A Study to Assess Efficacy and Safety of KarXT for the Treatment of Psychosis Associated With Alzheimer's Disease (ADEPT-2)
A legfontosabb adatok
- Hol
- Calgary, Hamilton, Montreal, Toronto, Verdun és Whitby (Kanada)Mind a 6 helyszín megnézése
- Fázis
- 3. fázis
AI-kivonat: kiket keres a vizsgálat
A vizsgálat saját részvételi feltételeiből. Gép olvasta ki az oldalon álló regiszterszövegből, ezért tévedhet. Hogy ki vehet részt, azt a lenti regiszterszöveg és a vizsgálat csapata dönti el.
A vizsgálat 55 és 90 év közötti, enyhe vagy súlyos Alzheimer-kórban szenvedő embereket keres, akiknél a betegség miatt közepesen súlyos vagy súlyos pszichózis (hallucinációk vagy téveszmék) is van.
- Életkor
- 55 és 90 év között
- Nem
- Férfiak és nők
- A betegség stádiuma
- Lehetséges vagy valószínű Alzheimer-kór, legalább 2 hónapja fennálló hallucinációkkal vagy téveszmékkel. Memóriateszt (MMSE) eredménye 8 és 22 között.
- Korábbi kezelés
- Korábban nem kaphatott KarXT-t. A szűrés előtti 3 hónapban nem szedhetett kísérleti gyógyszert.
A részvétel fő kizáró okai
- Olyan pszichózis, amelyet főként nem az Alzheimer-kór okoz
- Bipoláris zavar, skizofrénia vagy skizoaffektív zavar a kórtörténetben
- Pszichotikus tünetekkel járó súlyos depresszió az elmúlt 12 hónapban
- Vizeletretenció, gyomorretenció vagy szűkzugú glaukóma a kórtörténetben vagy nagy kockázata
- Trospium-klorid vagy a KarXT összetevői iránti túlérzékenység, vagy súlyos mellékhatás trospium miatt
Gépi kiolvasás: 2026. november 12.
Neked szólhat?
Magadról válaszolj. Ez nem döntés: hogy részt vehetsz-e, azt csak a vizsgálat csapata mondhatja meg.
- 55 és 90 év között vagy?
- Has a doctor told you that you have Alzheimer's disease?
- Do you have hallucinations or delusions caused by Alzheimer's disease?
- Have you taken part in an earlier study of the same medicine (KarXT or ML-007C-MA) and finished it?
- Has a doctor ever told you that you have bipolar disorder, schizophrenia or schizoaffective disorder?
Forrás: NCT06126224: ki vehet részt
Helyszínek itt: Kanada
- Calgary, AlbertaHospital not named in the registryNo longer taking part
- Hamilton, OntarioHospital not named in the registryNo longer taking part
- Montreal, QuebecHospital not named in the registryNo longer taking part
- Toronto, OntarioHospital not named in the registryNo longer taking part
- Verdun, QuebecHospital not named in the registryNo longer taking part
- Whitby, OntarioHospital not named in the registryNo longer taking part
Kérdések a vizsgálat csapatának
- Milyen gyakran kell bejárnom, és egy-egy alkalom mennyi ideig tart?
- Megtérítik az utazási költséget?
- Megtarthatom a saját orvosomat?
- Mi történik, ha ki akarok lépni?
Contact the study team: see the registry record → Contacts and Locations
Oldal nyomtatása az orvosomnakA vizsgálat adatai
- Ki végzi
- Karuna Therapeutics, Inc., a Bristol Myers Squibb company
- Azonosító
- NCT06126224EU 2023-504416-16-00
- A regiszteradat frissítve
- 2026. október 16.
- Eredeti leírás
This is a Phase 3, randomized, double-blind, placebo-controlled, parallel group study to evaluate the safety and efficacy of KarXT in male and female subjects who are aged 55 to 90 years and have mild to severe Alzheimer's Disease (AD) with moderate to severe psychosis related to AD.A teljes eredeti leírásKevesebb
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Evaluate the Safety and Efficacy of KarXT for the Treatment of Psychosis Associated With Alzheimer's Disease
This is a Phase 3, randomized, double-blind, placebo-controlled, parallel group study to evaluate the safety and efficacy of KarXT in male and female subjects who are aged 55 to 90 years and have mild to severe Alzheimer's Disease (AD) with moderate to severe psychosis related to AD.
The primary objective of the study is to evaluate the efficacy of KarXT compared with placebo in the treatment of subjects with psychosis associated with AD as measured by the Neuropsychiatric Inventory-Clinician (NPI-C): Hallucinations and Delusions (H+D) score.
Bevonási feltételek: Is a male or female aged 55 to 90 years, inclusive, at Screening; Can understand the nature of the trial and protocol requirements and provide informed consent or assent before any study assessments are performed; Meets clinical criteria for Possible AD or Probable AD; Must have a magnetic resonance imaging (MRI) or computed tomography (CT) scan of the brain (completed within the past 5 years) taken during or subsequent to the onset of dementia to rule out other central nervous system (CNS) disease that could account for the dementia syndrome, e.g., major stroke, neoplasm, subdural hematoma. If not available, a non-contrast brain MRI or non-contrast head CT must be done during Screening; Living at the same home or residential assisted-living facility for a minimum of 6 weeks before Screening; Have an identified study partner who should have daily contact (approximately 10 hours a week or more); History of psychotic symptoms (meeting International Psychogeriatric Association criteria) (Cummings 2020) for at least 2 months prior to Screening; CGI-S scale with a score ≥ 4 at Screening and Baseline; AD subjects are required to have NPI-C: Hallucinations and Delusions (H+D) score of ≥ 6 AND meet at least 1 of the following criteria at Screening and Baseline:; Moderate to severe delusions, defined as NPI-C: Delusions domain score of ≥ 2 on 2 of the 8 items OR; Moderate to severe hallucinations, defined as NPI-C: Hallucinations domain score of ≥ 2 on 2 of the 7 items; MMSE score of 8 to 22, inclusive, at Screening.
Kizáró feltételek: History of major depressive episode with psychotic features during the 12 months prior to Screening; Prior exposure to KarXT; Participation in another clinical study in which the subject received an experimental or investigational drug within 3 months before Screening or has participated in more than 2 clinical studies in the 12 months prior to Screening; Psychotic symptoms that are primarily attributable to a condition other than the AD causing the dementia; History of bipolar disorder, schizophrenia, or schizoaffective disorder; Significant or severe medical conditions including pulmonary, hepatic, renal, hematologic, gastrointestinal, endocrine, immunologic, dermatologic, neurologic, cardiovascular, or oncologic disease or any other condition that, in the opinion of the Investigator, could jeopardize the safety of the subject, ability to complete or comply with the study procedures or validity of the study results; History of hypersensitivity to KarXT excipients or trospium chloride; History or high risk of urinary retention, gastric retention, or narrow-angle glaucoma as evaluated by the Investigator; Experienced any significant adverse events (AEs) due to trospium; Other protocol-defined inclusion/exclusion criteria may apply.