Brexpiprazole: so far so good. (February 2016)
- Record Type:
- Journal Article
- Title:
- Brexpiprazole: so far so good. (February 2016)
- Main Title:
- Brexpiprazole: so far so good
- Authors:
- Das, Saibal
Barnwal, Preeti
Winston A, Blessed
Mondal, Somnath
Saha, Indranil - Abstract:
- This article describes the role of a newly approved antipsychotic agent brexpiprazole in the treatment of schizophrenia and major depressive disorder. This drug has high affinity for 5-HT1A, 5-HT2A, D2 and α1B, 2C receptors. It displays partial agonism at 5-HT1A and D2 receptors and potent antagonism at 5-HT2A and α1B, 2C adrenergic receptors. It also has some affinity (antagonism) for D3, 5-HT2B, 5-HT7 and α1A, 1D receptors, and moderate affinity for H1 and low affinity for M1 receptors. These all lead to a favorable antipsychotic profile in terms of improvement of cognitive performance and sleep patterns, as well as effects on affective states and potential to treat core symptoms in schizophrenia and major depressive disorder, including cognitive deficits with a low risk of adverse effects (extrapyramidal symptoms, metabolic complications, weight gain, akathisia potential) that are commonly encountered with other typical and second-generation antipsychotic drugs. In our review, we have made an attempt to decipher the pharmacological profile of brexpiprazole from two major trials (VECTOR and BEACON). We have also tried to give a concise but detailed overview of brexpiprazole by head to head comparison of the pharmacological profile of brexpiprazole and its earlier congeners aripiprazole and prototype antipsychotic drug chlorpromazine by accessing individual summaries of product characteristics from the US Food and Drug Administration database, 2015. Relevant preclinical andThis article describes the role of a newly approved antipsychotic agent brexpiprazole in the treatment of schizophrenia and major depressive disorder. This drug has high affinity for 5-HT1A, 5-HT2A, D2 and α1B, 2C receptors. It displays partial agonism at 5-HT1A and D2 receptors and potent antagonism at 5-HT2A and α1B, 2C adrenergic receptors. It also has some affinity (antagonism) for D3, 5-HT2B, 5-HT7 and α1A, 1D receptors, and moderate affinity for H1 and low affinity for M1 receptors. These all lead to a favorable antipsychotic profile in terms of improvement of cognitive performance and sleep patterns, as well as effects on affective states and potential to treat core symptoms in schizophrenia and major depressive disorder, including cognitive deficits with a low risk of adverse effects (extrapyramidal symptoms, metabolic complications, weight gain, akathisia potential) that are commonly encountered with other typical and second-generation antipsychotic drugs. In our review, we have made an attempt to decipher the pharmacological profile of brexpiprazole from two major trials (VECTOR and BEACON). We have also tried to give a concise but detailed overview of brexpiprazole by head to head comparison of the pharmacological profile of brexpiprazole and its earlier congeners aripiprazole and prototype antipsychotic drug chlorpromazine by accessing individual summaries of product characteristics from the US Food and Drug Administration database, 2015. Relevant preclinical and clinical studies associated with this drug have been discussed with emphasis on efficacy and safety concerns. From the studies done so far, it can be concluded that brexpiprazole can be an effective monotherapy for schizophrenia and as an adjunct to other antidepressant medications in major depressive disorder. … (more)
- Is Part Of:
- Therapeutic advances in psychopharmacology. Volume 6:Number 1(2016:Feb.)
- Journal:
- Therapeutic advances in psychopharmacology
- Issue:
- Volume 6:Number 1(2016:Feb.)
- Issue Display:
- Volume 6, Issue 1 (2016)
- Year:
- 2016
- Volume:
- 6
- Issue:
- 1
- Issue Sort Value:
- 2016-0006-0001-0000
- Page Start:
- 39
- Page End:
- 54
- Publication Date:
- 2016-02
- Subjects:
- antipsychotic -- brexpiprazole -- major depressive disorder -- schizophrenia
Psychopharmacology -- Periodicals
Psychotherapy -- Periodicals
615.7805 - Journal URLs:
- http://tpp.sagepub.com/ ↗
http://www.uk.sagepub.com/home.nav ↗
http://www.uk.sagepub.com/journals/Journal201949 ↗ - DOI:
- 10.1177/2045125315614739 ↗
- Languages:
- English
- ISSNs:
- 2045-1253
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 6586.xml