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NRx Pharmaceuticals announces patient data on RWE on ketamine submitted to FDA

NRx Pharmaceuticals (NRXP) announced that it has licensed Real World Evidence, RWE, drawn from over 70,000 patients in the United States who were treated with either intravenous ketamine or nasal S-ketamine for depression and suicidal ideation. The information is being submitted in support of NRx’s application for Accelerated Approval of NRX-100 under Fast Track Designation for Treatment of Suicidal Ideation in Depression and Bipolar Depression. Currently, there is no medicine approved to treat suicidal ideation and the only FDA-approved treatment today is Electroshock Therapy.

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