Psoriasis Clinical Trial

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

Summary

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.

View Eligibility Criteria

Eligibility Criteria

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

Study is for people with:

Psoriasis

Phase:

Phase 3

Estimated Enrollment:

102

Study ID:

NCT02267135

Recruitment Status:

Completed

Sponsor:

Novartis Pharmaceuticals

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There are 17 Locations for this study

See Locations Near You

Novartis Investigative Site
Sacramento California, 95819, United States
Novartis Investigative Site
Aurora Colorado, 80045, United States
Novartis Investigative Site
Trumbull Connecticut, 06611, United States
Novartis Investigative Site
Rockville Maryland, 20850, United States
Novartis Investigative Site
Andover Massachusetts, 01810, United States
Novartis Investigative Site
Boston Massachusetts, 02114, United States
Novartis Investigative Site
Troy Michigan, 48084, United States
Novartis Investigative Site
East Windsor New Jersey, 08520, United States
Novartis Investigative Site
New York New York, 10025, United States
Novartis Investigative Site
New York New York, 10075, United States
Novartis Investigative Site
Winston-Salem North Carolina, 27157, United States
Novartis Investigative Site
Gahanna Ohio, 43230, United States
Novartis Investigative Site
Hershey Pennsylvania, 17033, United States
Novartis Investigative Site
Pittsburgh Pennsylvania, 15213, United States
Novartis Investigative Site
Arlington Texas, 76011, United States
Novartis Investigative Site
Salt Lake City Utah, 84132, United States
Novartis Investigative Site
West Jordan Utah, 84088, United States

How clear is this clinincal trial information?

Study is for people with:

Psoriasis

Phase:

Phase 3

Estimated Enrollment:

102

Study ID:

NCT02267135

Recruitment Status:

Completed

Sponsor:


Novartis Pharmaceuticals

How clear is this clinincal trial information?

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