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Lancet 2021

While one study did show statistical significance, the FDA said in a Complete Response Letter that it was insufficient on its own [to provide] substantial evidence of effectiveness. The FDA also noted that the NDA submission lacked data on concomitant antipsychotic administration, did not include data that established that the change in negative symptoms was clinically meaningful and that the submitted safety database had an inadequate number of subjects exposed to roluperidone at the proposed dose of 64 mg for at least 12 months

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It is suitable for all skin types, including sensitive and mature skin

Food and Drug Administration (FDA) nod to treat obesity two years ago

Benefits may include improved sleep quality, faster recovery, better body composition, increased energy, and enhanced fat metabolism