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Investigational dopamine antagonists for the treatment of schizophrenia

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dc.contributor.authorWang, Sheng-Min-
dc.contributor.authorHan, Changsu-
dc.contributor.authorLee, Soo-Jung-
dc.contributor.authorJun, Tae-Youn-
dc.contributor.authorPatkar, Ashwin A.-
dc.contributor.authorMasand, Prakash S.-
dc.contributor.authorPae, Chi-Un-
dc.date.accessioned2021-09-03T14:58:42Z-
dc.date.available2021-09-03T14:58:42Z-
dc.date.created2021-06-16-
dc.date.issued2017-
dc.identifier.issn1354-3784-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/86303-
dc.description.abstractIntroduction: Schizophrenia is a debilitating illness with a chronic impact on social function and daily living. Although various antipsychotics are available, there are still many challenges and unmet needs. Thus, many compounds with diverse mechanisms have been investigated, but all approved antipsychotics still require interactions with dopamine D-2 receptors.Areas covered: We searched for investigational drugs using the key words dopamine' and schizophrenia' in American and European clinical trial registers (clinicaltrials.gov; clinicaltrialsregister.eu). Published articles were searched in PubMed, Embase, Medline, PsycINFO, Cumulative Index to Nursing and Allied Health Literature (CINAHL), the Web of Science and the Cochrane Central Register of Controlled Trials Library.Expert opinion: The prospect of developing a dopamine antagonist is hopeful. Brexpiprazole and cariprazine, which were agents listed as investigational dopamine antagonists,' just received FDA approval. Novel agents such as BL 1020, ITI-007, and JNJ-37822681 have solid published data available, and agents such as L-THP, Lu AF35700, S33138, and SB-773812 are under vigorous investigation. However, the expected benefits of the newly developed antagonists may not be great because they offer little enhanced efficacy for negative symptoms, cognition and functional outcomes.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherTAYLOR & FRANCIS LTD-
dc.subjectD-2 RECEPTOR ANTAGONIST-
dc.subjectATYPICAL ANTIPSYCHOTICS-
dc.subjectL-TETRAHYDROPALMATINE-
dc.subjectD3 RECEPTOR-
dc.subjectCOGNITIVE IMPAIRMENT-
dc.subjectCLINICAL DEVELOPMENT-
dc.subjectPREFRONTAL CORTEX-
dc.subjectDOUBLE-BLIND-
dc.subjectDRUGS-
dc.subjectHYPOTHESIS-
dc.titleInvestigational dopamine antagonists for the treatment of schizophrenia-
dc.typeArticle-
dc.contributor.affiliatedAuthorHan, Changsu-
dc.identifier.doi10.1080/13543784.2017.1323870-
dc.identifier.scopusid2-s2.0-85019961335-
dc.identifier.wosid000401712800004-
dc.identifier.bibliographicCitationEXPERT OPINION ON INVESTIGATIONAL DRUGS, v.26, no.6, pp.687 - 698-
dc.relation.isPartOfEXPERT OPINION ON INVESTIGATIONAL DRUGS-
dc.citation.titleEXPERT OPINION ON INVESTIGATIONAL DRUGS-
dc.citation.volume26-
dc.citation.number6-
dc.citation.startPage687-
dc.citation.endPage698-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusD-2 RECEPTOR ANTAGONIST-
dc.subject.keywordPlusATYPICAL ANTIPSYCHOTICS-
dc.subject.keywordPlusL-TETRAHYDROPALMATINE-
dc.subject.keywordPlusD3 RECEPTOR-
dc.subject.keywordPlusCOGNITIVE IMPAIRMENT-
dc.subject.keywordPlusCLINICAL DEVELOPMENT-
dc.subject.keywordPlusPREFRONTAL CORTEX-
dc.subject.keywordPlusDOUBLE-BLIND-
dc.subject.keywordPlusDRUGS-
dc.subject.keywordPlusHYPOTHESIS-
dc.subject.keywordAuthorSchizophrenia-
dc.subject.keywordAuthorInvestigational antipsychotics-
dc.subject.keywordAuthorPhase II-
dc.subject.keywordAuthoragonist-
dc.subject.keywordAuthorantagonist-
dc.subject.keywordAuthordopamine-
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