myTomorrows and Emmaus Life Sciences, Inc. announced the availability of an Early Access Program for pharmaceutical grade L-Glutamine (oral powder) for the treatment of Sickle Cell Disease patients that have exhausted other remaining treatment options. This Early Access Program, currently run on a named patient basis, provides physicians in the EU, Turkey, Middle-east and South America with the possibility to prescribe L-Glutamine to eligible patients prior to authorization. L-Glutamine was approved in the US on 7 July 2017 under the trade name Endari™ for the treatment of Sickle Cell Disease in adult and paediatric patients 5 years of age and older. On 11 December 2017, at the 59th Annual Meeting of the American Society of Hematology (ASH) in Atlanta, Georgia, Emmaus announced the availability of L-Glutamine for treatment of Sickle Cell Disease patients in the US.