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Drug Overview: lumateperone

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    Report

  • 25 Pages
  • April 2018
  • Region: Global
  • Citeline
  • ID: 4533523
Drug Overview

Lumateperone is a novel, orally available antipsychotic being developed by Intra-Cellular Therapies for several neuropsychiatric disorders. Lumateperone acts as a serotonin 5-HT2A receptor antagonist, a modulator of the dopaminergic and glutamatergic systems, and a serotonin reuptake inhibitor. By targeting the serotonergic and dopaminergic systems, the drug appears to reduce agitation and minimize positive symptoms. Its additional actions on glutamatergic signaling are believed to help address both negative and cognitive schizophrenia symptoms.

Intra-Cellular Therapies licensed lumateperone from its original developer, Bristol-Myers Squibb, in 2005, and is now solely responsible for the drug’s development. In December 2015, the company announced the initiation of patient enrollment for its two Phase III trials in bipolar depression. Additional clinical programs with lumateperone include its Phase III development in schizophrenia and behavioral disturbances in dementia.

Table of Contents

OVERVIEW
Drug Overview
Product Profiles
lumateperone: Bipolar disorder
lumateperone: Schizophrenia

List of Figures
Figure 1: Lumateperone for bipolar disorder - SWOT analysis
Figure 2: Drug assessment summary for lumateperone in bipolar disorder
Figure 3: Drug assessment summary for lumateperone in bipolar disorder
Figure 4: Lumateperone for schizophrenia - SWOT analysis
Figure 5: Drug assessment summary of lumateperone for schizophrenia
Figure 6: Drug assessment summary of lumateperone for schizophrenia
Figure 7: Lumateperone sales for schizophrenia in the US, 2017-26

List of Tables
Table 1: Lumateperone drug profile
Table 2: Lumateperone Phase III trials in bipolar disorder
Table 3: Lumateperone drug profile
Table 4: Lumateperone Phase II and Phase III data in schizophrenia
Table 5: Lumateperone other interim Phase II data in schizophrenia
Table 6: Lumateperone sales for schizophrenia in the US ($m), 2017-26