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Updated as of October 31, 2023

Please refer to local prescribing information for more information, including full safety information, on Incyte’s marketed medicines, or on medicines marketed by Incyte’s collaboration partners.  

1. Marketed by Incyte in the U.S.; ruxolitinib licensed to Novartis outside the U.S. 2. Approved in the U.S. 3. In collaboration with Syndax    
4. Approved in multiple territories, including the U.S., Canada, Europe, and Japan  5. Approved in Japan 6. Development in collaboration with MorphoSys and co-commercialization in the U.S. with MorphoSys; exclusive commercialization rights held by Incyte outside the U.S.
7. Approved in Europe 8. Approved in Canada 9. European rights to Iclusig licensed from Takeda 10. Licensed from MacroGenics 11. Discovery collaboration with Agenus 12. Development in collaboration with Merus 13. Worldwide rights to baricitinib licensed to Lilly  14. Approved in multiple territories globally 15. Worldwide rights to capmatinib licensed to Novartis

1L, first-line; 2L+, second-line or later; AD, atopic dermatitis; ALL, acute lymphoblastic leukemia; DLBCL, diffuse large B-cell lymphoma; FGFR, fibroblast growth factor receptor; GVHD, graft-versus-host disease; IAI, inflammation and autoimmunity; mAb, monoclonal antibody; MF, myelofibrosis; MLNs, myeloid/lymphoid neoplasms; MPNs, myeloproliferative neoplasms; MSI-H, microsatellite instability-high; MZL, marginal zone lymphoma; NSCLC, non-small cell lung cancer; Ph+, Philadelphia chromosome-positive; QD, once daily; r/r, relapsed or refractory; XR, extended release.