The Role of Glutamatergic Function in the Pathophysiology of Treatment-resistant Schizophrenia

NCT ID: NCT06270108

Last Updated: 2024-03-05

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: EARLY_PHASE1
• Total Enrollment: 288 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-11-14
• Study Completion Date: 2024-12-31

Brief Summary

The goal of this basic science study is to to explore the responsivity of glutamate in the brain of treatment-resistant schizophrenia patients to the drug riluzole. The main aims of the study are:

To assess the role of glutamate in treatment-resistant schizophrenia using magnetic resonance spectroscopy.

To assess the relationship between glutamate levels and brain structural and functional measures (using: structural MRI; functional MRI (fMRI) and arterial spin labelling (ASL)) at baseline.

To assess the relationship between longitudinal change in glutamate levels and brain structural and functional measures.

To assess the relationship between longitudinal change in glutamate levels and changes in psychopathology.

The researchers will compare the changes with healthy controls and those without treatment-resistant schizophrenia.

Conditions

Treatment-resistant Schizophrenia; Treatment-responsive Schizophrenia; Healthy Controls

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: NONE

Study Groups

Treatment-resistant schizophrenia patients receiving riluzole

Group Type: EXPERIMENTAL

Riluzole

Intervention Type: DRUG

50mg twice daily (100mg total daily) for 56 days.

Treatment-responsive schizophrenia patients

Group Type: NO_INTERVENTION

No interventions assigned to this group

Healthy controls

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

Riluzole

50mg twice daily (100mg total daily) for 56 days.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Aged 18 years old or older;

2. Diagnosis of schizophrenia or other psychotic disorder (Diagnostic and Statistical Manual of Mental Disorders-5 (DSM-5);

3. Treatment resistance according to the Treatment Response and Resistance in Psychosis (TRRIP) Working Group consensus criteria. This requires a PANSS score of more than 70 and the presence of at least one positive and one negative symptom rated as ≥ 4 on the Positive and Negative Syndrome Scale (PANSS) and at least moderate functional impairment on the Social and Occupational Function Assessment Scale (SOFAS) despite at least 2 adequate trials of different antipsychotics;

4. On a stable dose of antipsychotic (no dose changes in the past 1 month);

5. Able to give fully informed written consent and likely to comply with the requirements of the study, after reading the information and consent form, and after having the opportunity to discuss the study with the investigator or his delegate;

6. Capacity to provide informed consent, as judged by an investigator and as assessed by the McArthur scale;

7. Ability to communicate satisfactorily with the investigator and to participate in, and comply with the requirements of the entire study.

1. Aged 18 years old or older;

2. Diagnosis of schizophrenia or other psychotic disorder (Diagnostic and Statistical Manual of Mental Disorders-5 (DSM-5);

3. On a stable dose of antipsychotic (no dose changes in the past 1 month);

4. Able to give fully informed written consent and likely to comply with the requirements of the study, after reading the information and consent form, and after having the opportunity to discuss the study with the investigator or his delegate;

5. Capacity to provide informed consent, as judged by an investigator and as assessed by the McArthur scale;

6. Ability to communicate satisfactorily with the investigator and to participate in, and comply with the requirements of the entire study.

1. Aged 18 years old or older;

2. No diagnosis of schizophrenia, schizophreniform or any psychotic disorder;

3. Sufficient understanding of the nature of the study and any hazards of participating in it;

4. Ability to communicate satisfactorily with the investigator and to participate in, and comply with the requirements of the entire study;

5. Willingness to give written consent to participate after reading the information and consent form, and after having the opportunity to discuss the study with the investigator or his delegate;

6. Capacity to provide informed consent, as judged by an investigator.

Exclusion Criteria

1. History of significant co-morbid central nervous system (CNS) disorder (including significant head trauma or significant loss of consciousness, Parkinson's Disease, Epilepsy, Alzheimer's Dementia, Huntington's Disease);

