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Completed

NCT Number: NCT02978599

Clinical Trial of AVL-3288 in Schizophrenia Patients

Single-center, outpatient, randomized, double-blind, placebo-controlled, 3-treatment-phase, cross-over study to evaluate the safety, tolerability and efficacy of two oral doses of AVL-3288 each compared to placebo, in patients with schizophrenia.

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Key information

Age range

18 year–50 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

New York State Psychiatric Institute

New York, 10032, United States

About this study

This study will be in 24 non-smoking outpatients with schizophrenia or schizoaffective disorder. Subjects will complete three treatment phases, each involving 5 straight days of taking AVL-3288 (10 mg or 30 mg study drug or placebo) followed by a 16 day washout period in which subjects do not take the study drug to ensure that the drug is completed eliminated from the body before the next phase.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • DSM-V diagnosis of schizophrenia or schizoaffective disorder
  • RBANS Total Scale Score >62
  • Willing to provide informed consent
  • Medically stable for study participation
  • Taking an antipsychotic medication other than clozapine at a stable dose for at least 4 weeks
  • Judged clinically not to be at significant suicide or violence risk

Exclusion criteria

  • Substance abuse (excluding nicotine) within last 90 days
  • ECG abnormality that is clinically significant
  • Current clozapine use
  • Participation in a study of investigational medication/device within 4 weeks
  • Pregnancy, lactation, or lack of use of effective birth control
  • Active tobacco use
  • Presence or positive history of significant medical or neurological illness, including cardiac illness, WBC <3500/mm3, absolute neutrophil count <1500/mm3, ALT or AST values >1.5 times upper limit of normal. Hemoglobin less than 130 g/L (13 g/dL) in males or 120 g/L (12 g/dL) in females or known HIV +
  • Contraindication to MRI scanning, including metal implants or claustrophobia
  • Medicinal patch, unless removed

Treatment and study plan

AVL-3288

Drug

daily for 5 days

Other names: Anvylic-3288

Placebo

Drug

daily for 5 days

Primary outcomes

  1. Repeatable Battery for the Assessment of Neuropsychological Status (RBANS) Total Scale Score

    Time frame: End of each 5-day treatment phase

    Compare effect of active drug (AVL-3288) to placebo on RBANS total score

Secondary outcomes

  1. RBANS index T-score subscales

    Time frame: End of each 5-day treatment phase

    Compare effect of active drug (AVL-3288) to placebo on RBANS index T-score subscales

  2. Brief Psychiatric Rating Scale (BPRS) Total score

    Time frame: End of each 5-day treatment phase

    Compare effect of active drug (AVL-3288) to placebo on BPRS Total Score.

  3. Calgary Depression Rating Scale (CDRS) Total score

    Time frame: End of each 5-day treatment phase

    Compare effect of active drug (AVL-3288) to placebo on CDRS Total Score.

  4. Scale for the Assessment of Negative Symptoms (SANS) Total score

    Time frame: End of each 5-day treatment phase

    Compare effect of active drug (AVL-3288) to placebo on SANS Total score

  5. P50 suppression measured by electroencephalographic (EEG)

    Time frame: End of each 5-day treatment phase

    Compare P50 suppression measured by EEG between active drug (AVL-3288) and placebo

  6. Intensity of hippocampal BOLD fMRI signal during MRI scan

    Time frame: end of each 5-day treatment phase

    Compare intensity of Hippocampal BOLD signal between active drug (AVL-3288) and placebo

Sponsors and collaborators

Lead sponsor

New York State Psychiatric Institute

Other

Collaborators

  • National Institute of Mental Health (NIMH)

Registry information

Official study title

Double Blind, Two Dose, Cross-over Clinical Trial of the Positive Allosteric Modulator at the alpha7 Nicotinic Cholinergic Receptor AVL-3288 in Schizophrenia Patients

Important dates

Study start
2016
Primary completion
2018
Study completion
2018
First posted
Dec 1, 2016
Registry last updated
Jan 22, 2019

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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