Cargando…

NBI‐98854, a selective monoamine transport inhibitor for the treatment of tardive dyskinesia: A randomized, double‐blind, placebo‐controlled study

BACKGROUND: Tardive dyskinesia is a persistent movement disorder induced by chronic neuroleptic exposure. NBI‐98854 is a novel, highly selective, vesicular monoamine transporter 2 inhibitor. We present results of a randomized, 6‐week, double‐blind, placebo‐controlled, dose‐titration study evaluating...

Descripción completa

Detalles Bibliográficos
Autores principales: O'Brien, Christopher F., Jimenez, Roland, Hauser, Robert A., Factor, Stewart A., Burke, Joshua, Mandri, Daniel, Castro‐Gayol, Julio C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5049616/
https://www.ncbi.nlm.nih.gov/pubmed/26346941
http://dx.doi.org/10.1002/mds.26330
_version_ 1782457752289804288
author O'Brien, Christopher F.
Jimenez, Roland
Hauser, Robert A.
Factor, Stewart A.
Burke, Joshua
Mandri, Daniel
Castro‐Gayol, Julio C.
author_facet O'Brien, Christopher F.
Jimenez, Roland
Hauser, Robert A.
Factor, Stewart A.
Burke, Joshua
Mandri, Daniel
Castro‐Gayol, Julio C.
author_sort O'Brien, Christopher F.
collection PubMed
description BACKGROUND: Tardive dyskinesia is a persistent movement disorder induced by chronic neuroleptic exposure. NBI‐98854 is a novel, highly selective, vesicular monoamine transporter 2 inhibitor. We present results of a randomized, 6‐week, double‐blind, placebo‐controlled, dose‐titration study evaluating the safety, tolerability, and efficacy of NBI‐98854 for the treatment of tardive dyskinesia. METHODS: Male and female adult subjects with moderate or severe tardive dyskinesia were included. NBI‐98854 or placebo was given once per day starting at 25 mg and then escalated by 25 mg to a maximum of 75 mg based on dyskinesia and tolerability assessment. The primary efficacy endpoint was the change in Abnormal Involuntary Movement Scale from baseline at week 6 scored by blinded, central video raters. The secondary endpoint was the Clinical Global Impression of Change—Tardive Dyskinesia score assessed by the blinded investigator. RESULTS: Two hundred five potential subjects were screened, and 102 were randomized; 76% of NBI‐98854 subjects and 80% of placebo subjects reached the maximum allowed dose. Abnormal Involuntary Movement Scale scores for NBI‐98854 compared with placebo were significantly reduced (p = 0.0005). Active drug was also superior on the Clinical Global Impression of Change—Tardive Dyskinesia (p < 0.0001). Treatment‐emergent adverse event rates were 49% in the NBI‐98854 and 33% in the placebo subjects. The most common adverse events (active vs. placebo) were fatigue and headache (9.8% vs. 4.1%) and constipation and urinary tract infection (3.9% vs. 6.1%). No clinically relevant changes in safety assessments were noted. CONCLUSION: NBI‐98854 significantly improved tardive dyskinesia and was well tolerated in patients. These results support the phase 3 clinical trials of NBI‐98854 now underway. © 2015 The Authors. Movement Disorders published by Wiley Periodicals, Inc. on behalf of International Parkinson and Movement Disorder Society.
format Online
Article
Text
id pubmed-5049616
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-50496162016-10-06 NBI‐98854, a selective monoamine transport inhibitor for the treatment of tardive dyskinesia: A randomized, double‐blind, placebo‐controlled study O'Brien, Christopher F. Jimenez, Roland Hauser, Robert A. Factor, Stewart A. Burke, Joshua Mandri, Daniel Castro‐Gayol, Julio C. Mov Disord Research Articles BACKGROUND: Tardive dyskinesia is a persistent movement disorder induced by chronic neuroleptic exposure. NBI‐98854 is a novel, highly selective, vesicular monoamine transporter 2 inhibitor. We present results of a randomized, 6‐week, double‐blind, placebo‐controlled, dose‐titration study evaluating the safety, tolerability, and efficacy of NBI‐98854 for the treatment of tardive dyskinesia. METHODS: Male and female adult subjects with moderate or severe tardive dyskinesia were included. NBI‐98854 or placebo was given once per day starting at 25 mg and