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FDA Purple Book · Reference family

secukinumab (Cosentyx)

secukinumab is an FDA-licensed reference biologic from Novartis Pharmaceuticals Corporation. Reference exclusivity, biosimilar lineage, and published patents from official FDA Purple Book records.

0

Biosimilars

0

Interchangeables

0

Listed patents

2021

Reference approved

Reference product

351(a)BLA 125504

Cosentyx secukinumab

Novartis Pharmaceuticals Corporation

Approved
May 28, 2021
Marketing
Rx
Center
CDER
Patents
None listed

Molecular structure

Experimental 3D structure for secukinumab from the RCSB Protein Data Bank (PDB 9SFX).

3D molecular structure of secukinumab (PDB entry 9SFX)

Interactive biological assembly from PDB entry 9SFX. Drag to rotate, scroll to zoom, and inspect the full atomic structure right here — no need to leave the page.

Exclusivity & patent cliffs

Approval, exclusivity, and published-patent expiration dates for secukinumab, in chronological order.

  1. Reference approval

    Approval date of the reference secukinumab product.

    5 yr 1 mo ago

Frequently asked questions

Are there biosimilars approved for secukinumab (Cosentyx)?

No 351(k) biosimilars or interchangeable biosimilars referencing secukinumab are listed in the FDA Purple Book yet.

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