/or phototherapy,
and/or previous systemic therapy.

Exclusion Criteria:

- Forms of psoriasis other than chronic plaque

- Drug-induced psoriasis (e.g., new onset or current exacerbation from β-blockers,
calcium channel inhibitors)

- Ongoing use of prohibited treatments (e.g., topical or systemic corticosteroids, UV
therapy)

- Prior exposure to secukinumab (AIN457) or any other biologic drug directly targeting
IL17A or IL-17RA receptors

- Use of other investigational drugs within 30 days prior to study entry, or within a
period of 5 half-lives of the investigational treatment, whichever is longer

- Active, ongoing inflammatory diseases other than psoriasis that might confound the
evaluation of the benefit of secukinumab

- Active system infections (with the exception of the common cold) during the two weeks
prior to starting study treatment

- Other protocol-defined inclusion/exclusion criteria may apply
We found this trial at
16
sites
Arlington, Texas 76012
?
mi
from
Arlington, TX
Click here to add this to my saved trials
Andover, Massachusetts 01810
?
mi
from
Andover, MA
Click here to add this to my saved trials
Aurora, Colorado 80010
?
mi
from
Aurora, CO
Click here to add this to my saved trials
Boston, Massachusetts 02118
?
mi
from
Boston, MA
Click here to add this to my saved trials
East Windsor, New Jersey 08520
?
mi
from
East Windsor, NJ
Click here to add this to my saved trials
Gahanna, Ohio 43230
?
mi
from
Gahanna, OH
Click here to add this to my saved trials
Hershey, Pennsylvania 17033
?
mi
from
Hershey, PA
Click here to add this to my saved trials
230 Park Avenue, 21st Floor
New York, New York 10169
1-888-669-6682)
Novartis Novartis, which was created in 1996 by the merger of the Swiss companies Ciba-Geigy...
?
mi
from
New York, NY
Click here to add this to my saved trials
230 Park Avenue, 21st Floor
New York, New York 10169
1-888-669-6682)
Novartis Novartis, which was created in 1996 by the merger of the Swiss companies Ciba-Geigy...
?
mi
from
New York, NY
Click here to add this to my saved trials
Rockville, Maryland 20852
?
mi
from
Rockville, MD
Click here to add this to my saved trials
Sacramento, California 95825
?
mi
from
Sacramento, CA
Click here to add this to my saved trials
Salt Lake City, Utah 84103
?
mi
from
Salt Lake City, UT
Click here to add this to my saved trials
Troy, Michigan 48098
?
mi
from
Troy, MI
Click here to add this to my saved trials
Trumbull, Connecticut 06611
?
mi
from
Trumbull, CT
Click here to add this to my saved trials
West Jordan, Utah 84088
?
mi
from
West Jordan, UT
Click here to add this to my saved trials
Winston-Salem, North Carolina 27157
?
mi
from
Winston-Salem, NC
Click here to add this to my saved trials