Cosentyx® (secukinumab)

BL 125504

Cosentyx® (secukinumab)

BL 125504

U.S. License Holder:

Novartis Pharms. Corp.

Date of License:

January-21-2015

Last Update:

November-23-2020

approved_indications FDA-Approved Indications

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

Moderate to severe plaque psoriasis in adult patients who are candidates for systemic therapy or phototherapy;

Adults with active psoriatic arthritis (PsA);

Adults with active ankylosing spondylitis (AS);

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

Methodology

Information contained in the Venable Fitzpatrick 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 Fitzpatrick BiologicsHQ database.

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