A Study to Evaluate the Efficacy and Safety of KarXT for the Treatment of Manic Episodes in Bipolar-I Disorder
Ориентир для пациента и семьи
Простыми словами
Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.
- Что изучают
- В протоколе указаны: KarXT, Placebo.
- Кому может быть актуально
- Состояния в реестре: Bipolar-I Disorder With Mania or Mania With Mixed Features. Базовые параметры: 18 лет — 65 лет · Все.
- Что важно проверить
- Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
- Где проводится
- США, Аргентина, Австралия, Болгария, Венгрия +4
- Следующий шаг
- Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Не всё понятно в терминах? Прочитайте наш гид для пациентов →
Официальное название
A Phase 3, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of KarXT for the Treatment of Manic Episodes in Bipolar-I Disorder (BALSAM-1)
Обзор
The purpose of this study is to evaluate the efficacy and safety of KarXT for the treatment of manic episodes in Bipolar-I Disorder
Подробное описание
This is a Phase 3, randomized, double-blind, placebo-controlled, multicenter, inpatient study in subjects with bipolar disorder experiencing an acute episode of mania or mania with mixed features.
The primary objective of the study is to evaluate the efficacy of KarXT compared to placebo in treating symptoms of mania during a 3-week inpatient period. The duration of the study including screening, the double-blind inpatient treatment period and safety-follow-up is no more than seven weeks.
Вмешательства
- Препарат KarXT
Specified dose on specified days - Другое Placebo
Specified dose on specified days
Первичные конечные точки
- Change from baseline in Young Mania Rating Scale (YMRS) score [Срок оценки: At week 3]
Вторичные конечные точки (3)
- Change from baseline in Clinical Global Impressions-Bipolar (CGI-BP) [Срок оценки: At week 3]
- Occurrence of response based on a ≥ 50% decrease from baseline in YMRS total score [Срок оценки: At week 3]
- Occurrence of response based on CGI-BP change from baseline ≥ 1 [Срок оценки: At week 3]
Критерии участия
Критерии включения
- 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.
Критерии исключения
- 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, borderline personality 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 a history of irritable bowel syndrome (with or without constipation) or serious constipation requiring treatment within the last 6 months.
- Participants must not have a history or high risk of urinary retention, gastric retention, or untreated narrow-angle glaucoma.
- Other protocol-defined Inclusion/Exclusion criteria apply.
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Нет
Дизайн исследования
- Распределение
- Рандомизированное
- Модель
- Параллельные группы
- Маскирование
- Двойное слепое
- Основная цель
- Лечение
Центры проведения
США · 22 центра
- Local Institution - 0058 — Bentonville
- Woodland International Research Group — Little Rock
- Advanced Research Center Inc. — Anaheim
- CITrials — Bellflower
- Local Institution - 0014 — Cerritos
- Collaborative Neuroscience Research, LLC — Long Beach
- NRC Research Institute — Los Angeles
- Catalina Research Institute, LLC — Montclair
- … и ещё 14 центров
Япония · 19 центров
- Hotei Hospital — Kōnan
- Okehazama Hospital — Toyoake
- National Kohnodai Medical Center. — Ichikawa
- Local Institution - 0100 — Kitakyushu
- Obihiro Kosei Hospital — Obihiro
- Goryokai Medical Corporation - Goryokai Hospital — Sapporo
- Kansai Medical University Medical Center — Moriguchi
- Rainbow and Sea Hospital — Karatsu-shi
- … и ещё 11 центров
Болгария · 7 центров
- Local Institution - 0138 — Kazanlak
- Center for Mental Health Prof. Dr. Ivan Temkov — Burgas
- Local Institution - 0139 — Haskovo
- State Psychiatric Hospital Sv. Ivan Rilski Novi Iskar — Novi Iskar
- "University Multiprofile Hospital for Active Treatment - Dr. Georgi Stranski" EAD — Pleven
- MHAT "Dr. Ival Seliminski" — Sliven
- Mental Health Center - Vratsa — Vratsa
Польша · 7 центров
- Centrum Medyczne HCP — Poznan
- Instytut Psychiatrii i Neurologii — Warsaw
- Klinika Psychiatrii Uniwersytet Medyczny w Białymstoku — Bialystok
- Local Institution - 0111 — Gdansk
- M2M Med — Rybnik
- Local Institution - 0102 — Sosnowiec
- Clinica Inventiva — Tuszyn
Украина · 7 центров
- Local Institution - 0131 — Smila
- Local Institution - 0133 — Skarzhyntsi
- Local Institution - 0130 — Dnipro
- Local Institution - 0126 — Kropyvnytskyi
- Local Institution - 0129 — Kyiv
- Local Institution - 0132 — Poltava
- Local Institution - 0137 — Ternopil
Аргентина · 5 центров
- Hospital Italiano de Buenos Aires — ABB
- Clinica del Prado — Las Heras
- Sanatorio Morra S.A. — Córdoba
- Local Institution - 0109 — Mendoza
- Local Institution - 0140 — Santiago del Estero
Венгрия · 3 центра
- Petz Aladar Egyetemi Oktato Korhaz — Győr
- Semmelweis Egyetem — Budapest
- Local Institution - 0114 — Budapest
Австралия · 2 центра
- Ramsay Clinic Northside — St Leonards
- Ramsay Clinic New Farm — Brisbane
Новая Зеландия · 1 центр
- North Shore Hospital — Auckland
Идентификаторы
NCT: NCT06951698 · CN012-0036 · 2024-520165-32 · U1111-1316-7438