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Treatments in the pipeline for attention-deficit/hyperactivity disorder (ADHD) in adults.
Veronesi, Guilherme Fusetto; Gabellone, Alessandra; Tomlinson, Anneka; Solmi, Marco; Correll, Christoph U; Cortese, Samuele.
Affiliation
  • Veronesi GF; Southern Health NHS Foundation Trust, UK.
  • Gabellone A; DiBraiN-Department of Translational Biomedicine Neurosciences, University of Bari "Aldo Moro", Bari, Italy.
  • Tomlinson A; Department of Psychiatry, University of Oxford, Oxford, UK; Oxford Health NHS Foundation Trust, Oxford, UK.
  • Solmi M; Department of Psychiatry, University of Ottawa, Ottawa, ON, Canada; Department of Mental Health, The Ottawa Hospital, Ottawa, ON, Canada; Ottawa Hospital Research Institute (OHRI) Clinical Epidemiology Program, University of Ottawa, Ottawa, ON, Canada; School of Epidemiology and Public Health, Facul
  • Correll CU; Department of Child and Adolescent Psychiatry, Charité Universitätsmedizin, Berlin, Germany; The Zucker Hillside Hospital, Department of Psychiatry, Glen Oaks, NY, USA; Department of Psychiatry and Molecular Medicine, Donald and Barbara School of Medicine at Hofstra/Northwell, Hempstead, NY, USA; Ge
  • Cortese S; Centre for Innovation in Mental Health, School of Psychology, Faculty of Environmental and Life Sciences, University of Southampton, Southampton, UK; Clinical and Experimental Sciences (CNS and Psychiatry), Faculty of Medicine, University of Southampton, Southampton, UK; Solent NHS Trust, Southampto
Neurosci Biobehav Rev ; 163: 105774, 2024 Aug.
Article de En | MEDLINE | ID: mdl-38914177
ABSTRACT
To provide an overview of treatments in the pipeline for adults with attention-deficit/hyperactivity disorder (ADHD), we searched https//clinicaltrials.gov/and and https//www.clinicaltrialsregister.eu/ from 01/01/2010-10/18/2023 for ongoing or completed phase 2 or 3 randomised controlled trials (RCTs), assessing pharmacological or non-pharmacological interventions for adults with ADHD with no current regulatory approval. We found 90 eligible RCTs. Of these, 24 (27 %) reported results with statistical analysis for primary efficacy endpoints. While several pharmacological and non-pharmacological interventions had evidence of superiority compared to the control condition from a single RCT, centanafadine (norepinephrine, dopamine, and serotonin re-uptake inhibitor) was the only treatment with evidence of efficacy on ADHD core symptoms (small effect size=0.28-0.40) replicated in at least one additional RCT, alongside reasonable tolerability. Overall, the body of ongoing RCTs in adults with ADHD is insufficient, without any intervention on the horizon to match the efficacy of stimulant treatment or atomoxetine and with better tolerability profile. Additional effective and well tolerated treatments for adults with ADHD require development and testing.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Trouble déficitaire de l'attention avec hyperactivité Limites: Adult / Humans Langue: En Journal: Neurosci Biobehav Rev / Neurosci. biobehav. rev / Neuroscience and biobehavioral reviews Année: 2024 Type de document: Article Pays de publication: États-Unis d'Amérique

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Trouble déficitaire de l'attention avec hyperactivité Limites: Adult / Humans Langue: En Journal: Neurosci Biobehav Rev / Neurosci. biobehav. rev / Neuroscience and biobehavioral reviews Année: 2024 Type de document: Article Pays de publication: États-Unis d'Amérique