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Taking peoplePhase 2

Tests ALTO-207 against placebo in adults with treatment-resistant depression

Tests whether ALTO-207 affects depression symptoms in adults with treatment-resistant depression.

Plain-language title generated from the registry record
Registry title: ALTO-207 in Adults With Treatment-resistant Depression (TRD)

Key facts

Where
Antrim, Birmingham, Bristol, Cardiff, Exeter, London, Nottingham, Oxford, Prescot, and Sheffield, United KingdomSee the 10 sites
Phase
Phase 2

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 75 years old?

Source: NCT07553637, who can take part

Where in United Kingdom

  • AntrimAntrim, United KingdomNot yet recruiting
  • BirminghamBirmingham, United KingdomNot yet recruiting
  • BristolBristol, United KingdomNot yet recruiting
  • CardiffCardiff, United KingdomNot yet recruiting
  • ExeterExeter, United KingdomNot yet recruiting
  • LondonLondon, United KingdomNot yet recruiting
  • NottinghamNottingham, United KingdomNot yet recruiting
  • OxfordOxford, United KingdomNot yet recruiting
  • PrescotPrescot, United KingdomNot yet recruiting
  • SheffieldSheffield, United KingdomNot yet recruiting

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Alto Neuroscience
Trial code
NCT07553637
Record updated
26 October 2026
Original description
The purpose of this trial is to measure depressive symptoms following treatment with ALTO-207 compared with placebo in participants with TRD.Read full original descriptionShow less

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

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

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

ClinicalTrials.gov NCT07553637