LSD microdosing for major depressive disorder: Mood and pharmacokinetic outcomes from a Phase 2a trial
Dimitri Henriques Daldegan-Bueno, C Donegan, Rachael Sumner, Anna Forsyth, Soo Hee Jeong, William Evans, Malak Alshakhouri, Robin J Murphy, Lisa Reynolds, Nicholas Hoeh, Nathan Allen, Frederick Sundram, David B Menkes, Suresh Muthukumaraswamy
Progress in Neuro-psychopharmacology and Biological Psychiatry February 18, 2026 DOI: 10.1016/j.pnpbp.2026.111645 (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | Clinical trial Peer reviewed |
|---|---|
| Population | People with depression |
| Intervention | LSD |
| Dose | 8 μg |
| Topics | Depression LSD Microdosing |
| Keywords | Pharmacokinetics Depression economics Depressive symptoms Clinical trial Sample material Clinical psychology Pharmacology Depressive mood Phase matter |
| Citations | 1 |
| Key findings | Short-term mood improvements followed microdosed LSD in people with depression, with no tolerance or sensitisation observed despite dose titration. |
Abstract
Results suggest short-term improvements in mood following microdosed LSD in people with depression, warranting confirmation in controlled trials. It provides the pharmacokinetic parameters of 8 μg of LSD in a sample of people with depression and indicates no tolerance or sensitisation to repeated microdoses of LSD, despite incremental dose titration.
In the evidence
This study is part of the evidence base for 2 syntheses in the library. Here is how each one recorded it.
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Short-term mood improvements followed microdosed LSD (8 μg) in people with depression, with no tolerance or sensitisation observed despite dose titration.
Synthesized
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Short-term improvements in mood followed microdosed LSD in people with depression, with no tolerance or sensitisation observed.
Synthesized
Comparable studies
Other non-randomized and open-label trials on LSD and microdosing, most cited first.