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ALTO-207 in Adults With Treatment-resistant Depression (TRD)

RecruitingPhase 2

A Randomized, Double-blind, Placebo-controlled Trial of ALTO-207 in Adults With Treatment-resistant Depression

Who can join

Ages 18 to 75 · All sexes

Full eligibility criteria
Inclusion Criteria:

* Male and female participants, ages 18 to 75 years, inclusive, at the time of signing the ICF.
* Prior diagnosis of MDD without psychotic symptoms (in the current episode) and have confirmatory diagnosis of current MDD (moderate to severe).
* Failure to respond (\<50% improvement) to at least 2-5 antidepressant treatments (including the current treatment)
* Currently taking a stable dose of at least 1 but no more than 2 oral antidepressants at baseline

Exclusion Criteria:

* Evidence of unstable medical condition
* Concurrent use of any prohibited medications or substance use disorder
* Diagnosed bipolar disorder or a psychotic disorder or symptoms
* Significant current PTSD symptoms or history of PTSD
* Clinically significant current impulse control difficulties
* Has a history of hypersensitivity or allergic reaction to ALTO-207 or any of its components/excipients
* Concurrent or recent participation in another clinical trial for mental illness involving an investigational product or device

About the study

The purpose of this trial is to measure depressive symptoms following treatment with ALTO-207 compared with placebo in participants with TRD.

What is being tested

Sponsor: Alto Neuroscience · Participants: 178 · Started: May 20, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07553637

Locations in the U.S.

AlabamaSite 7173, Dothan
ArizonaSite 7000, Phoenix
CaliforniaSite 7153, Chino
Site 7195, La Jolla (Not yet recruiting)
Site 7069, Los Angeles
Site 7156, Oakland
Site 7082, Oceanside
Site 7159, Palo Alto (Not yet recruiting)
Site 7016, Sacramento
Site 7144, San Diego
Site 7120, San Jose
Site 7171, Valley Village
ConnecticutSite 7200, Wilton (Not yet recruiting)
FloridaSite 7152, Saint Augustine
GeorgiaSite 7148, Albany
Site 7146, Marietta
Site 7141, Savannah
Site 7064, Snellville
IllinoisSite 7192, Naperville
IndianaSite 7169, Indianapolis
MarylandSite 7185, Baltimore (Not yet recruiting)
Site 7054, Pikesville
Site 7180, Rockville
MassachusettsSite 7166, Worcester
MichiganSite 7155, Ann Arbor
Site 7154, Bloomfield Hills
Site 7178, Grand Rapids (Not yet recruiting)
MissouriSite 7189, St Louis
New JerseySite 7066, Toms River
New YorkSite 7170, Amherst
Site 7055, Cedarhurst
Site 7162, Lewiston
Site 7157, Syracuse
North CarolinaSite 7127, Cary
Site 7143, Charlotte
OhioSite 7029, Cincinnati
Site 7194, Dayton (Not yet recruiting)
Site 7158, Garfield Heights
Rhode IslandSite 7172, East Providence
South CarolinaSite 7191, North Myrtle Beach (Not yet recruiting)
TexasSite 7199, Austin (Not yet recruiting)
Site 7190, Bryan (Not yet recruiting)
Site 7176, Dallas
Site 7160, Fort Worth
Site 7150, Galveston (Not yet recruiting)
Site 7145, Houston
Site 7175, Houston
Site 7161, Irving
Site 7186, Plano
VirginiaSite 7177, Fairfax
West VirginiaSite 7163, South Charleston (Not yet recruiting)

Conditions

From ClinicalTrials.gov, data retrieved Nov 15, 2026. Each study sets its own eligibility; the study team decides who can join.