ALTO-300 in Depression (ALTO-300-004)

Last updated: April 24, 2024
Sponsor: Alto Neuroscience
Overall Status: Completed

Phase

2

Condition

Affective Disorders

Depression (Major/severe)

Depression

Treatment

ALTO-300 PO Tablet

Clinical Study ID

NCT05157945
ALTO-300-004
  • Ages 18-74
  • All Genders

Study Summary

The purpose of this study is to collect biologically-based data for defining predictors and correlates of the effects of ALTO-300.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Have a diagnosis of moderate to severe major depressive disorder
  • Currently taking a SSRI, SNRI, or bupropion for at least 6 weeks with no dosemodifications in the past 2 weeks
  • Must have failed to adequately respond to the current antidepressant medication
  • Willing to comply with all study assessments and procedures
  • Must not be pregnant or breastfeeding at time of enrollment or throughout study

Exclusion

Exclusion Criteria:

  • Evidence of liver impairment or disease
  • Active suicidal ideation
  • Moderate to severe Alcohol Use Disorder
  • Diagnosed bipolar disorder or psychotic disorder
  • Has a history of hypersensitivity or allergic reaction to ALTO-300 or any of itscomponents/excipients
  • Concurrent or recent participation in another clinical trial for mental illnessinvolving an investigational product or device

Study Design

Total Participants: 148
Treatment Group(s): 1
Primary Treatment: ALTO-300 PO Tablet
Phase: 2
Study Start date:
February 03, 2022
Estimated Completion Date:
May 05, 2023

Connect with a study center

  • Cerebral - Atlanta

    Atlanta, Georgia 30324
    United States

    Site Not Available

  • Site 171

    Jackson, Mississippi 39216
    United States

    Site Not Available

  • Cerebral - New York City

    New York, New York 10013
    United States

    Site Not Available

  • Cerebral - Dallas

    Dallas, Texas 75212
    United States

    Site Not Available

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