Cosentyx® (secukinumab)

BL 125504 [BL 761349]

Cosentyx® (secukinumab)

BL 125504 [BL 761349]

U.S. License Holder:

Novartis Pharms. Corp.

Date of License:

January-21-2015 [October-06-2023]

Last Update:

June-23-2025

approved_indications FDA-Approved Indications

COSENTYX (secukinumab) is a human interleukin-17A antagonist indicated for the treatment of:

Moderate to severe plaque psoriasis (PsO) in patients 6 years and older who are candidates for systemic therapy or phototherapy;

Active psoriatic arthritis (PsA) in patients 2 years of age and older;

Adults with active ankylosing spondylitis (AS);

Adults with active non-radiographic axial spondyloarthritis (nr-axSpA) with objective signs of inflammation;

Active enthesitis-related arthritis (ERA) in pediatric patients 4 years of age and older;

Adults with moderate to severe hidradenitis suppurativa (HS).

Methodology

Information contained in the Venable BiologicsHQ database relates to FDA-approved drug products listed in the CDER Purple Book or on the FDA website (www.fda.gov). Information relating to FDA licensed products, FDA-approved indications, and aBLA and 505(b)(2) applications is obtained from public sources including the U.S. FDA website (www.fda.gov). Information relating to litigations is given only for cases active from January 31, 2010 onward. Information relating to foreign biosimilar / biologics follow-on products approved in Australia, Canada, the E.U., Japan and South Korea is from public sources. Statistics graphics are compiled from information contained in the Venable BiologicsHQ database.

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