INTERVENTIONALAuthorised2024-518608-28-00
Effect of tirzepatide on alcohol intake and reward processing in patients diagnosed with schizophrenia and alcohol use disorder
This study will examine the effects of tirzepatide vs. placebo on alcohol consumption in patients diagnosed with schizophrenia and alcohol use disorder.
Locally preserved from EU Clinical Trials Information SystemOpen EU Clinical Trials Information System↗last source update 2026-01-08
What this record can show
Protocol only - no registry results posted
This locally preserved record separates the registered protocol from source-reported registry results. Neither is a treatment recommendation.
Registry facts
Study at a glance
- Phase
- PHASEII
- Enrollment
- 108 (ACTUAL OR ANTICIPATED)
- Start date
- 2025-05-01
- Sponsor
- Psykiatrisk Center Kobenhavn
- Design
- Not reported
- Locations
- 0
- Results record
- Not present in registry snapshot
This trial is carried out for exploration of new indication for an existing product that already has a marketing authorisation.
Schizophrenia and Alcohol Use DisorderSchizophrenia and Alcohol Use Disorder
Linked local records
Related local records
Local links use governed condition terms or exact source-reported intervention names. They are navigation candidates, not efficacy claims.
Cannabinoids and active compounds
No governed compound link was found.
Medicines
No exact medicine-name link was found.
Interventions
What was registered
No structured intervention was reported.
Eligibility
Population and criteria
- Sex
- Not reported
- Minimum age
- Not reported
- Maximum age
- Not reported
- Healthy volunteers
- Not reported
Eligibility criteria
- ['Informed Consent: The patient must provide both oral and written informed consent.', 'Diagnosis: o Diagnosed with alcohol dependence according to the International Classification of Diseases, 10th Edition (ICD-10), and alcohol use disorder as per the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5). o Diagnosed with schizophrenia spectrum disorder according to ICD-10 and DSM-5', 'AUDIT Score: Alcohol Use Disorder Identification Test (AUDIT) score greater than 15.', 'Body Mass Index (BMI): BMI of 23 kg/m² or higher.', 'Age Range: Between 18 and 70 years old (inclusive).', 'Heavy Alcohol Consumption: Defined as 4 or more heavy drinking days within a consecutive 21-day period during the 28 days preceding the baseline evaluation. The 21-day period will be selected based on the largest total alcohol consumption and the greatest number of heavy drinking days within the 28-day timeframe. This will be assessed using the Timeline Followback (TLFB) method. Heavy drinking days are defined as days with an alcohol intake of 4 or more units (48 g of alcohol) for women and 5 or more units (60 g of alcohol) for men.'] ['- Intellectual Disability: individuals with a diagnosis of intellectual disability.', '- Liver Function: Impaired hepatic function, defined as liver transaminases greater than three times the upper limit of normal.', '- Renal Function: Impaired renal function, indicated by an estimated glomerular filtration rate (eGFR) below 50 mL/min and/or plasma creatinine above 150 μmol/L.', '- Pancreatic Function: History of acute or chronic pancreatitis or amylase levels more than twice the upper limit of normal.', '- Thyroid Conditions: Previous medullary thyroid carcinoma (MTC) or a family history of MTC and/or Multiple Endocrine Neoplasia syndrome type 2 (MEN 2).', '- Cardiac Issues: Decompensated heart failure (NYHA class III or IV), unstable angina pectoris, or myocardial infarction within the past 12 months.', '- Uncontrolled Hypertension: Systolic blood pressure above 180 mmHg or diastolic blood pressure above 110 mmHg.', '- Alcohol Use Disorder Medication: Use of medications for alcohol use disorder (e.g., disulfiram, naltrexone, acamprosate, nalmefene) within the 28 days prior to inclusion as recorded in the Timeline Followback (TLFB) schedule.', '- Investigational Drugs: Receipt of any investigational drug within the past three months.', '- Weight-Lowering Medications: Use of other weight-lowering pharmacotherapy, including tirzepatide or other GLP-1 RA, in the past three months.', '- Allergic Reactions: Hypersensitivity to the active substance or any of the excipients.', '- Acute Psychosis: Acute exacerbation of psychosis, Severe acute exacerbation of psychosis, as assessed by the investigator during clinical evaluation', '- Language Barriers: Inability to speak and/or understand Danish.', "- Other Conditions: Any other condition that, in the investigator's opinion, may interfere with participation in the trial.", 'For the subgroup of participants undergoing brain scans: - MRI Contraindications: any contraindications for MRI (e.g., magnetic implants, pacemaker, claustrophobia). - Benzodiazepine Use: Intermittent use of benzodiazepines within 12 days prior to the scanning session is not allowed. However, regular use of a stable dose of benzodiazepines is permitted.', '- Coercive Measures: Current use of coercive measures, which includes individuals sentenced to treatment (‘dom til behandling’).', '- Suicidal Behaviour: Evidence of current severe suicidal behaviour, as assessed by the investigator during clinical evaluation.', '- History of Severe Alcohol Withdrawal: History of delirium tremens or alcohol withdrawal seizures.', '- Severe Withdrawal Symptoms: Clinical Institute Withdrawal Assessment of Alcohol Scale, revised (CIWA-Ar) score greater than 9 at baseline examination.', '- Severe Neurological Conditions: Presence of severe neurological diseases, including severe traumatic brain injury.', '- Diabetes: Type 1 or 2 diabetes', '- Pregnant or potentially pregnant women: Women of childbearing potential (WOCBP) who are pregnant, breastfeeding, intend to become pregnant within the next eight months (including 26 weeks of treatment plus two months after discontinuation of tirzepatide), or are not using a highly effective contraceptive method throughout the study period. Highly effective methods include combined hormonal contraception (oral, intravaginal, transdermal), progestogen-only hormonal contraception (oral, injectable, implantable), intrauterine device (IUD), intrauterine system (IUS), bilateral tubal occlusion, vasectomised partner, or sexual abstinence. WOCBP with a measured serum human chorionic gonadotropin (hCG) level greater than 3 U/L at inclusion will also be excluded']
Publications
Locally readable linked articles
0No exact PMID-linked public article is currently readable locally.
Snapshot provenance
- Snapshot
- bda8416a-75a9-4663-8888-21de6fd760b6
- Retrieved
- 25/08/2026, 17:02:27
- SHA-256
- 033988bdf86145cff6501549dc642fc1e1712e3abb64fa5e39f6b1b47a26b30f