Wezlana (ustekinumab-auub)

aBL 761285 / aBL 761331

Wezlana (ustekinumab-auub)

aBL 761285 / aBL 761331

U.S. License Holder:

Amgen, Inc.

Date of License:

October-31-2023 (Interchangeable)

Last Update:

Nov-15-2024

approved_indications FDA-Approved Indications

WEZLANA (ustekinumab-auub) is a human interleukin -12 and -23 antagonist indicated for the treatment of:

Adult patients with:

Moderate to severe plaque psoriasis (Ps) who are candidates for phototherapy or systemic therapy;

Active psoriatic arthritis (PsA);

Moderately to severely active Crohn's disease (CD);

Moderately to severely active ulcerative colitis.

Pediatric patients 6 years and older with:

Moderate to severe plaque psoriasis, who are candidates for phototherapy or systemic therapy;

Active psoriatic arthritis (PsA).

approved_indications Approved Foreign Follow-On Biologics / Biosimilars

Biosimilars Approved In Canada

Wezlana (Amgen) (December-2023)

Biosimilars Approved In The E.U.

Wezenla (Amgen) (June-2024)

Biosimilars Approved In Australia

Wezlana (Amgen) (January-2024)

approved_indications U.S. Patent Litigations

PACER

Case No(s):

1:22-cv-01549 (D. Del.)

U.S. Patent Nos.
6,902,734 (Anti-IL-12 Antibodies and Compositions Thereof) 8,852,889 (Cell Culture Process) 9,217,168 (Methods of Cell Culture) 9,475,858 (Cell Culture Process) 9,663,810 (Methods of Cell Culture) 10,961,307 (Methods of Treating Moderately to Severely Active Ulcerative Colitis by Administering an Anti-IL12/IL23 Antibody)

Plaintiffs
Janssen Biotech, Inc.

Defendants
Amgen, Inc.

Status
Stipulated Dismissal Due to Settlement

BPCIA
Y

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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