SOTYKTU (deucravacitinib) by Bristol Myers Squibb is tyrosine kinase 2 inhibitors [moa]. First approved in 2022.
Drug data last refreshed 13h ago · AI intelligence enriched Yesterday
SOTYKTU (deucravacitinib) is an oral tyrosine kinase 2 inhibitor approved in September 2022 by Bristol Myers Squibb. It represents a targeted small-molecule approach to modulating immune-mediated inflammatory pathways through selective TYK2 inhibition.
Product is in peak commercialization phase with ~$34M Part D spending in 2023; Medical Affairs team expansion likely underway to support peak market penetration.
Tyrosine Kinase 2 Inhibitors
Tyrosine Kinase 2 Inhibitor
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Continued Access to Deucravacitinib for Adult SLE/SjD and Pediatric PsO/PsA Study Completers
Deucravacitinib in the Treatment of Cicatricial Alopecias
A Study to Continue the Administration of Deucravacitinib in Participants With Systemic Lupus Erythematosus (SLE) or Discoid and/or Subacute Cutaneous Lupus Erythematosus (DLE/SCLE) Who Have Completed Study IM011074 or Study IM011132
A Study to Evaluate the Efficacy, Safety, and Drug Levels of Deucravacitinib (BMS-986165) in Adolescent Participants With Moderate to Severe Plaque Psoriasis
Long-Term Safety Study of Deucravacitinib Versus Ustekinumab in Participants With Psoriasis (PRAGMATYK)
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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/moBristol Myers Squibb is hiring 4 roles related to this product
Working on SOTYKTU offers focused opportunities in Medical Affairs and leadership roles, with a small but specialized job market reflecting the product's targeted commercial footprint. The peak lifecycle stage suggests stability but limited growth in headcount compared to launch-phase products.
3 open roles linked to this drug