Study of KarXT (trospium chloride and xanomeline tartrate) and KarX-EC (xanomeline tartrate) for cognitive impairment in mild to moderate Alzheimer’s disease

3 1

What is this study about?

This study aims to test the effectiveness of medications called KarXT and KarX-EC in treating thinking and memory problems in people with Alzheimer’s Disease. These medications contain active substances called trospium chloride and xanomeline tartrate, which are taken as capsules by mouth.

The study will involve people with mild to moderate Alzheimer’s Disease, who will receive either the study medications or placebo for 24 weeks. The medications are being tested to see if they can help improve cognitive function (thinking abilities) and daily functioning in people with Alzheimer’s Disease.

During the study, participants will take the medication daily and attend regular check-ups where their mental abilities and overall condition will be assessed. The study will track any changes in participants’ ability to think, perform daily activities, and their overall health status. Healthcare providers will monitor participants’ safety throughout the study period.

1 Initial screening

You will undergo screening to confirm if you meet the study requirements for mild to moderate Alzheimer’s Disease

Your thinking abilities will be tested using the MMSE test (a standard memory and thinking assessment). Your score should be between 12 and 22

You must be between 60 and 85 years old to participate

You need to have a caregiver who spends at least 10 hours per week with you and can attend all study visits

2 Medication requirements check

If you are currently taking memory medications (AChEIs and/or memantine), you must have been on a stable dose for at least 12 weeks

You will need to maintain this same dose throughout the study

3 Treatment period

The study will last 24 weeks (approximately 6 months)

You will receive either KarXT + KarX-EC capsules or placebo capsules (inactive treatment)

The medication will be taken by mouth

Your caregiver will help ensure you take the medication as prescribed

4 Monitoring and assessments

Your thinking abilities will be tested regularly using the ADAS-Cog11 test

Your daily activities will be assessed using the ADCS-ADL assessment

Your behavior will be evaluated using the NPI assessment

Regular health checks will include vital signs, heart tests (ECG), weight measurements, and laboratory tests

Any side effects or health changes will be monitored throughout the study

5 Final assessment

At week 24, final assessments will be conducted to measure changes in your thinking abilities and overall function

Your caregiver will provide information about changes in your daily activities and behavior

Who Can Join the Study?

  • Must be between 60 and 85 years old, both men and women can participate
  • Must have a MMSE score between 12 and 22 during screening (MMSE is a simple test that checks memory and thinking skills)
  • Must have a dedicated caregiver who:
    • Spends at least 10 hours per week with the participant
    • Can attend all study visits
    • Will help monitor the participant’s condition
    • Will help with taking medications
    • Will ensure study procedures are followed
  • If currently taking memory medications (AChEIs and/or memantine):
    • Must have been on the same dose for at least 12 weeks before screening
    • Must agree to stay on the same dose throughout the study

Who Cannot Join the Study?

  • History of severe allergic reactions or sensitivity to similar medications
  • Current diagnosis of major psychiatric disorders (such as schizophrenia, bipolar disorder, or severe depression)
  • Significant heart problems or uncontrolled high blood pressure
  • Severe liver or kidney disease
  • History of seizures or other neurological conditions besides Alzheimer’s Disease
  • Current use of medications that could interact with the study drug
  • Participation in another clinical trial within the past 30 days
  • Inability to follow study procedures or attend regular visits
  • Substance abuse within the past year
  • Dementia caused by conditions other than Alzheimer’s Disease
  • Severe vitamin B12 or folate deficiency
  • History of stroke or transient ischemic attack (temporary stroke-like symptoms) in the past 6 months
  • Unstable medical conditions that could interfere with the study
  • Presence of any medical devices that would prevent brain imaging if needed

