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ALTO-100 in Bipolar Disorder With Depression (BD-D)

RecruitingPhase 2

A Randomized, Double-Blind, Placebo-Controlled Study Followed by Open-Label Treatment of ALTO-100 in Adults With Bipolar Disorder Currently Experiencing a Major Depressive Episode

Who can join

Ages 18 to 70 · All sexes

Full eligibility criteria
Inclusion Criteria:

* Have a diagnosis of BD-I or BD-II as well as BD-D
* At baseline, taking a mood stabilizer, lithium (LI) or lamotrigine (LMG) or valproic acid (VPA, any form) or combination of Li + LMG or Li + VPA and/or taking an approved atypical antipsychotic medication (olanzapine, quetiapine, lurasidone, risperidone, ziprasidone, cariprazine, aripiprazole, lumateperone, and asenapine) for at least 6 weeks with no dose modifications in the past 2 weeks
* Willing to comply with all study assessments and procedures
* Must not be pregnant or breastfeeding at time of enrollment or throughout study

Exclusion Criteria:

* Evidence of unstable medical condition
* Concurrent use of any prohibited medications or substance use disorder
* Diagnosed psychotic disorder (other than mania or depression)
* Current moderate or severe substance use disorder
* Has a history of hypersensitivity or allergic reaction to ALTO-100 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 study is to assess antidepressant efficacy differences between ALTO-100 and placebo during the Double-Blind period in patients with bipolar disorder I or II with current major depressive episode, when used adjunctively to a mood stabilizer and/or atypical antipsychotic, related to patient characteristics. Additionally, safety, tolerability, and efficacy will be assessed in a subsequent open label treatment period.

What is being tested

Sponsor: Alto Neuroscience · Participants: 200 · Started: Oct 2, 2024

Contact the study team

Official record on ClinicalTrials.gov — NCT06656416

Locations in the U.S.

ArizonaSite 6000, Phoenix
Site 6087, Yuma
Arkansas6039, Fayetteville
6070, Little Rock
CaliforniaSite 6081, Imperial
6069, Los Angeles
Site 6016, Mather (Not yet recruiting)
Site 6082, Oceanside
Site 6102, Riverside
ColoradoSite 6112, Colorado Springs (Not yet recruiting)
GeorgiaSite 6068, Atlanta
Site 6064, Peachtree Corners
MarylandSite 6076, Bel Air
Site 6062, Gaithersburg
NebraskaSite 6142, Lincoln
NevadaSite 6104, Las Vegas
Site 6144, Las Vegas
New JerseySite 6066, Toms River
New MexicoSite 6014, Albuquerque (Not yet recruiting)
Site 6078, Albuquerque
Ohio6065, North Canton
Site 6075, Westlake
TexasSite 6072, Houston
UtahSite 6121, Draper (Not yet recruiting)

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.