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RECRUITINGPhase 2INTERVENTIONAL

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

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

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

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.

Who May Be Eligible (Plain English)

Who May Qualify: - 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 Who Should NOT Join This Trial: - 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 Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
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

Treatments Being Tested

DRUG

ALTO-100

ALTO-100 40 mg tablet BID

DRUG

Placebo

Placebo tablet BID

Locations (20)

Site 6036
Chandler, Arizona, United States
Site 6000
Phoenix, Arizona, United States
Site 6087
Yuma, Arizona, United States
6039
Fayetteville, Arkansas, United States
6070
Little Rock, Arkansas, United States
Site 6081
Imperial, California, United States
6069
Los Angeles, California, United States
Site 6016
Mather, California, United States
Site 6082
Oceanside, California, United States
Site 6102
Riverside, California, United States
Site 6112
Colorado Springs, Colorado, United States
Site 6067
Lauderhill, Florida, United States
Site 6068
Atlanta, Georgia, United States
Site 6064
Peachtree Corners, Georgia, United States
Site 6151
Baltimore, Maryland, United States
Site 6076
Bel Air, Maryland, United States
Site 6062
Gaithersburg, Maryland, United States
Site 6142
Lincoln, Nebraska, United States
Site 6144
Las Vegas, Nevada, United States
Site 6104
Las Vegas, Nevada, United States