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NCT Number: NCT06482554

Lumateperone for the Improvement of Apathy in Patients With Psychotic Symptoms.

This study is looking to determine if Lumateperone improves motivation in patients with schizophrenia or schizoaffective disorders who show high levels of apathy as judged by AES-C-Apathy (Apathy Evaluation Scale - Clinician - Apathy) assessment and to examine a possible correlation between improvement in apathy scores and changes in elements of the PANSS (Positive and Negative Syndrome Scale) due to treatment with Lumateperone.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

About this study

  • To determine if Lumateperone improves motivation in patients with schizophrenia or schizoaffective disorders who show high levels of apathy as judged by AES-C-Apathy assessment.
  • To examine a possible correlation between improvement in apathy scores and changes in elements of the PANSS (Positive and Negative Syndrome Scale) due to treatment with Lumateperone.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male or female subjects between the ages of 18-65 that have been diagnosed with Schizophrenia, Schizoaffective Disorder or Schizophrenia Spectrum and Other Psychotic Disorders.
  • A BPRS score > 35 at the screening visit.
  • An AES-C score > 32 at the screening visit.
  • If the subject is on a therapeutic regimen, that regimen must be stable for at least 30 days prior to screening. A therapeutic regimen may include medication, supplements, and/or probiotics.
  • In the opinion of the Investigator, the subject is able to participate in all scheduled evaluations, and likely to be compliant and complete all required assessments.
  • Female subjects of childbearing potential must not be pregnant or breast-feeding. Female subjects of childbearing potential must have a negative urine pregnancy test. Subjects of childbearing or child-fathering potential must be willing to use medically acceptable forms of birth control, which includes abstinence, while being treated on this study and for 30 days after the last dose of study drug.
  • Must speak and understand English, as the consent and all evaluations will be conducted in English.
  • Must be willing to take and pass a urine drug screen with a negative result in order to rule out psychotic symptoms due to drugs of abuse.

Exclusion criteria

  • A BPRS score < 35 at the screening visit.
  • An AES-C score < 32 at the screening visit.
  • Have any clinically significant medical condition or an unstable intercurrent illness that would, in the opinion of the Investigator, preclude study participation.
  • Are currently taking more than one antipsychotic medication.
  • Are currently taking a long-acting injectable medication for psychotic symptoms.
  • Have a substance use disorder or show a positive drug screen for stimulants.
  • Are pregnant or of female sex with no evidence of measures for pregnancy prevention.
  • Presence of dementia.
  • Intellectual disability or cognitive impairment that would affect the symptom/apathy assessments, in the view of the investigator.
  • A diagnosis of Parkinson's disease.

Treatment and study plan

Lumateperone 42 mg

Drug

Standard treatment with lumateperone

Other names: Lumateperone

Risperidone 2 mg

Drug

Standard treatment with other antipsychotic drugs

Other names: olanzapine; quetiapine; ziprasidone; aripiprazole

Primary outcomes

  1. Change in AES-C Score

    Time frame: 8 weeks

    Difference between the mean change in the AES-C score from baseline (V1) to Week 8 (V3) for 42 mg/day lumateperone vs. current antipsychotic medication.

Secondary outcomes

  1. Change in PANSS Score

    Time frame: 8 weeks

    Difference between the mean change in the PANSS score from baseline (V1) to Week 8 (V3) for 42 mg/day lumateperone vs. current antipsychotic medication.

  2. Change in BPRS Score

    Time frame: 8 weeks

    Difference between the mean change in the BPRS (Brief Psychiatric Rating Scale) score from baseline (V1) to Week 8 (V3) for 42 mg/day lumateperone vs. current antipsychotic medication.

  3. Correlations between AES-C and PANSS Scores

    Time frame: 8 weeks

    Correlation between the AES-C score at Week 8 (V3) and negative symptoms score from PANSS at Week 8 (V3) for 42 mg/day lumateperone in comparison to current antipsychotic medication.

Study contacts

Contact information is provided by the study sponsor or research team.

Shawn McNeil, MD

CONTACT

[email protected]

318-675-7065

Stephanie Saunders, MA, CCRC

CONTACT

[email protected]

318-675-7065

Sponsors and collaborators

Lead sponsor

Louisiana State University Health Sciences Center Shreveport

Other

Registry information

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Jul 1, 2024
Registry last updated
Jul 1, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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