Phase 3 Schizophrenia Trial, Recruiting NCT07606014 Sponsor: University Medical Center Groningen Condition: Schizophrenia
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Phase 3 Schizophrenia Trial, Recruiting

NCT07606014
Recruiting Phase 3

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who are about to start, or who have started within the last 8 weeks, taking one of these antipsychotic medications for psychosis: olanzapine, quetiapine (at a full therapeutic dose, not a low dose used only as a sleep aid), clozapine, or risperidone
  • People aged between 18 and 65 years old
  • People who have not used any of these four antipsychotic medications for more than one week in a row during the past 6 months (not counting the current medication if it was started within the last 8 weeks)
  • People who understand the study and are able to sign a written consent form

Who may not be able to join:

  • People who are critically ill (for example, currently in an intensive care unit), or who have been diagnosed with an eating disorder, a long-term gut or digestive condition, a liver or pancreas disorder, diabetes, or metabolic syndrome
  • People currently taking medications that affect metabolism or weight (such as diabetes medications or GLP-1 medications), proton pump inhibitors, diuretics, or beta blockers, or who have taken antibiotics or probiotic supplements (such as Yakult, Activia, or similar products containing large numbers of live bacteria) in the past 4 weeks
  • People who are pregnant or breastfeeding
  • People who, in the treating doctor's judgment, would be unable to follow the study requirements or have other conditions that might affect the study results (confirm with trial site)

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 13 July 2026
Phase 3: approximately ~65% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Iris E.C. Sommer, Prof. Dr., University Medical Center Groningen

Phone: +31681528283

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 3
Registry
ClinicalTrials.gov
Start date
1 June 2026
Est. completion
1 May 2029

Where this trial is recruiting

🇳🇱 Netherlands

Primary endpoints

Hemoglobin A1C

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 13 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov