Asenapine: an atypical antipsychotic with atypical formulations

Asenapine is a second-generation (atypical) antipsychotic medication not available in a pill that can be swallowed; rather, it is commercialized in sublingual and transdermal formulations. This is a consequence of extensive first-pass metabolism if ingested. The sublingual formulation is approved in...

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Main Authors: Meghan Musselman, Justin Faden, Leslie Citrome
Format: Article
Language:English
Published: SAGE Publishing 2021-09-01
Series:Therapeutic Advances in Psychopharmacology
Online Access:https://doi.org/10.1177/20451253211035269
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spelling doaj-a1a324bb8e624cab930d56ad2ff0a4b72021-09-11T21:33:30ZengSAGE PublishingTherapeutic Advances in Psychopharmacology2045-12612021-09-011110.1177/20451253211035269Asenapine: an atypical antipsychotic with atypical formulationsMeghan MusselmanJustin FadenLeslie CitromeAsenapine is a second-generation (atypical) antipsychotic medication not available in a pill that can be swallowed; rather, it is commercialized in sublingual and transdermal formulations. This is a consequence of extensive first-pass metabolism if ingested. The sublingual formulation is approved in many jurisdictions for the treatment of schizophrenia and manic or mixed episodes associated with bipolar I disorder and is available generically. The efficacy profile is well characterized in a number of clinical trials, including an off-label use for the management of agitation. Obstacles to its use include food and drink restrictions, twice-daily dosing and adverse effects such as dysgeusia (distorted, altered, or unpleasant taste) and oral hypoesthesia (numbness). Transdermal asenapine was approved by the US Food and Drug Administration in 2019 for the treatment of schizophrenia in adults. Efficacy was established in a registrational study examining acutely ill inpatients with schizophrenia. The patch needs to changed once daily. Obstacles to its use include the potential for skin reactions such as erythema and pruritis, and being a branded product, it is more costly than other options. This is a narrative review of the chemistry and pharmacokinetics/pharmacodynamics of asenapine, as well as summarizing the efficacy and tolerability of both sublingual and transdermal asenapine, and its possible place in treatment.https://doi.org/10.1177/20451253211035269
collection DOAJ
language English
format Article
sources DOAJ
author Meghan Musselman
Justin Faden
Leslie Citrome
spellingShingle Meghan Musselman
Justin Faden
Leslie Citrome
Asenapine: an atypical antipsychotic with atypical formulations
Therapeutic Advances in Psychopharmacology
author_facet Meghan Musselman
Justin Faden
Leslie Citrome
author_sort Meghan Musselman
title Asenapine: an atypical antipsychotic with atypical formulations
title_short Asenapine: an atypical antipsychotic with atypical formulations
title_full Asenapine: an atypical antipsychotic with atypical formulations
title_fullStr Asenapine: an atypical antipsychotic with atypical formulations
title_full_unstemmed Asenapine: an atypical antipsychotic with atypical formulations
title_sort asenapine: an atypical antipsychotic with atypical formulations
publisher SAGE Publishing
series Therapeutic Advances in Psychopharmacology
issn 2045-1261
publishDate 2021-09-01
description Asenapine is a second-generation (atypical) antipsychotic medication not available in a pill that can be swallowed; rather, it is commercialized in sublingual and transdermal formulations. This is a consequence of extensive first-pass metabolism if ingested. The sublingual formulation is approved in many jurisdictions for the treatment of schizophrenia and manic or mixed episodes associated with bipolar I disorder and is available generically. The efficacy profile is well characterized in a number of clinical trials, including an off-label use for the management of agitation. Obstacles to its use include food and drink restrictions, twice-daily dosing and adverse effects such as dysgeusia (distorted, altered, or unpleasant taste) and oral hypoesthesia (numbness). Transdermal asenapine was approved by the US Food and Drug Administration in 2019 for the treatment of schizophrenia in adults. Efficacy was established in a registrational study examining acutely ill inpatients with schizophrenia. The patch needs to changed once daily. Obstacles to its use include the potential for skin reactions such as erythema and pruritis, and being a branded product, it is more costly than other options. This is a narrative review of the chemistry and pharmacokinetics/pharmacodynamics of asenapine, as well as summarizing the efficacy and tolerability of both sublingual and transdermal asenapine, and its possible place in treatment.
url https://doi.org/10.1177/20451253211035269
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