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Eli Lilly's Olumiant (baricitinib) Receives FDA's Fast Track Designation for Systemic Lupus Erythematosus (SLE)

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Eli Lilly's Olumiant (baricitinib) Receives FDA's Fast Track Designation for Systemic Lupus Erythematosus (SLE)

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  • The FDA’s designation is based on P-II study results assessing Baricitinib in patients with SLE- presented at European Congress of Rheumatology 2018
  • Lilly is also evaluating baricitinib’s two doses in P-III SLE trials and for moderate-to -severe atopic dermatitis- with its expected results in H1’19
  • Olumiant (baricitinib) 2mg is an inhibitor of janus kinase- further blocking its subtypes JAK1 and JAK2 and is approved in 50 countries for adults with rheumatoid arthritis

  Ref: Eli Lilly | Image:  Eli Lilly


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