Asenapine


Asenapine, sold under the brand name Saphris among others, is an atypical antipsychotic medication used to treat schizophrenia and acute mania associated with bipolar disorder as well as the medium to long-term management of bipolar disorder.
It was chemically derived via altering the chemical structure of the tetracyclic antidepressant, mianserin.
It was initially approved in the United States in 2009 and approved as a generic medication in 2020.

Medical uses

Asenapine has been approved by the FDA for the acute treatment of adults with schizophrenia and acute treatment of manic or mixed episodes associated with bipolar I disorder with or without psychotic features in adults. In Australia asenapine's approved indications include the following:
  • Schizophrenia
  • Treatment, for up to 6 months, of an episode of acute mania or mixed episodes associated with bipolar I disorder
  • Maintenance treatment, as monotherapy, of bipolar I disorder
In the European Union and the United Kingdom, asenapine is only licensed for use as a treatment for acute mania in bipolar I disorder.
Asenapine is absorbed readily if administered sublingually, but is poorly absorbed when swallowed. A transdermal formulation of asenapine was approved in the United States in October 2019 under the brand name Secuado.

Schizophrenia

A Cochrane systematic review found that while Asenapine has some preliminary evidence that it improves positive, negative, and depressive symptoms, it does not have enough research to merit a certain recommendation of asenapine for the treatment of schizophrenia.

Bipolar disorder

For the medium-term and long-term management and control of both depressive and manic features of bipolar disorder asenapine was found to be equally effective as olanzapine, but with a substantially superior side effect profile.
In acute mania, asenapine was found to be significantly superior to placebo. As for its efficacy in the treatment of acute mania, a recent meta-analysis showed that it produces comparatively small improvements in manic symptoms in patients with acute mania and mixed episodes than most other antipsychotic drugs such as risperidone and olanzapine. Drop-out rates were also unusually high with asenapine. According to a post-hoc analysis of two 3-week clinical trials it may possess some antidepressant effects in patients with acute mania or mixed episodes.

Adverse effects

Adverse effect incidence
Very common adverse effects include:
Common adverse effects include:
Uncommon adverse effects include:
Rare adverse effects include:
Unknown incidence adverse effects
Asenapine seems to have a relatively low weight gain liability for an atypical antipsychotic and a 2013 meta-analysis found significantly less weight gain than, paliperidone, risperidone, quetiapine, sertindole, chlorpromazine, iloperidone, clozapine, zotepine and olanzapine and approximately as much as weight gain as aripiprazole, lurasidone, amisulpride, haloperidol and ziprasidone. Its potential for elevating plasma prolactin levels seems relatively limited too according to this meta-analysis. This meta-analysis also found that asenapine has approximately the same odds ratio for causing sedation as olanzapine and haloperidol and a higher odds ratio for sedation than aripiprazole, paliperidone and amisulpride to name a few and is hence a mild-moderately sedating antipsychotic. The same meta-analysis suggested that asenapine had a relatively high risk of extrapyramidal symptoms compared to other atypical antipsychotics but a lower risk than first-generation or typical antipsychotics.

Discontinuation

For all antipsychotics, the British National Formulary recommends a gradual dose reduction when discontinuing to avoid acute withdrawal syndrome or rapid relapse. Symptoms of withdrawal commonly include nausea, vomiting, and loss of appetite. Other symptoms may include restlessness, increased sweating, and trouble sleeping. Less commonly there may be a feeling of the world spinning, numbness, or muscle pains. Symptoms generally resolve after a short period of time.
There is tentative evidence that discontinuation of antipsychotics can result in psychosis as a transient withdrawal symptom. It may also result in recurrence of the condition that is being treated. Rarely tardive dyskinesia can occur when the medication is stopped.

Pharmacology

Pharmacodynamics

SitepKiKi Action
5-HT1A8.62.5Partial agonist
5-HT1B8.44.0Antagonist
5-HT2A10.20.06Antagonist
5-HT2B9.80.16Antagonist
5-HT2C10.50.03Antagonist
5-HT5A8.81.6Antagonist
5-HT69.50.25Antagonist
5-HT79.90.13Antagonist
α18.91.2Antagonist
α2A8.91.2Antagonist
α2B9.50.32Antagonist
α2C8.91.2Antagonist
D18.91.4Antagonist
D28.91.3Antagonist
D39.40.42Antagonist
D49.01.1Antagonist
H19.01.0Antagonist
H28.26.2Antagonist
mACh<58128Antagonist

Asenapine shows high affinity for numerous receptors, including the serotonin 5-HT1A, 5-HT1B, 5-HT2A, 5-HT2B, 5-HT2C, 5-HT5A, 5-HT6, and 5-HT7 receptors, the adrenergic α1, α2A, α2B, and α2C receptors, the dopamine D1, D2, D3, and D4 receptors, and the histamine H1 and H2 receptors. It has much lower affinity for the muscarinic acetylcholine receptors. Asenapine behaves as a partial agonist at the 5-HT1A receptors. At all other targets asenapine is an antagonist.
Even relative to other atypical antipsychotics, asenapine has unusually high affinity for the 5-HT2A, 5-HT2C, 5-HT6, and 5-HT7 receptors, and very high affinity for the α2 and H1 receptors.