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Newer antipsychotics and upcoming molecules for schizophrenia

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Abstract

Background

The management of schizophrenia has seen significant strides over the last few decades, due to the increasing availability of a number of antipsychotics. Yet, the diminished efficacy in relation to the negative and cognitive symptoms of schizophrenia, and the disturbing adverse reactions associated with the current antipsychotics, reflect the need for better molecules targeting unexplored pathways.

Purpose

To review the salient features of the recently approved antipsychotics; namely, iloperidone, asenapine, lurasidone and blonanserin.

Methods

We discuss the advantages, limitations and place in modern pharmacotherapy of each of these drugs. In addition, we briefly highlight the new targets that are being explored.

Results

Promising strategies include modulation of the glutamatergic and GABAergic pathways, as well as cholinergic systems.

Conclusions

Although regulatory bodies have approved only a handful of antipsychotics in recent years, the wide spectrum of targets that are being explored could eventually bring out antipsychotics with improved efficacy and acceptability, as well as the potential to revolutionize psychiatric practice.

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Abbreviations

BPRS:

Brief Psychiatric Rating Scale

CANTAB:

Cambridge Neuropsychological Test Automated Battery

CGI-S:

Clinical Global Impression Severity scale

DLPFC:

Dorsolateral prefrontal cortex

EPS:

Extrapyramidal symptoms

MATRICS:

Measurement and Treatment Research to Improve Cognition in Schizophrenia

MCCB:

Matrics Consensus Cognitive Battery

nAchR:

Neuronal nicotinic acetylcholine receptors

PANSS-T:

Positive and negative syndrome scale total score

PDE:

Phosphodiesterase

QoLS:

Quality of Life Scale

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George, M., Amrutheshwar, R., Rajkumar, R.P. et al. Newer antipsychotics and upcoming molecules for schizophrenia. Eur J Clin Pharmacol 69, 1497–1509 (2013). https://doi.org/10.1007/s00228-013-1498-4

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  • DOI: https://doi.org/10.1007/s00228-013-1498-4

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