then escalated by 25 mg to a maximum of 75 mg based on dyskinesia and tolerability assessment. The primary efficacy endpoint was the change in Abnormal Involuntary Movement Scale from baseline at week 6 scored by blinded, central video raters. The secondary endpoint was the Clinical Global Impression of Change—Tardive Dyskinesia score assessed by the blinded investigator. RESULTS: Two hundred five potential subjects were screened, and 102 were randomized; 76% of NBI‐98854 subjects and 80% of placebo subjects reached the maximum allowed dose. Abnormal Involuntary Movement Scale scores for NBI‐98854 compared with placebo were significantly reduced (p = 0.0005). Active drug was also superior on the Clinical Global Impression of Change—Tardive Dyskinesia (p < 0.0001). Treatment‐emergent adverse event rates were 49% in the NBI‐98854 and 33% in the placebo subjects. The most common adverse events (active vs. placebo) were fatigue and headache (9.8% vs. 4.1%) and constipation and urinary tract infection (3.9% vs. 6.1%). No clinically relevant changes in safety assessments were noted. CONCLUSION: NBI‐98854 significantly improved tardive dyskinesia and was well tolerated in patients. These results support the phase 3 clinical trials of NBI‐98854 now underway. © 2015 The Authors. Movement Disorders published by Wiley Periodicals, Inc. on behalf of International Parkinson and Movement Disorder Society. John Wiley and Sons Inc. 2015-09-08 2015-10 /pmc/articles/PMC5049616/ /pubmed/26346941 http://dx.doi.org/10.1002/mds.26330 Text en © 2015 The Authors. Movement Disorders published by Wiley Periodicals, Inc. on behalf of International Parkinson and Movement Disorder Society This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
O'Brien, Christopher F.
Jimenez, Roland
Hauser, Robert A.
Factor, Stewart A.
Burke, Joshua
Mandri, Daniel
Castro‐Gayol, Julio C.
NBI‐98854, a selective monoamine transport inhibitor for the treatment of tardive dyskinesia: A randomized, double‐blind, placebo‐controlled study
title NBI‐98854, a selective monoamine transport inhibitor for the treatment of tardive dyskinesia: A randomized, double‐blind, placebo‐controlled study
title_full NBI‐98854, a selective monoamine transport inhibitor for the treatment of tardive dyskinesia: A randomized, double‐blind, placebo‐controlled study
title_fullStr NBI‐98854, a selective monoamine transport inhibitor for the treatment of tardive dyskinesia: A randomized, double‐blind, placebo‐controlled study
title_full_unstemmed NBI‐98854, a selective monoamine transport inhibitor for the treatment of tardive dyskinesia: A randomized, double‐blind, placebo‐controlled study
title_short NBI‐98854, a selective monoamine transport inhibitor for the treatment of tardive dyskinesia: A randomized, double‐blind, placebo‐controlled study
title_sort nbi‐98854, a selective monoamine transport inhibitor for the treatment of tardive dyskinesia: a randomized, double‐blind, placebo‐controlled study
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5049616/
https://www.ncbi.nlm.nih.gov/pubmed/26346941
http://dx.doi.org/10.1002/mds.26330
work_keys_str_mv AT obrienchristopherf nbi98854aselectivemonoaminetransportinhibitorforthetreatmentoftardivedyskinesiaarandomizeddoubleblindplacebocontrolledstudy
AT jimenezroland nbi98854aselectivemonoaminetransportinhibitorforthetreatmentoftardivedyskinesiaarandomizeddoubleblindplacebocontrolledstudy
AT hauserroberta nbi98854aselectivemonoaminetransportinhibitorforthetreatmentoftardivedyskinesiaarandomizeddoubleblindplacebocontrolledstudy
AT factorstewarta nbi98854aselectivemonoaminetransportinhibitorforthetreatmentoftardivedyskinesiaarandomizeddoubleblindplacebocontrolledstudy
AT burkejoshua nbi98854aselectivemonoaminetransportinhibitorforthetreatmentoftardivedyskinesiaarandomizeddoubleblindplacebocontrolledstudy
AT mandridaniel nbi98854aselectivemonoaminetransportinhibitorforthetreatmentoftardivedyskinesiaarandomizeddoubleblindplacebocontrolledstudy
AT castrogayoljulioc nbi98854aselectivemonoaminetransportinhibitorforthetreatmentoftardivedyskinesiaarandomizeddoubleblindplacebocontrolledstudy