Around 300 million people worldwide are affected by a variety of mental health conditions that microdosing may address.

Microdosing

Microdosing involves the regular consumption of sub-hallucinogenic doses of psychedelics, primarily for cognitive enhancement and emotional wellbeing. Although popularised through anecdotal reports, rigorous scientific evidence on its effects is still limited, pointing to a critical need for further research in this emerging field.

Key Insights

  • 1

    Microdosing has gained popularity, particularly among young professionals, for perceived benefits in mental health and cognitive performance.

  • 2

    Self-reported data indicates that microdosing may be associated with lower prevalence of substance use disorders and anxiety among users.

  • 3

    Preliminary studies suggest microdosing may significantly impact symptoms of ADHD, offering a potential alternative to conventional medications.

  • 4

    Current research highlights the need for controlled clinical trials to validate the anecdotal benefits and safety of microdosing practices.

  • 5

    The placebo effect may play a significant role in reported outcomes of microdosing, necessitating further investigation.

What is Microdosing?

Microdosing refers to the use of low doses of psychedelic substances, typically below the threshold of perceptual effects, administered over multiple sessions with the intention of enhancing cognitive and emotional processes.

The most commonly reported substances used in microdosing are LSD and psilocybin, which are often taken on a specific schedule, such as one day on followed by two days off.

Anecdotal reports suggest benefits such as improved mental wellbeing, increased focus, and enhanced creativity; however, these claims require substantiation through scientifically rigorous methodologies.

Lack of robust clinical trials has resulted in microdosing being predominantly studied through self-reported measures, such as surveys, raising concerns about the reliability of the findings.

Current Treatments

Standard treatments for conditions like ADHD and anxiety currently include pharmacological approaches such as stimulants and SSRIs, along with behavioural therapies. These interventions, while effective, may not work for all individuals and can present side effects.

Psychedelic Effect Matrix

Compound efficacy and evidence levels for Microdosing.

CompoundMagnitudeEvidenceConsistency
LSD
Evidence primarily derived from self-reported surveys, with few clinical studies completed.
MediumModerateInconsistent
Psilocybin
Similar to LSD, relies on self-reported outcomes with limited controlled studies thus far.
MediumModerateInconsistent

LSD and Microdosing

LSD is known for its profound psychological effects, even at microdose levels. Users report enhanced cognitive flexibility, improved mood, and heightened creativity, although scientific validation of these claims is sparse. Preliminary findings suggest microdosing LSD may facilitate neural plasticity, which could have implications for cognitive enhancement in daily activities.

Psilocybin and Microdosing

Microdoses of psilocybin may assist in emotional regulation and cognitive improvement, according to anecdotal accounts. Early observational studies indicate that psilocybin could help alleviate symptoms related to anxiety and depression, potentially shifting the neurochemical balance towards a more positive emotional state, yet the need for controlled trials remains critical to ascertain these effects.

Industrial Landscape

Key players in the microdosing space include Woke Pharmaceuticals, which is developing novel psychedelic compounds, and MindBio Therapeutics, conducting clinical research on microdosing for various mental health conditions. Notable researchers like Vince Polito from Macquarie University are also contributing to the scientific exploration of microdosing effects.

Quick Indicators

Prevalence
Around 300 million people worldwide are affected by a variety of mental health conditions that microdosing may address.
Trials
13
Papers
129

Key Organizations

12

Janssen Research & Development

Janssen Research & Development is the pharmaceutical research and development arm of Johnson & Johnson (J&J). Operating under J&J's Innovative Medicine division, Janssen has sponsored clinical trials into ketamine-derived compounds, including esketamine (Spravato), the first FDA-approved psychedelic-adjacent treatment for treatment-resistant depression.

Algernon Pharmaceuticals

Algernon Pharmaceuticals (also known as Algernon Health / Algernon NeuroScience) is the first company in the world to test DMT as an emergent treatment for ischemic stroke and traumatic brain injury. Their lead candidate AP-188 uses sub-hallucinogenic IV DMT to promote neuroplasticity and neuroprotection. Phase 1 completed at the Centre for Human Drug Research in Leiden; Phase 2a stroke trial planned.

Clexio Biosciences

Clexio Biosciences is a private Israeli clinical-stage CNS company founded in 2018 by Teva Pharmaceuticals R&D veterans. Their lead programme CLE-100 is a once-daily oral tablet formulation of esketamine for MDD — distinguished from the FDA-approved Spravato (intranasal, in-clinic) by enabling outpatient, at-home use. Phase 2 CLEO study results showed a promising safety profile and encouraging efficacy specifically in post-COVID MDD subgroups; the Phase 2 SOLEO study (NCT06340958, higher dose, stricter treatment-resistance criteria) enrolled first patients April 2024 and reached 50% enrollment by December 2024. CLE-100 holds multiple US method-of-use patents (2024). In December 2025, Clexio spun out its muscarinic agonist programme (CLE-905) into a new entity, Syremis Therapeutics, which raised $165M Series A co-led by Dexcel Pharma and Third Rock Ventures. Co-founders Kogan, Levy, and Kagan simultaneously lead Syremis; Clexio continues independently with CLE-100 and preclinical CLE-043.

