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Study of ALTO-300 in MDD

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NCT05922878 · readout ≤ 134 d

Sponsored by Alto Neuroscience (industry) · ANRO — their whole pipeline →.

Phase
Phase 2
Status
Recruiting
Study type
Interventional
Design
Randomized · Quadruple · Treatment
Enrollment
321estimated
Sites
45
Country
United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2023-06-08actualWhen the study began enrolling
Primary completionDec 2026estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionDec 2026estimatedThe whole study's end, after follow-up
First posted2023-06-28actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-07-24actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Major Depressive Disorder

Interventions

  • Drug: ALTO-300
  • Drug: Placebo

Primary outcome

what the primary-completion date above is the date OF
To assess efficacy of adjunctive ALTO-300 versus placebo on symptoms of MDD in a pre-defined subgroup of participants as measured by the change over time up to week 6 in the Montgomery-Åsberg Depression Rating Scale (MADRS).
measured Change over time for up to week 6

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