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Iloperidone: a new option for the treatment of schizophrenia.

Abstract
Schizophrenia is a debilitating condition associated with high morbidity and mortality. While currently available atypical antipsychotic agents have significantly advanced the treatment of schizophrenia, there is still a great unmet need for new, effective and better-tolerated therapies. Iloperidone, a D(2)/5-HT(2) receptor antagonist, has been recently approved by the US FDA for the acute treatment of schizophrenia in adults. Iloperidone has been shown to be effective in the treatment of schizophrenia in four short-term (4-6 weeks) and three long-term (52 weeks) studies with over 3000 patients exposed to treatment. Results also indicated a reassuring safety profile, particularly regarding extrapyramidal symptoms, akathisia and prolactin elevation, with a modest effect on weight gain and no medically important changes in cholesterol, triglycerides and glucose. As other antipsychotics, iloperidone has been shown to prolong the QTc interval. Since none of the current therapies work for every patient, a pharmacogenetic approach was used to identify genetic markers associated with increased response to iloperidone, suggesting a personalized therapeutic option for this drug. In addition, a long-term 4-week injectable formulation is being developed that may assist with patient compliance. Key development findings for iloperidone are presented here.
AuthorsAndrew J Cutler
JournalExpert review of neurotherapeutics (Expert Rev Neurother) Vol. 9 Issue 12 Pg. 1727-41 (Dec 2009) ISSN: 1744-8360 [Electronic] England
PMID19951132 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)
Chemical References
  • Antipsychotic Agents
  • Isoxazoles
  • Piperidines
  • iloperidone
Topics
  • Antipsychotic Agents (chemistry, therapeutic use)
  • Brief Psychiatric Rating Scale
  • Clinical Trials as Topic
  • Confidence Intervals
  • Humans
  • Isoxazoles (chemistry, therapeutic use)
  • Kaplan-Meier Estimate
  • Longitudinal Studies
  • Piperidines (chemistry, therapeutic use)
  • Schizophrenia (drug therapy, metabolism, mortality, physiopathology)

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