OPEN Foundation

The OPEN Foundation is a Dutch non-profit organisation that advances psychedelic research and therapy through scientific conferences, interdisciplinary research, clinician training, and public education. It organises events (including the ICPR conference), runs research and training programmes, and advocates for ethical integration of psychedelics into healthcare in the Netherlands and Europe.

Clerkenwell Health

Clerkenwell Health (trading as Clerkenwell Clinics Limited) is a UK-based clinical research organisation that designs and runs psychiatry and central nervous system (CNS) clinical trials and provides psychedelic-assisted therapy services. It operates specialist clinics and site networks to support early-phase CNS and mental-health research.

Exeter University

The University of Exeter is a public research university based in Exeter, Devon, England, with additional campuses in Cornwall. It provides undergraduate and postgraduate education and conducts research across a wide range of disciplines.

Cybin

Cybin Inc. (founded 2019) is a Canadian clinical-stage biopharmaceutical company developing psychedelic-based therapeutics—now operating as Helus Pharma—focused on proprietary novel serotonergic agonists and deuterated psilocin analogs for mental health conditions.

Ohio State University

The Ohio State University is a public land-grant research university based in Columbus, Ohio, offering undergraduate, graduate, and professional programs and conducting research across many fields. It was founded as the Ohio Agricultural and Mechanical College and serves as a major educational and economic institution in Ohio.

COMPASS Pathways

COMPASS Pathways is a UK-listed biopharmaceutical company developing COMP360 synthetic psilocybin therapy for treatment-resistant depression, with two successful Phase 3 trials making it the leading candidate for the first regulatory approval of a classic psychedelic medicine.

Diamond Therapeutics

Diamond Therapeutics is a private Canadian clinical-stage company pioneering sub-perceptual (non-hallucinogenic) psilocybin therapy. Their approach focuses on low-dose psilocybin that does not produce psychedelic experiences, enabling at-home outpatient administration — a differentiated strategy from the clinic-based, high-dose psychedelic-assisted therapy model. Founded in 2018 by CEO Judith Blumstock, Diamond completed a Phase 1 single ascending dose study in healthy volunteers (n=56, 7 cohorts, December 2022) establishing a safe non-hallucinogenic dose range. Their Phase 2a GAD programme received Health Canada approval in January 2023 — the first Health Canada NOL for a psychedelic trial in GAD — and enrolled first patients at Kingston Health Sciences Centre in 2025 in the first-ever at-home microdose psilocybin study. A parallel FDA-authorized Phase 2 demoralization trial is also underway at UAB. Diamond is funded by private investors and non-dilutive public grants, including a $1.1M+ CQDM/Brain Canada drug discovery consortium launched in May 2025.

Definium Therapeutics

Definium Therapeutics (formerly Mind Medicine / MindMed) is a late-stage clinical biopharmaceutical company headquartered in New York, founded in 2019 and rebranded in January 2026. Led by CEO Robert Barrow, the company applies scientific rigor to psychedelic-derived molecules to develop accessible, rapidly-acting psychiatric treatments. Its lead asset, DT120 ODT (formerly MM-120) — a pharmaceutically optimised formulation of lysergide D-tartrate (LSD) as an orally disintegrating tablet — has received FDA Breakthrough Therapy Designation for generalised anxiety disorder (GAD) and delivered compelling Phase 2b results: 65% clinical response rate and 48% remission at 12 weeks following a single dose. Three Phase 3 trials are currently underway: Voyage and Panorama (GAD) and Emerge (MDD, fully enrolled). Topline data from all three studies is expected in 2026, potentially positioning Definium for the first-ever FDA approval of an LSD-derived therapy. A second pipeline asset, DT402 (formerly MM402) — an MDMA-related compound — is in Phase 1 development for autism spectrum disorder.

Lobe Sciences

Canadian psychedelic biotech developing conjugated psilocin formulations for treatment-resistant conditions. Spun out its proprietary Conjugated Psilocin™ technology to Cynaptec Pharmaceuticals in April 2025 via an $8.46 million financing round. Lead programme L-130 targets cluster headache disorder.

Prominent Researchers

4

Connected Evidence

The latest clinical data and verified academic findings associated with Microdosing.

Academic Research

All papers