Eli Lilly Reports Results of Olumiant (baricitinib) in P-III BREEZE-AD1 and BREEZE-AD2 study for Moderate-to-Severe Atopic Dermatitis (AD)

 Eli Lilly Reports Results of Olumiant (baricitinib) in P-III BREEZE-AD1 and BREEZE-AD2 study for Moderate-to-Severe Atopic Dermatitis (AD)

Eli Lilly Reports Results of Olumiant (baricitinib) in P-III BREEZE-AD1 and BREEZE-AD2 study for Moderate-to-Severe Atopic Dermatitis (AD)

Shots:

  • The two P-III study BREEZE-AD1 and BREEZE-AD2 involves assessing of baricitinib vs PBO in patients with moderate-to-severe AD
  • The two P-III study resulted in meeting 1EPs @16 wks. with no venous thromboembolic events (VTEs), major adverse cardiovascular events (MACE) & deaths rates
  • Olumiant (baricitinib, 2mg) indicated for moderate-to-severe RA who have had an inadequate response to TNF antagonist therapies and is approved in 50 countries including the US, EU, and Japan. In Dec,2009 Lilly and Incyte collaborated to develop and commercialize baricitinib for inflammatory and autoimmune diseases

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