Emmaus Life Sciences Announces SFDA (Saudi Food & Drug Authority) Accepts Endari® Priority Review Request
EMMAUS LIFE SCIENCES INC (EMMA)
Company Research
Source: GlobeNewswire
TORRANCE, Calif., April 16, 2020 (GLOBE NEWSWIRE) -- Emmaus Life Sciences, Inc. (OTCQB: EMMA), a leader in sickle cell disease treatment, announced today that the SFDA (Saudi Food & Drug Authority) has accepted its request for priority review of Endari®, its prescription grade L-glutamine oral powder. Similar to the U.S. Food & Drug Administration (FDA), priority review by the SFDA in Saudi Arabia is a program designated to expedite the review process for drugs that are expected to have a particularly significant positive impact on the treatment of a disease. Saudi Arabia has the highest prevalence of sickle cell disease in the MENA (Middle East, North Africa) region. Emmaus estimates that there are approximately 225,000 sickle cell disease patients that could potentially be treated with Endari® in that region. Yutaka Niihara, M.D., M.P.H., Chairman and Chief Executive Officer of Emmaus, stated, “We are pleased that the SFDA has accepted our priority review request for Endari®. E
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