Evidence map›Paper›PMID 20642375›Full record

ReviewExpert opinion on pharmacotherapy2010

Evaluation of the clinical efficacy of asenapine in schizophrenia.

Arpi Minassian, Jared W Young

Open access · greenAbstract readReview
In one paragraph

Review in Expert opinion on pharmacotherapy, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.6field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 27 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Article
  5. Transdermal Asenapine in Schizophrenia: A Systematic Review.Patient preference and adherence · 2020
    Review
  6. Review
  7. Article
  8. Newer antipsychotics and upcoming molecules for schizophrenia.European journal of clinical pharmacology · 2013
    Review
  9. Review
  10. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Arpi MinassianUniversity of California San Diego, Department of Psychiatry, La Jolla, California 92093-0804, USA.
Jared W Young
University of California, San Diego · US

Funding

Inhibitory Deficits in Mania and Hyperdopaminiergic MiceR01MH071916 · NIMH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GEYER, MARK A, PERRY, WILLIAM · 2004 to 2014
$4.2M
The rodent continuous performance task: Filling the vigilance translational gapR21MH085221 · NIMH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI YOUNG, JARED WILLIAM · 2009 to 2010
$418k
NIMH NIH HHS R01 MH071916NIMH NIH HHS R21 MH085221
6 · The paper itself

Abstract

importance of the fieldAsenapine is a new atypical antipsychotic medication with high affinity for D(2) and 5HT(2A) receptors that has been approved by the FDA in adults for the acute treatment of schizophrenia in the USA. The purpose of this review is to describe the compound and examine whether it addresses some of the unmet clinical needs in treating schizophrenia. AREAS COVERED IN THIS REVIEW: The development of asenapine is described with attention to its chemistry, pharmacodynamic and pharmacokinetic profile. Preclinical and clinical trials of safety and efficacy are reviewed. The advantages and disadvantages of asenapine relative to other antipsychotic medications are discussed. WHAT THE READER WILL GAIN: Asenapine will be evaluated for whether it: i) causes a reduction in symptoms of schizophrenia; ii) has a side-effect profile minimizing extrapyramidal symptoms, weight gain and cardiac effects; and iii) affects negative and/or cognitive symptoms. TAKE HOME MESSAGE: Asenapine is a recently approved agent with an acceptable cardiometabolic profile and exhibits similar efficacy as other antipsychotic medications, primarily on positive symptoms of schizophrenia. Relatively less weight gain compared with other agents may confer a notable advantage. Sublingual administration may have positive and negative effects on patient compliance. Potential 'pro-cognitive' effects of asenapine are preliminary and require more investigation.

Indexed as

Antipsychotic AgentsDibenzocycloheptenesDopamine AntagonistsHeterocyclic Compounds, 4 or More RingsHumansSchizophreniaSerotonin AntagonistsTreatment OutcomeAntipsychotic AgentsasenapineDibenzocycloheptenesDopamine AntagonistsHeterocyclic Compounds, 4 or More RingsSerotonin Antagonists

Identifiers

PMID20642375
PMCPMC2924192
OpenAlexW2114618400

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.