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Single dose of LSD formulation improves anxiety in Phase 2b trial

The Brown University Psychopharmacology Update November 28, 2025 DOI: 10.1002/pu.31394 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Phase 2b clinical trial Peer reviewed
Population Individuals with generalized anxiety disorder (GAD)
Topics Anxiety LSD
Keywords Phase matter Drug Pharmacology Anesthesia Clinical trial
Key findings The two highest dose strengths of MM120 (LSD formulation) produced significant dose-dependent reductions in anxiety relative to placebo.

Abstract

Treatment with a single dose of a pharmaceutical formulation of lysergic acid diethylamide (LSD) resulted in a dose‐dependent reduction in anxiety in individuals with generalized anxiety disorder (GAD), a Phase 2b study has found. The two highest of four tested dose strengths of the MM120 formulation demonstrated significant improvement relative to placebo.

In the evidence

This study is part of the evidence base for a synthesis in the library. Here is how each one recorded it.

  • The two highest dose strengths of an LSD formulation produced significant dose-dependent reductions in anxiety relative to placebo.

    Synthesized

Comparable studies

Other non-randomized and open-label trials on LSD for anxiety, most cited first.

Study Year Design Participants
SHORT-TERM EFFECTS OF LSD ON ANXIETY, ATTITUDES AND PERFORMANCE Normal adults, mostly professional research personnel 1964 Controlled trial n = 29
LSD microdosing in major depressive disorder: results from an open-label trial Participants with major depressive disorder, most taking antidepressant medication 2025 Open-label phase 2A trial n = 19
Evaluating the Potential of Microdosing 1cp-LSD for the Treatment of Canine Anxiety: A One-Month Case Study. A 13-year-old female dog with severe separation anxiety 2025 Pilot study, single-case study n = 1
MedCheck: Psilocybin for Depression, LSD for Anxiety, Donanemab, LSD, and More Patients with moderate to severe major depressive disorder 2024 Phase 2 clinical trial n = 34

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