Cargando…

An Evidence-Based Review of OLZ/SAM for Treatment of Adults with Schizophrenia or Bipolar I Disorder

Olanzapine effectively treats schizophrenia and bipolar I disorder (BD-I); however, its use is limited by the risk of significant weight gain and metabolic effects. OLZ/SAM, a combination of olanzapine and samidorphan, was recently approved in the United States for the treatment of adults with schiz...

Descripción completa

Detalles Bibliográficos
Autores principales: Citrome, Leslie, Graham, Christine, Simmons, Adam, Jiang, Ying, Todtenkopf, Mark S, Silverman, Bernard, DiPetrillo, Lauren, Cummings, Hannah, Sun, Lei, McDonnell, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8437420/
https://www.ncbi.nlm.nih.gov/pubmed/34526769
http://dx.doi.org/10.2147/NDT.S313840
_version_ 1783752163978117120
author Citrome, Leslie
Graham, Christine
Simmons, Adam
Jiang, Ying
Todtenkopf, Mark S
Silverman, Bernard
DiPetrillo, Lauren
Cummings, Hannah
Sun, Lei
McDonnell, David
author_facet Citrome, Leslie
Graham, Christine
Simmons, Adam
Jiang, Ying
Todtenkopf, Mark S
Silverman, Bernard
DiPetrillo, Lauren
Cummings, Hannah
Sun, Lei
McDonnell, David
author_sort Citrome, Leslie
collection PubMed
description Olanzapine effectively treats schizophrenia and bipolar I disorder (BD-I); however, its use is limited by the risk of significant weight gain and metabolic effects. OLZ/SAM, a combination of olanzapine and samidorphan, was recently approved in the United States for the treatment of adults with schizophrenia or BD-I. OLZ/SAM provides the efficacy of olanzapine while mitigating olanzapine-associated weight gain through opioid-receptor blockade. Here, we summarize OLZ/SAM clinical data characterizing pharmacokinetics, antipsychotic efficacy, weight mitigation efficacy, safety, and long-term treatment effects. In an acute exacerbation of schizophrenia, OLZ/SAM and olanzapine provided similar symptom improvements versus placebo at week 4. In stable outpatients with schizophrenia, OLZ/SAM treatment resulted in significantly less weight gain, reducing the risk for clinically significant weight gain and waist circumference increases of ≥5 cm by half, compared with olanzapine at week 24. Based on open-label extension studies, OLZ/SAM is safe and well tolerated for up to 3.5 years of treatment, while maintaining schizophrenia symptom control and stabilizing weight. The olanzapine component of OLZ/SAM was bioequivalent to branded olanzapine (Zyprexa); adjunctive OLZ/SAM had no clinically significant effects on lithium or valproate pharmacokinetics. Additionally, OLZ/SAM had no clinically relevant effect on electrocardiogram parameters in a dedicated thorough QT study. Overall, safety and tolerability findings from clinical studies with OLZ/SAM indicate a similar safety profile to that of olanzapine, with the exception of less weight gain. As OLZ/SAM contains the opioid antagonist samidorphan, it is contraindicated in patients using opioids and in those undergoing acute opioid withdrawal. Clinical trial results from more than 1600 subjects support the use of OLZ/SAM as a new treatment option for patients with schizophrenia or BD-I.
format Online
Article
Text
id pubmed-8437420
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Dove
record_format MEDLINE/PubMed
spelling pubmed-84374202021-09-14 An Evidence-Based Review of OLZ/SAM for Treatment of Adults with Schizophrenia or Bipolar I Disorder Citrome, Leslie Graham, Christine Simmons, Adam Jiang, Ying Todtenkopf, Mark S Silverman, Bernard DiPetrillo, Lauren Cummings, Hannah Sun, Lei McDonnell, David Neuropsychiatr Dis Treat Review Olanzapine effectively treats schizophrenia and bipolar I disorder (BD-I); however, its use is limited by the risk of significant weight gain and metabolic effects. OLZ/SAM, a combination of olanzapine and samidorphan, was recently approved in the United States for the treatment of adults with schizophrenia or BD-I. OLZ/SAM provides the efficacy of olanzapine while mitigating olanzapine-associated weight gain through opioid-receptor blockade. Here, we summarize OLZ/SAM clinical data characterizing pharmacokinetics, antipsychotic efficacy, weight mitigation efficacy, safety, and long-term treatment effects. In an acute exacerbation of schizophrenia, OLZ/SAM and olanzapine provided similar symptom improvements versus placebo at week 4. In stable outpatients with schizophrenia, OLZ/SAM treatment resulted