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NCT06969755RecruitingPhase 4

Biomarkers to Enhance Early Schizophrenia Treatment

Source: ClinicalTrials.gov · Last updated 31 Jul 2026

Brief summary (registry, in English)

This study is recruiting participants who are experiencing a first episode of psychosis and who have certain genetic factors that may make them respond better to certain medications that are used to treat people with psychosis.

Status (registry)
Recruiting
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
180 (estimated)
First submitted
4 Apr 2025
Start date
4 Sept 2024
Primary completion date
30 Jul 2030
Lead sponsor
Northwell Health
NCT number
NCT06969755

What you commit to

  • Study type: Interventional · Phase 4
  • Planned participants: 180
  • From 4 Sept 2024 to the primary completion date, 30 Jul 2030
  • 5 sites in 2 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Any medical condition which requires treatment with a medication with psychotropic effects.
  • Meeting SCID-5 substance use disorder moderate or severe for any substance, other than nicotine within 3 months of screening visit. Meeting SCID5 substance use disorder mild for any substance other than cannabis, alcohol, or nicotine for less than 3 months prior to screening visit, or a positive urine baseline drug screen with a substance other than nicotine, alcohol, or cannabis
  • Prior psychosurgery

Other illness

  • The patient reports or medical records state a serious neurological or endocrine disorder at screening that the investigator determines could interfere with the interpretation of the efficacy or safety measurements
  • Seizure disorder (self-report)
    • \-

Other

  • An abnormal EKG at screening that the investigator determines could interfere with the interpretation of the efficacy or safety measurements
  • Significant risk of suicidal or homicidal behavior (i.e. 'severe' risk on the Columbia Suicide Scale, a 'hostility' score of 7 on the BPRS, or an answer of 'yes' on questions 4,5 or 6 on the CDSS).
  • Cognitive limitations, or any other factor that would preclude potential participants providing informed consent
  • Contraindications to MRI (e.g. pacemaker).
  • Suspected DSM5 intellectual disability based upon clinical interview and psychosocial history, as well as screening with the Weschler Test for Adult Reading (IQ score \<71)
  • Pregnancy (self-report)

Who the study is looking for

  • Aged 18 to 35.
  • DSM5 diagnosis (as determined by the SCID5) of schizophrenia, schizoaffective disorder, schizophreniform disorder.
  • Current positive symptoms rated ≥4 (moderate) on one or more of the following BPRS positive subscale items: unusual thought content, conceptual disorganization, hallucinatory behavior, suspiciousness.
  • Preserved striatal connectivity, as determined by screening MRI scan
  • Absence of the MC4R high-risk genotype, as determined by genetic testing
  • Absence of the HLA-DQB1 high-risk genotype, as determined by genetic testing
  • In an early phase of illness as defined by having taken antipsychotic drugs for a cumulative lifetime period of 4 weeks or less (with exceptions of very low doses for other off-label indications, e.g. sleep)
  • Ability to provide informed consent

Age in the registry: 18 years to 35 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (5)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Centre for Addiction and Mental Health
Coordinator of this site? Confirm its status
TorontoCanadaRecruiting
McLean
Coordinator of this site? Confirm its status
BelmontUnited StatesRecruiting
The University of Alabama at Birmingham
Coordinator of this site? Confirm its status
BirminghamUnited StatesRecruiting
Feinstein Institute for Medical Research
Coordinator of this site? Confirm its status
Glen OaksUnited StatesRecruiting
University of California San Diego
Coordinator of this site? Confirm its status
La JollaUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.