FDA Approves L-Glutamine Powder for the Treatment of Sickle Cell Disease

U.S. Food and Drug Administration
Voice

Description

On July 7, 2017, the U.S. Food and Drug Administration (FDA) 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 five years and older.

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