The Lupus Research Alliance is pleased to share good news about a potential new treatment for systemic lupus erythematosus (SLE).
NEW YORK, /PRNewswire/ -- The Lupus Research Alliance is pleased to share good news about a potential new treatment for systemic lupus erythematosus (SLE). Today, Eli Lilly and Company and Incyte Corporation announced that the U.S. Food and Drug Administration (FDA) granted Fast Track designation to baricitinib, which is being studied for the treatment of SLE. The FDA describes Fast Track designation as: “a process designed to facilitate the development and expedite the review of drugs to treat serious conditions and fill an unmet medical need.” This designation was informed by positive results of a Phase 2 study of baricitinib for the treatment of SLE presented at the European Congress of Rheumatology (EULAR) and published by The Lancet. Lilly is currently conducting two Phase 3 SLE trials to test two doses of baricitinib. Baricitinib is currently approved in the U.S. and 50 countries throughout the world as a treatment for rheumatoid arthritis under the brand name OLUMIANT®. “We are watching baricitinib development closely and applaud this latest milestone,” noted Lupus Research Alliance Research Director, Dr. Teodora Staeva. “Additional treatment options are urgently needed for lupus, and our mission is to support research that brings us closer to improved care as well as long-term prevention and a cure.” About Lupus About the Lupus Research Alliance View original content:http://www.prnewswire.com/news-releases/lupus-research-alliance-applauds-fdas-fast-track-designation-to-develop-baricitinib-for-lupus-300765780.html SOURCE Lupus Research Alliance |