in significantly less weight gain, reducing the risk for clinically significant weight gain and waist circumference increases of ≥5 cm by half, compared with olanzapine at week 24. Based on open-label extension studies, OLZ/SAM is safe and well tolerated for up to 3.5 years of treatment, while maintaining schizophrenia symptom control and stabilizing weight. The olanzapine component of OLZ/SAM was bioequivalent to branded olanzapine (Zyprexa); adjunctive OLZ/SAM had no clinically significant effects on lithium or valproate pharmacokinetics. Additionally, OLZ/SAM had no clinically relevant effect on electrocardiogram parameters in a dedicated thorough QT study. Overall, safety and tolerability findings from clinical studies with OLZ/SAM indicate a similar safety profile to that of olanzapine, with the exception of less weight gain. As OLZ/SAM contains the opioid antagonist samidorphan, it is contraindicated in patients using opioids and in those undergoing acute opioid withdrawal. Clinical trial results from more than 1600 subjects support the use of OLZ/SAM as a new treatment option for patients with schizophrenia or BD-I. Dove 2021-09-09 /pmc/articles/PMC8437420/ /pubmed/34526769 http://dx.doi.org/10.2147/NDT.S313840 Text en © 2021 Citrome et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Review
Citrome, Leslie
Graham, Christine
Simmons, Adam
Jiang, Ying
Todtenkopf, Mark S
Silverman, Bernard
DiPetrillo, Lauren
Cummings, Hannah
Sun, Lei
McDonnell, David
An Evidence-Based Review of OLZ/SAM for Treatment of Adults with Schizophrenia or Bipolar I Disorder
title An Evidence-Based Review of OLZ/SAM for Treatment of Adults with Schizophrenia or Bipolar I Disorder
title_full An Evidence-Based Review of OLZ/SAM for Treatment of Adults with Schizophrenia or Bipolar I Disorder
title_fullStr An Evidence-Based Review of OLZ/SAM for Treatment of Adults with Schizophrenia or Bipolar I Disorder
title_full_unstemmed An Evidence-Based Review of OLZ/SAM for Treatment of Adults with Schizophrenia or Bipolar I Disorder
title_short An Evidence-Based Review of OLZ/SAM for Treatment of Adults with Schizophrenia or Bipolar I Disorder
title_sort evidence-based review of olz/sam for treatment of adults with schizophrenia or bipolar i disorder
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8437420/
https://www.ncbi.nlm.nih.gov/pubmed/34526769
http://dx.doi.org/10.2147/NDT.S313840
work_keys_str_mv AT citromeleslie anevidencebasedreviewofolzsamfortreatmentofadultswithschizophreniaorbipolaridisorder
AT grahamchristine anevidencebasedreviewofolzsamfortreatmentofadultswithschizophreniaorbipolaridisorder
AT simmonsadam anevidencebasedreviewofolzsamfortreatmentofadultswithschizophreniaorbipolaridisorder
AT jiangying anevidencebasedreviewofolzsamfortreatmentofadultswithschizophreniaorbipolaridisorder
AT todtenkopfmarks anevidencebasedreviewofolzsamfortreatmentofadultswithschizophreniaorbipolaridisorder
AT silvermanbernard anevidencebasedreviewofolzsamfortreatmentofadultswithschizophreniaorbipolaridisorder
AT dipetrillolauren anevidencebasedreviewofolzsamfortreatmentofadultswithschizophreniaorbipolaridisorder
AT cummingshannah anevidencebasedreviewofolzsamfortreatmentofadultswithschizophreniaorbipolaridisorder
AT sunlei anevidencebasedreviewofolzsamfortreatmentofadultswithschizophreniaorbipolaridisorder
AT mcdonnelldavid anevidencebasedreviewofolzsamfortreatmentofadultswithschizophreniaorbipolaridisorder
AT citromeleslie evidencebasedreviewofolzsamfortreatmentofadultswithschizophreniaorbipolaridisorder
AT grahamchristine evidencebasedreviewofolzsamfortreatmentofadultswithschizophreniaorbipolaridisorder
AT simmonsadam evidencebasedreviewofolzsamfortreatmentofadultswithschizophreniaorbipolaridisorder
AT jiangying evidencebasedreviewofolzsamfortreatmentofadultswithschizophreniaorbipolaridisorder
AT todtenkopfmarks evidencebasedreviewofolzsamfortreatmentofadultswithschizophreniaorbipolaridisorder
AT silvermanbernard evidencebasedreviewofolzsamfortreatmentofadultswithschizophreniaorbipolaridisorder
AT dipetrillolauren evidencebasedreviewofolzsamfortreatmentofadultswithschizophreniaorbipolaridisorder
AT cummingshannah evidencebasedreviewofolzsamfortreatmentofadultswithschizophreniaorbipolaridisorder
AT sunlei evidencebasedreviewofolzsamfortreatmentofadultswithschizophreniaorbipolaridisorder
AT mcdonnelldavid evidencebasedreviewofolzsamfortreatmentofadultswithschizophreniaorbipolaridisorder