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Other Sites

Site Name City Country Status
Diagnostic & Therapeutic Center Of Athens Hygeia Single Member S.A. Athens Greece
Centre Hospitalier Universitaire De Nantes Nantes France
Hopital Beaujon Clichy France
University Of Eastern Finland Kuopio Finland
Fundacio Ace Institut Catala De Neurociencies Aplicades Barcelona Spain
Brain Research Center Zwolle B.V. Zwolle The Netherlands
Unidade Local De Saude Do Alto Ave E.P.E. Guimaraes Portugal
Hqynaawt Uqgzqdyehhyjel Pkchz Sgcukxhjfmu Paris France
Uzikevymxt Gejeztu Hbgrfkcj Og Tktgeszbaofp Ajnpg Thessaloniki Greece
Uhrreqlyan Hpfemhhy Cedseac Cologne Germany
Amhkpoagha Pgvzgykp Hbovgdwz Dl Mxnlqlqkn Marseille France
Cxhqlc Hbtacrzkjsi Rbziozvj Uiincuttcosjd Du Twonf Tours France
Cqtdtr Htmebygfsw E Utvwochaqdsun Dl Cxmhysk Epmtxg Coimbra Portugal
Atqxjik Owknpgahicq Ujntnbbtzubcb Fnuzvlnu Il Dj Npicto Naples Italy
Cupk Dz Npwcb Vandoeuvre Les Nancy France
Gipzzqd Uzryakjqjv Hjdhaqxt Ot Pkvygk Patras Greece
Acsmtcr Ozczkigmggn Uxjrxsznkhjpt Otpnaipk Rswfarj Foggia Italy
Kfjzygmp dlp Ufeimcactlys Mlaqvyzb Adt Munich Germany
Chwxcz Hbmqtmcucad Ubvrampyrzdgf Dl Riyplg Rennes France
Cpdjct Hvmhyiysue Uppxushxeanjf Dt Smoue Atamlmo Ejztqh Porto Portugal
Iaubptli fcdj Kxbevhoeo Tnilrblqrovriufuiqe uzr Izxymosqjvxd Uvo gsekj Ulm Germany
Cyjsjt Hqobgsmiwib Lrnq Sjs Pierre Benite France
Hzdnedzr Ucsbkldmglwwx 1k Dn Opsduwe Madrid Spain
Hyrynduz Uxwezckyannie Mtpqtsj Dv Vzghnioydr Santander Spain
Ctmm Cnbjss Chtyamd Axxdnobft Bstzu Arirwuhxse Braga Portugal
Hgslgcne Ungwanjdjsvjba Sbmiztmmup &fyrkxa Hmuebfh ds Hemkipgxvue STRASBOURG, Alsace France
Uavktainpt Gviolqx Hspmouvl Awkefvq Gxhnjqo Hpdrtegj Ov Wwnm Aoxivx H Aykd Vvmsxdg Chaidari Greece
Bnugl Rlnwjatk Cmzztm Dmr Bzmfc Bwmm S-Hertogenbosch The Netherlands
Sewdefsj Czmmnl Dx Pzauosjrmo Sr Nwbkqqkzgf Betzey Brasov Romania
Ela Sppqxkf Sft z ouvo Katowice Poland
Iykskqbl Zvudfvs Da Bblrokshizhpftrdy Oświęcim Poland
Bktcplyf Cwszke Seuook Constanta Romania
Psowl Hddwtyliu Prvojnakcnq Wroclaw Poland
Hcbtvlbe Uwnjluuwamdph Qfcxyjgbdnt Mmisdq Pozuelo De Alarcon Spain
Hyejttvy Rqjgp Joqj Bqude Madrid Spain
Stdppjuf Uskbrzxwlpk Ds Ultnzqn Mayrwyj Cewpaqt Diw Calow Dtgucm Bucharest Romania
Ciupapgj Rjiiyjdy Seuvorno Tghgy Crrk Oh Turku Finland
Hoitzgqu Uifovpiigwarn De Pjrdr Aezutplnhk Valencia Spain
Cdho Hkcbzybt Od Helsinki Finland
Pdeahbxzmzz Gwkeogms Saya Donostia / San Sebastian Spain
Bzqfa Riooctlf Cjdije Aloczngkk Bhnx Amsterdam The Netherlands
Uhdbmjp Leqin Di Slyrh Df Mhvoglbteb Eontdu Senhora Da Hora Portugal
Cyg Ssmsr Ldiy Torres Vedras Portugal
Zqigbvj frua kzrwkdhhs Fgrgrmcxm Dxh It Sjigysb Gshh Bad Homburg Germany
Snnzdz Tnowhfbjczo Oj Turku Finland

Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
Finland Finland
Recruiting
25.07.2025
France France
Recruiting
25.07.2025
Germany Germany
Recruiting
25.07.2025
Greece Greece
Recruiting
25.07.2025
Italy Italy
Recruiting
25.07.2025
Poland Poland
Recruiting
25.07.2025
Portugal Portugal
Recruiting
25.07.2025
Romania Romania
Recruiting
25.07.2025
Spain Spain
Recruiting
25.07.2025
The Netherlands The Netherlands
Recruiting
25.07.2025

Trial locations

KarXT is an investigational medication being studied for treating cognitive impairment (problems with thinking and memory) in people who have mild to moderate Alzheimer’s disease. It works by targeting specific brain receptors that are involved in cognitive function.

KarX-EC is a complementary medication being studied alongside KarXT. Together, these medications are being tested to see if they can help improve thinking abilities and daily functioning in people with Alzheimer’s disease.

Investigated Diseases:

Alzheimer’s Disease – A progressive brain disorder that gradually destroys memory, thinking skills, and the ability to carry out simple tasks. The disease begins with mild memory loss and confusion, which slowly becomes more severe over time. In mild to moderate stages, people experience increasing problems with memory, planning, language, and spatial awareness. The condition affects the parts of the brain that control thought, memory, and language. During these stages, individuals may have difficulty remembering recent events, following conversations, and managing daily activities. Changes in mood and personality may also occur, with some people becoming anxious, suspicious, or easily upset.

Trial ID:
2025-520747-32-00
Protocol code:
CN012-0052
NCT ID:
NCT06976203
Trial Phase:
Therapeutic confirmatory (Phase III)

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