2. Current use of medication with recognized effect on glutamatergic signaling (e.g. lamotrigine, lithium, carbamazepine, opiates, and psychostimulants) OR medication that is known to interact with riluzole (eg: ciprofloxacin, combined hormonal contraceptives, enoxacin, fluvoxamine, charcoal boiled (grilled) foods, methoxasalen, rucaparib, osilodrostat, mexiletine, nicergoline, pipemidic acid, rifampicin, tiabendazole, vemurafenib);

3. Any absolute contra-indication to riluzole according to the British National Formulary (such as interstitial lung disease, current pregnancy or lactation, severe hepatic impairment liver function tests more than 3x Upper limit of normal, acute porphyria, pancreatitis);

4. Pregnancy and/or breast-feeding;

5. Substance dependence/abuse other than to cigarettes;

6. Current high suicide risk or other significant safety risk as judged by the patient's psychiatrist or study physician;

7. Current homicidal ideation or intent;

8. Participation in a clinical study of unlicensed medicines within the previous 30 days;

9. Clinically relevant abnormal findings at the screening assessment as judged significant by the principal investigator (e.g.: history of liver disease or transaminases more than 2 times the upper limit of normal);

10. Presence of other acute or chronic illness or history of chronic illness sufficient to invalidate the volunteer's participation in the study or raise safety concerns;

11. Any risk factors for liver damage (eg. alcohol dependence or history of liver disease) or patients who are receiving potentially hepatotoxic medications;

12. Likelihood that the subject will not comply with study requirements or other reason the investigator judges the subject is not suitable;

13. Objection by subject's physician;

14. Any contraindication to MRI scanning (e.g. metallic implants);

15. Any comorbidity that could compromise scanning safety (e.g. severe asthma).

1. Treatment resistance according to the Treatment Response and Resistance in Psychosis (TRRIP) Working Group consensus criteria;

2. History of significant co-morbid CNS disorder (including significant head trauma or significant loss of consciousness, Parkinson's Disease, Epilepsy, Alzheimer's Dementia, Huntington's Disease);

3. Substance dependence/abuse other than to cigarettes;

4. Current high suicide risk or other significant safety risk as judged by the patient's psychiatrist or study physician;

5. Current homicidal ideation or intent;

6. Participation in a clinical study of unlicensed medicines within the previous 30 days;

7. Likelihood that the subject will not comply with study requirements or other reason the investigator judges the subject is not suitable;

8. Objection by subject's physician;

9. Any contraindication to MRI scanning (e.g. metallic implants);

10. Any comorbidity that could compromise scanning safety (e.g. severe asthma);

1. Co-morbid psychiatric or other CNS disorder;

2. Family history of Schizophrenia or Psychotic disorders;

3. History of head trauma or loss of consciousness;

4. Substance dependence/abuse other than to cigarettes;

5. Presence of acute or chronic illness or history of chronic illness sufficient to invalidate the volunteer's participation in the study or make it unnecessarily hazardous and judge significant by the principal investigator;

6. Likelihood that the volunteer will not comply with the requirements of the study or other reason the investigator judges the subject is not suitable;

7. Objection by a General Practitioner (GP), or another doctor responsible for their treatment, to the healthy control entering study.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

South London and Maudsley NHS Foundation Trust

OTHER

Sponsor Role: collaborator

King's College London

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Oliver D Howes

Role: PRINCIPAL_INVESTIGATOR

King's College London

Locations

Institute of Psychiatry, Psychology and Neuroscience

London, , United Kingdom

Site Status: RECRUITING

Countries

United Kingdom

Central Contacts

James Scott

Role: CONTACT

james.1.scott@kcl.ac.uk

+44 207 848 0002

Guy Gitlin-Leigh

Role: CONTACT

guy.1.gitlin-leigh@kcl.ac.uk

Facility Contacts

James Scott

Role: primary

james.1.scott@kcl.ac.uk

+44 207 848 0002

Guy Gitlin-Leigh

Role: backup

guy.1.gitlin-leigh@kcl.ac.uk

Other Identifiers

299382

Identifier Type: OTHER

Identifier Source: secondary_id

22/SS/0040

Identifier Type: -

Identifier Source: org_study_id