APCER Report Confirms Endari® Safety
EMMAUS LIFE SCIENCES INC (EMMA)
Company Research
Source: GlobeNewswire
TORRANCE, Calif., April 27, 2020 (GLOBE NEWSWIRE) -- Emmaus Life Sciences, Inc. (OTCQB: EMMA), a leader in sickle cell disease treatment, announced today that APCER Life Sciences (APCER) has confirmed the safety profile of Endari®, Emmaus’ prescription grade L-glutamine oral powder for the treatment of sickle cell disease. Using the signal detection method to identify adverse drug reactions (ADR), APCER indicated that no serious safety concerns were reported among patients using Endari® during the period from July 7, 2017 to April 6, 2020. See https://ir.emmausmedical.com/company-information/presentations. Yutaka Niihara, M.D., M.P.H., Chairman and Chief Executive Officer of Emmaus, stated, “We are pleased that the APCER report has reconfirmed the safety profile found in the clinical trials where there were no serious ADRs attributable to Endari. Since its approval by the FDA in July 2017, there have been approximately 20,000 prescriptions written for Endari and it is significant t
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