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Cosentyx® (secukinumab)

Cosentyx is indicated for the treatment of moderate to severe plaque psoriasis (PsO) in adults, children and adolescents from the age of 6 years who are candidates for systemic therapy; active psoriatic arthritis (PsA) in adult patients (alone or in combination with methotrexate [MTX]) when the response to previous disease-modifying anti-rheumatic drug therapy has been inadequate; active ankylosing spondylitis (AS) in adults who have responded inadequately to conventional therapy; active non-radiographic axial spondyloarthritis (nr-axSpA) with objective signs of inflammation as indicated by elevated C-reactive protein and/or magnetic resonance imaging evidence in adults who have responded inadequately to non-steroidal anti-inflammatory drugs; active moderate to severe hidradenitis suppurativa (HS; acne inversa) in adults with an inadequate response to conventional systemic HS therapy; active enthesitis-related arthritis (ERA) in patients 6 years and older (alone or in combination with MTX) whose disease has responded inadequately to, or who cannot tolerate, conventional therapy; active juvenile psoriatic arthritis (JPsA) in patients 6 years and older (alone or in combination with MTX) whose disease has responded inadequately to, or who cannot tolerate, conventional therapy.1

Cosentyx is intended for use under the guidance and supervision of a physician experienced in the diagnosis and treatment of conditions for which Cosentyx is indicated.1

In Ireland Cosentyx is reimbursed for the following indications: adult plaque psoriasis (PsO); psoriatic arthritis (PsA) and axial spondyloarthritis (axSpA).

Please refer to the Summary of Product Characteristics (SmPC) for full prescribing information and safety profile.1


Cosentyx is the FIRST biologic with proven efficacy in all six manifestations1–7

Key clinical manifestations of PsA are joint, axial, skin, enthesitis, dactylitis and nails.5

Joints

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Circular image of an elbow.

68%

achieved ACR50 
at Year 1 in ULTIMATE*6

Skin

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Circular image of a person's skin with PsO.

74%

maintained PASI 90 
at Year 5 in FUTURE 2†3

Nails

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Circular image of a person's foot and toe nails.

–73%

observed improvement from baseline in mNAPSI 
at 2.5 years in TRANSFIGURE‡7

Axial

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Circular image of a person's back.

69%

sustained ASAS40
at Year 1 in MAXIMISE§5

Dactylitis

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Circular image of a person's thumbs.

94%

achieved resolution 
at Year 5 in FUTURE 2¶3

Enthesitis

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Circular image of a pair of ankles.

83%

achieved resolution 
at Year 5 in FUTURE 2‖3

All the primary endpoints were met in the studies referenced above.3,5–7



Cosentyx is intended for use under the guidance and supervision of a physician experienced in the diagnosis and treatment of conditions for which Cosentyx is indicated. Please refer to the Cosentyx SmPC for full product information before prescribing.1

*ULTIMATE: Observed data in biologic-naïve patients with PsA receiving Cosentyx 300 mg or 150 mg who were originally randomly assigned to Cosentyx (n=83).6
FUTURE 2: Observed data for the 150-mg treatment group of biologic-naïve patients with PsO affecting 3% or more of body surface area at baseline including those originally randomly assigned to Cosentyx and placebo-switchers (n=42); 64% in the respective 300-mg group maintained PASI 90 through Year 5 (n=28).3
TRANSFIGURE: Observed data in patients with moderate to severe nail PsO in the Cosentyx 300 mg treatment group (n=66; NRI; observed data).7
§MAXIMISE: Observed data in biologic-naïve patients with PsA in the Cosentyx 300 mg treatment group (n=139); in the respective Cosentyx 150 mg treatment group, 65% achieved ASAS40 at Year 1 (n=141).5
FUTURE 2: Observed data for the Cosentyx 300 mg treatment group of biologic-naïve patients with this symptom at baseline, including those originally randomly assigned to Cosentyx and placebo-switchers (n=31); 86% in the respective Cosentyx 150 mg group maintained complete resolution of dactylitis through Year 5 (n=22).3
FUTURE 2: Observed data for the Cosentyx 300 mg treatment group of biologic-naïve patients with this symptom at baseline, including those originally randomly assigned to Cosentyx and placebo-switchers (n=36); 76% in the respective Cosentyx 150 mg group maintained complete resolution of enthesitis through Year 5 (n=45).3

ACR, American College of Rheumatology; AS, ankylosing spondylitis; ASAS, Assessment of Spondyloarthritis International Society; axSpA, axial spondyloarthritis; ERA, enthesitis-related arthritis; HS, hidradenitis suppurativa; JIA, juvenile idiopathic arthritis; JPsA, juvenile psoriatic arthritis; mNAPSI, modified nail psoriasis severity index; MTX, methotrexate; nr-axSpA, non-radiographic axial spondyloarthritis; NRI, non-responder imputation; PASI, psoriasis area and severity index; PsA, psoriatic arthritis; PsO, plaque psoriasis; SmPC,summary of product characteristics.

References

  1. Cosentyx® (secukinumab) Summary of Product Characteristics. Available at www.medicines.ie.

  2. Baraliakos X, et al. Ann Rheum Dis 2020;0:1–9.

  3. McInnes IB, et al. Lancet Rheumatol 2020;2(4):e227-e235 and supplementary appendix.

  4. Mease PJ, et al. ACR Open Rheumatol 2020 Jan;2(1):18–25.

  5. Baraliakos X, et al. Ann Rheum Dis 2021;80(5):582–590.

  6. D’Agostino MA, et al. Semin Arthritis Rheum 2023;63:152259 and supplementary appendix.

  7. Reich K, et al. Br J Dermatol 2021;184(3):425–436.

IE11533962 | March 2026

Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk profile of the medicinal product. All suspected adverse reactions should be reported to HPRA Pharmacovigilance at www.hpra.ie. Adverse events can also be reported to Novartis preferably at www.novartis.com/report, by emailing [email protected] or by calling (01) 2080 612.