COSENTYX (secukinumab) by Novartis is interleukin-17a antagonists [moa]. Approved for interleukin-17a antagonist [epc]. First approved in 2023.
Drug data last refreshed 11h ago · AI intelligence enriched 1w ago
COSENTYX (secukinumab) is a fully human monoclonal antibody that selectively targets and inhibits interleukin-17A, a key cytokine in inflammatory and autoimmune disease pathways. It is approved for multiple indications including plaque psoriasis, psoriatic arthritis, ankylosing spondylitis, and other IL-17A-driven conditions. The drug works by blocking IL-17A signaling, thereby reducing inflammatory responses in affected tissues.
COSENTYX is in active growth phase with moderate competitive pressure (30%), signaling expanding team investments and revenue-generation opportunities in commercial and medical affairs.
Interleukin-17A Antagonists
Interleukin-17A Antagonist
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
A Study of Early Secukinumab Treatment in Moderate to Severe Hidradenitis Suppurativa Patients
A Study to Assess the Safety of Subcutaneous Secukinumab for Treatment in Adult Indian Participants With Axial Spondyloarthritis (axSpA), Ankylosing Spondylitis (AS), and Non-Radiographic Axial Spondyloarthritis (nr-axSpA)
A Real-world Study of Patients With Hidradenitis Suppurativa and High Cardiovascular Risk or Established Coronary Plaque Treated With Secukinumab
A Study to Estimate Secukinumab Retention Rate in Psoriasis Patients With MASLD
Study of Efficacy and Safety of Secukinumab in Chinese Adult Patients With Moderate to Severe Hidradenitis Suppurativa
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The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.
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Upgrade to Pro — $25/moWorking on COSENTYX positions professionals in a high-growth biologics product with established market validation and competitive dynamics. The growth-phase lifecycle and moderate competitive pressure indicate stable budgets, team expansion, and opportunities for career advancement in both commercial and medical functions.