FDA approved L-glutamine powder for the treatment of sickle cell disease – Katalyst HLS


On July 7, 2017, the U.S. Food and Drug Administration approved L-glutamine oral powder (Endari, Emmaus Medical, Inc.) for oral administration to reduce the acute complications of sickle cell disease in adult and pediatric patients 5 years and older.
@Katalyst HealthCares & Life Sciences Inc.,
https://www.fda.gov/Drugs/InformationOnDrugs/ApprovedDrugs/ucm566097.htm

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