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Not Yet Recruiting

A Study to Evaluate the Efficacy and Safety of KarXT for the Treatment of Manic Episodes in Bipolar-I Disorder (BALSAM-2) - CN012-0037

Mis à jour: 27 mai, 2025   |   ClinicalTrials.gov

Impression du resumé

SONGEZ-VOUS À PARTICIPER À CET ESSAI?
Imprimez cette page et le guide pour vous aider dans vos échanges avec votre médecin.
Utilisez le guide en matière d’essai pour connaître le processus de participation à un essai clinique. Soyez au fait des principaux facteurs à considérer avant de prendre une décision et dressez la liste des questions à poser à l’équipe de soins de santé.

Détails de l’essai

  • Phase 3

    Phase

  • Sexe(s)

  • 18-65

    Tranche d’âge

  • 30

    Emplacement(s)

  • Not Yet Recruiting

Options de traitement

Groupes de l’étude
INTERVENTION ATTRIBUÉE
Experimental: KarXT
Drug: KarXT
Placebo Comparator: Placebo
Other: Placebo

Principaux critères d’admissibilité

Inclusion Criteria: - Participants must have a primary diagnosis of Bipolar-I disorder established by a comprehensive psychiatric evaluation. - Participants must be experiencing an acute episode or relapse of mania or mania with mixed features (≤ 3 weeks). - Participants must require hospitalization for the acute exacerbation or relapse of mania. - Participants must have all psychotropic medications washed out in no more than 14 days prior to the first dose of the study drug. - Participants must have a Young Mania Rating Scale (YMRS) score of ≥ 20 at Screening and at Baseline. - Participants must have a Clinical Global Impressions-Bipolar (CGI-BP) ≥ 4 at Screening and at Baseline. Exclusion Criteria: - Participants must not have any primary Diagnostic and Statistical Manual of Mental Disorders (5th Edition, Text Revision) (DSM-5-TR) disorder, other than BP-I with mania or mania with mixed features within 12 months before screening, including BP-I with depression (for previous 3 months only), BP-II disorder, major depressive disorder, and primary psychotic disorder, with the exception of mild anxiety disorders. - Participants must not have a primary diagnosis of BP-I with rapid cycling (≥ 4 distinct mood episodes in one year). - Participants must not have a DSM-5-TR diagnosis of moderate to severe substance use disorder (except tobacco use disorder) within the 12 months before screening, or current use as determined by urine toxicology screen or alcohol test. - Participants must not be at risk for suicidal behavior at screening or the baseline visit as determined by the Investigator's clinical assessment and the Columbia-Suicide Severity Rating Scale (C-SSRS). - Participants must not have cirrhosis, liver cancer, clinically significant liver disease based on the liver function test results. - Other protocol-defined Inclusion/Exclusion criteria apply.

Nous vous recommandons fortement de contacter BMS pour signaler les effets secondaires (événements indésirables).
Les effets secondaires (événements indésirables) et les autres événements à signaler sont définis ici.
Signaler des effets secondaires (effets indésirables) ou des plaintes concernant la qualité du produit: Informations médicales

Des questions? Le support en direct est disponible 24/7 - Veuillez composer le 833-673-6134 ou Envoyez-nous un courriel

Des questions? Le support en direct est disponible 24/7 -
Veuillez composer le 833-673-6134 ou Envoyez-nous un courriel