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dc.contributor.authorPisarska, Agnieszka
dc.contributor.authorDeluca, Paolo
dc.contributor.authorDemetrovics, Zsolt
dc.contributor.authorCorkery, John
dc.contributor.authorMoskalewicz, Jacek
dc.contributor.authorReDNet Group
dc.contributor.authorCorazza, Ornella
dc.contributor.authorCorkery, John
dc.contributor.authorStair, Jacqueline
dc.contributor.authorFergus, Suzanne
dc.contributor.authorPezzolesi, Cinzia
dc.contributor.authorSchifano, Fabrizio
dc.date.accessioned2020-03-22T01:20:42Z
dc.date.available2020-03-22T01:20:42Z
dc.date.issued2020-02-18
dc.identifier.citationPisarska , A , Deluca , P , Demetrovics , Z , Corkery , J , Moskalewicz , J , ReDNet Group , , Corazza , O , Corkery , J , Stair , J , Fergus , S , Pezzolesi , C & Schifano , F 2020 , ' Novel psychoactive substances (NPS) – knowledge and experiences of drug users from Hungary, Poland, the UK and the USA ' , Neuropsychopharmacologia Hungarica , vol. 21 , no. 3 , pp. 152-163 .
dc.identifier.issn1419-8711
dc.identifier.otherORCID: /0000-0002-7134-0665/work/70885847
dc.identifier.otherORCID: /0000-0001-7371-319X/work/98163899
dc.identifier.urihttp://hdl.handle.net/2299/22450
dc.descriptionFunding Information: This publication arises from the activities of the RedNet Research Project which have received funding from the EU in the framework of the Public Health Programme (2009 12 16). Zsolt Demetrovics acknowledges the support of the Hungarian National Research, Development and Innovation Office (Grant numbers: K111938, KKP126835). Funding Information: Acknowledgment: This publication arises from the activities of the RedNet Research Project which have received funding from the EU in the framework of the Public Health Programme (2009 12 16). Zsolt Demetrovics acknowledges the support of the Hungarian National Research, Development and Innovation Office (Grant numbers: K111938, KKP126835). Publisher Copyright: © 2019, Hungarian Association of Psychopharmacology. All rights reserved.
dc.description.abstractDopamine D 3 receptor partial agonists represent a new generation of atypical antipsychotics. Cariprazine, which has received centralized market authorization from the European Medicines Agency in 2017 for the treatment of adult patients with schizophrenia (including those with predominant negative symptoms of schizophrenia) differs from the other two partial agonist antipsychotics aripiprazole and brexpiprazole due to its unique features. Cariprazine is a dopamine D 3 preferring D 3/D2 partial agonist with very similar dopamine receptor sub-type selectivity as dopamine. It has proven efficacy in the treatment of positive and negative symptoms of schizophrenia, as well as for relapse prevention. Further phase-3 clinical studies proved the efficacy of cariprazine in the acute treatment of manic or mixed episodes associated with bipolar I disorder, as well as in bipolar depression. For the adjunctive treatment of major depressive disorder, phase 3 studies are in progress.en
dc.format.extent11
dc.format.extent146428
dc.language.isoeng
dc.relation.ispartofNeuropsychopharmacologia Hungarica
dc.subjectnovel psychoactive substances
dc.subjectdrugs
dc.subjectaddiction
dc.subjectdelegalisation
dc.subjectinternational study
dc.subjectPredominant negative symptoms
dc.subjectAtypical antipsychotic
dc.subjectCariprazine
dc.subjectSchizophrenia
dc.subjectDopamine D and D receptor partial agonist
dc.subjectClinical Neurology
dc.subjectNeuropsychology and Physiological Psychology
dc.subjectNeuroscience(all)
dc.subjectPharmacology, Toxicology and Pharmaceutics(all)
dc.titleNovel psychoactive substances (NPS) – knowledge and experiences of drug users from Hungary, Poland, the UK and the USAen
dc.contributor.institutionCentre for Clinical Practice, Safe Medicines and Drug Misuse Research
dc.contributor.institutionCentre for Health Services and Clinical Research
dc.contributor.institutionPsychopharmacology, Drug Misuse and Novel Psychoactive Substances Unit
dc.contributor.institutionSchool of Life and Medical Sciences
dc.contributor.institutionDepartment of Clinical, Pharmaceutical and Biological Science
dc.contributor.institutionCentre for Future Societies Research
dc.contributor.institutionCentre for Hazard Detection and Protection Research
dc.contributor.institutionCentre for Research in Mechanisms of Disease and Drug Discovery
dc.contributor.institutionNanopharmaceutics
dc.contributor.institutionNatural Product Chemistry and Drug Design
dc.description.statusPeer reviewed
dc.identifier.urlhttps://pubmed.ncbi.nlm.nih.gov/32015192/
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue


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