drugset / Trial / NCT07065240

A Study to Evaluate the Efficacy and Safety of SPT-300 (GlyphAllo) in Participants With Major Depressive Disorder, With or Without Anxious Distress (BUOY-1 Study)

NCT07065240 ↗

Phase 2 Recruiting 360 enrolled Seaport Therapeutics Premier Research · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a randomized, parallel-group, double-blind, placebo-controlled, monotherapy study to evaluate the efficacy, safety, and tolerability of SPT-300 (GlyphAllo) in adults with major depressive disorder (MDD), with or without anxious distress.

Timeline

Start
2025-06-19
Primary completion
2027-03
Completion
2027-03

Drugs

EvaluationDrugModalityDoseRoute
Subject SPT-300 Small molecule — —