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A double-blind, placebo-controlled comparator study of LY2140023 monohydrate in patients with schizophrenia
BACKGROUND: Pomaglumetad methionil (LY2140023 monohydrate) is a potent and highly selective agonist for the metabotropic glutamate mGluR2 and mGluR3 receptors. We present results of a pivotal clinical study H8Y-MC-HBBM assessing the efficacy of LY2140023 in improving symptoms as a monotherapy in pat...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4276262/ https://www.ncbi.nlm.nih.gov/pubmed/25539791 http://dx.doi.org/10.1186/s12888-014-0351-3 |
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author | Downing, AnnCatherine M Kinon, Bruce J Millen, Brian A Zhang, Lu Liu, Lin Morozova, Margarita A Brenner, Ronald Rayle, Tami Jo Nisenbaum, Laura Zhao, Fangyi Gomez, Juan Carlos |
author_facet | Downing, AnnCatherine M Kinon, Bruce J Millen, Brian A Zhang, Lu Liu, Lin Morozova, Margarita A Brenner, Ronald Rayle, Tami Jo Nisenbaum, Laura Zhao, Fangyi Gomez, Juan Carlos |
author_sort | Downing, AnnCatherine M |
collection | PubMed |
description | BACKGROUND: Pomaglumetad methionil (LY2140023 monohydrate) is a potent and highly selective agonist for the metabotropic glutamate mGluR2 and mGluR3 receptors. We present results of a pivotal clinical study H8Y-MC-HBBM assessing the efficacy of LY2140023 in improving symptoms as a monotherapy in patients with an acute exacerbation of schizophrenia. METHODS: Enrolled adult patients (ages 18–65) with schizophrenia who had experienced an exacerbation of symptoms within 2 weeks prior to study entry. Patients (N = 1013) were randomized 2:2:2:1 to treatment with placebo, LY40 mg twice daily (BID), LY80 mg BID, or risperidone (RIS) 2 mg BID for 6 weeks after a one-week blinded placebo lead-in. The primary outcome assessed change from baseline in the Positive and Negative Syndrome Scale (PANSS) total score in an overall schizophrenia population and a predefined subpopulation which excluded non-Hispanic white patients with the A/A genotype at the HTR2A SNP rs7330461. RESULTS: Neither LY2140023 dose showed significant improvement compared to placebo on PANSS total in either population (1-sided p-value [significance level], overall: LY40, p = .154 [0.01]; LY80, p = .698 [0.01], subpopulation: LY40, p = .033 [0.0025]; LY80, p = .659 [0.0025], MMRM analysis). RIS statistically separated from placebo in both populations (p < .001 [0.05]). There were no statistically significant differences in the incidence of serious adverse events, and no seizures on LY2140023. CONCLUSION: LY2140023 treatment did not demonstrate efficacy in populations studied. Overall, LY2140023 treatment was generally well tolerated with no new adverse safety findings compared to previous trials. Further understanding of the role of glutamate as a therapeutic target in schizophrenia is needed. CLINICAL TRIALS REGISTRATION: A Phase 2, Multicenter, Double-Blind, Placebo-Controlled Comparator Study of 2 Doses of LY2140023 Versus Placebo in Patients With DSM-IV-TR Schizophrenia ClinicalTrials.gov identifier: NCT01086748. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12888-014-0351-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4276262 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42762622014-12-25 A double-blind, placebo-controlled comparator study of LY2140023 monohydrate in patients with schizophrenia Downing, AnnCatherine M Kinon, Bruce J Millen, Brian A Zhang, Lu Liu, Lin Morozova, Margarita A Brenner, Ronald Rayle, Tami Jo Nisenbaum, Laura Zhao, Fangyi Gomez, Juan Carlos BMC Psychiatry Research Article BACKGROUND: Pomaglumetad methionil (LY2140023 monohydrate) is a potent and highly selective agonist for the metabotropic glutamate mGluR2 and mGluR3 receptors. We present results of a pivotal clinical study H8Y-MC-HBBM assessing the efficacy of LY2140023 in improving symptoms as a monotherapy in patients with an acute exacerbation of schizophrenia. METHODS: Enrolled adult patients (ages 18–65) with schizophrenia who had experienced an exacerbation of symptoms within 2 weeks prior to study entry. Patients (N = 1013) were randomized 2:2:2:1 to treatment with placebo, LY40 mg twice daily (BID), LY80 mg BID, or risperidone (RIS) 2 mg BID for 6 weeks after a one-week blinded placebo lead-in. The primary outcome assessed change from baseline in the Positive and Negative Syndrome Scale (PANSS) total score in an overall schizophrenia population and a predefined subpopulation which excluded non-Hispanic white patients with the A/A genotype at the HTR2A SNP rs7330461. RESULTS: Neither LY2140023 dose showed significant improvement compared to placebo on PANSS total in either population (1-sided p-value [significance level], overall: LY40, p = .154 [0.01]; LY80, p = .698 [0.01], subpopulation: LY40, p = .033 [0.0025]; LY80, p = .659 [0.0025], MMRM analysis). RIS statistically separated from placebo in both populations (p < .001 [0.05]). There were no statistically significant differences in the incidence of serious adverse events, and no seizures on LY2140023. CONCLUSION: LY2140023 treatment did not demonstrate efficacy in populations studied. Overall, LY2140023 treatment was generally well tolerated with no new adverse safety findings compared to previous trials. Further understanding of the role of glutamate as a therapeutic target in schizophrenia is needed. CLINICAL TRIALS REGISTRATION: A Phase 2, Multicenter, Double-Blind, Placebo-Controlled Comparator Study of 2 Doses of LY2140023 Versus Placebo in Patients With DSM-IV-TR Schizophrenia ClinicalTrials.gov identifier: NCT01086748. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12888-014-0351-3) contains supplementary material, which is available to authorized users. BioMed Central 2014-12-10 /pmc/articles/PMC4276262/ /pubmed/25539791 http://dx.doi.org/10.1186/s12888-014-0351-3 Text en © Downing et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Downing, AnnCatherine M Kinon, Bruce J Millen, Brian A Zhang, Lu Liu, Lin Morozova, Margarita A Brenner, Ronald Rayle, Tami Jo Nisenbaum, Laura Zhao, Fangyi Gomez, Juan Carlos A double-blind, placebo-controlled comparator study of LY2140023 monohydrate in patients with schizophrenia |
title | A double-blind, placebo-controlled comparator study of LY2140023 monohydrate in patients with schizophrenia |
title_full | A double-blind, placebo-controlled comparator study of LY2140023 monohydrate in patients with schizophrenia |
title_fullStr | A double-blind, placebo-controlled comparator study of LY2140023 monohydrate in patients with schizophrenia |
title_full_unstemmed | A double-blind, placebo-controlled comparator study of LY2140023 monohydrate in patients with schizophrenia |
title_short | A double-blind, placebo-controlled comparator study of LY2140023 monohydrate in patients with schizophrenia |
title_sort | double-blind, placebo-controlled comparator study of ly2140023 monohydrate in patients with schizophrenia |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4276262/ https://www.ncbi.nlm.nih.gov/pubmed/25539791 http://dx.doi.org/10.1186/s12888-014-0351-3 |
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