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A Study of ONO-1110 in Patients With Social Anxiety Disorder

A Study of ONO-1110 in Patients With Social Anxiety Disorder

Recruiting
18-65 years
All
Phase 2

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Overview

To Evaluate the Efficacy and Safety of ONO-1110 in Patients with Social Anxiety Disorder

Eligibility

Inclusion Criteria:

  1. Japanese participants (sex not specified)
  2. Participants who, in the opinion of the principal (or sub-investigator), are capable of understanding the content of the clinical trial and complying with its requirements
  3. Participants diagnosed with social anxiety disorder based on DSM-5-TR (Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, Text Revision) criteria, as determined through an interview using the M.I.N.I. (Mini-international neuropsychiatric interview)
  4. Outpatients
  5. Participants with a LSAS-J (Liebowitz Social Anxiety Scale Japanese version) total score of 70 or higher and a CGI-S (Clinical global impression-Severity) score of 4 or higher

Exclusion Criteria:

  1. Participants with a current or past history of psychiatric or neurological disorders that meet any of the following criteria:
    • Participants with a comorbid psychiatric disorder other than social anxiety disorder as defined by DSM-5-TR (Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, Text Revision) (assessed using the M.I.N.I. (Mini-international neuropsychiatric interview))
    • Participants with a comorbid or past history of schizophrenia or other psychotic disorders as defined by DSM-5-TR (Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, Text Revision)
    • Participants with neurodevelopmental disorders, neurocognitive disorders, or personality disorders (excluding avoidant personality disorder) as defined by DSM-5-TR
  2. Participants who have been primarily diagnosed with a disorder other than social

    anxiety disorder according to DSM-5-TR (Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, Text Revision) criteria within 24 weeks prior to screening

  3. Participants with a MADRS (Montgomery Åsberg Depression Rating Scale) total score of 15 or higher
  4. Participants who, in the opinion of the principal (or sub-investigator), have not responded to at least two different SSRIs (Selective serotonin reuptake inhibitor), each administered at an adequate dose for at least 10 weeks, in treating social anxiety disorder

Study details
    Social Anxiety Disorder (SAD)

NCT06805565

Ono Pharmaceutical Co. Ltd

15 October 2025

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