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The phase 2 clinical trial used a starting dose of 2 mg, increasing every four weeks through 4 mg, 6 mg, 8 mg, and potentially up to 12 mg depending on the treatment arm

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, markedly less damaged neurons in most severely injuried areas) is in accord with: its neuroprotective properties (22, 34), consistent antagonization of different central disturbances (16-23, 34), brain 5-HT synthesis and antagonization of serotonin-syndrome in rats based on region-specific influence on the brain given peripherally either acutely or chronically ( i.e

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