Compound tracker

DMT.

A source-backed research page for trial rows and update notes connected to this compound or investigational product. The page is generated from the Notion tracker and should be read as a living research map, not a medical conclusion.

27 trial rows 4 update rows Latest checked: May 15, 2026 All trials
Claim boundary

Trial registration, company topline, CNPV/rolling-review status, recruitment status, public-dashboard data, or review literature do not equal approval, label, reimbursement, access, safety, or efficacy. Related update rows are shown only when they include visible Last checked text and an explicit Claim boundary.

Backlinks

This page links out to registry/source records, the global trial tracker, the updates feed, and matching wiki dossiers when available.

27
Trial rows
N/A / Phase 1 / Phase 1/2 / Phase 2
Phases tracked
Active / Active not recruiting / Completed
Statuses seen
NCT07540494 Phase 1 Not yet recruiting updated Apr 14, 2026

Pharmacokinetics and Safety of GH001 Delivered Via a GH001 Aerosol Delivery System in Healthy Subjects

Condition
Healthy Adult
Sponsor / institution
GH Research Ireland Limited
Start date
Apr 1, 2026
Tracker note / source boundary

ClinicalTrials.gov v2 verification on 2026-04-24 | Overall status: NOT_YET_RECRUITING | Exact phase: PHASE1 | Lead sponsor: GH Research Ireland Limited | Conditions: Healthy Adult | Interventions: DRUG: 5 Methoxy N,N Dimethyltryptamine; DEVICE: GH001 Aerosol Delivery System | Registry start date type: ESTIMATED (2026-04).

NCT06927076 N/A Recruiting updated Apr 2, 2026

Antidepressant Response of DMT Masked With Propofol

Condition
Major Depressive Disorder, Psychedelic Experiences
Sponsor / institution
University Hospital, Basel, Switzerland
Start date
Aug 5, 2025
Tracker note / source boundary

ClinicalTrials.gov v2 sync on 2026-04-18 | Overall status: RECRUITING | Exact phase: NA | Lead sponsor: University Hospital, Basel, Switzerland | Conditions: Major Depressive Disorder; Psychedelic Experiences | Interventions: N,N-Dimethyltryptamine; Placebo; Propofol; no sedation

NCT07444788 Phase 1 Recruiting updated Feb 24, 2026

Acute Effects of Intravenous 5-MeO-DMT in Healthy Participants

Condition
Healthy Participants
Sponsor / institution
University Hospital, Basel, Switzerland
Start date
Mar 31, 2026
Tracker note / source boundary

ClinicalTrials.gov v2 verification on 2026-04-24 | Overall status: RECRUITING | Exact phase: PHASE1 | Lead sponsor: University Hospital, Basel, Switzerland | Conditions: 5-methoxy-dimethyltryptamine (5-MeO-DMT) | Interventions: DRUG: 0.2 mg/min 5-MeO-DMT; DRUG: 0.4 mg/min 5-MeO-DMT; DRUG: 0.6 mg/min 5-MeO-DMT; DRUG: 0.8 mg/min 5-MeO-DMT; DRUG: Placebo | Registry start date type: ESTIMATED (2026-03-31).

NCT06051721 Phase 2 Active not recruiting updated Oct 27, 2025

HLP004 / CYB004 deuterated DMT analog Phase 2 for generalized anxiety disorder

Condition
Generalized Anxiety Disorder
Sponsor / institution
Cybin IRL Limited / Helus Pharma
Start date
May 10, 2024
Tracker note / source boundary

Last checked 2026-05-16 UTC. Claim boundary: registry and company-source backfill only; active-not-recruiting Phase 2 status and company topline claims do not establish approval, label, reimbursement, access, independent efficacy confirmation, broad safety, or Phase 3 success. Registry: randomized quadruple-masked active-controlled Phase 2a in GAD; estimated n=36; two CYB004 medicine sessions ~3 weeks apart plus EMBARK psychotherapy; primary outcome HAM-A across Day 364; actual primary completion 2025-10-14.

NCT06810765 Phase 2 Stopped updated Aug 22, 2025

Trifecta Research Study: Examining Hormone Replacement Therapy, Magnetic e-Resonance Therapy, Ibogaine, and 5-MeO-DMT in the Treatment of Posttraumatic Stress Disorder and Traumatic Brain Injury-related Cognitive Symptoms

Condition
PTSD - Post Traumatic Stress Disorder; Cognitive Dysfunction; Brain Trauma; Brain Injuries
Sponsor / institution
Johns Hopkins University
Start date
Tracker note / source boundary

ClinicalTrials.gov manual QA on 2026-04-17 | Exact registry status: Withdrawn | Official title: Trifecta Research Study: Examining Hormone Replacement Therapy, Magnetic e-Resonance Therapy, Ibogaine, and 5-MeO-DMT in the Treatment of Posttraumatic Stress Disorder and Traumatic Brain Injury-related Cognitive Symptoms | Sponsor: Johns Hopkins University | Conditions: PTSD - Post Traumatic Stress Disorder; Cognitive Dysfunction; Brain Trauma; Brain Injuries | Interventions: Hormone Replacement Therapy (HRT); Magnetic Resonance Therapy (MeRT); ibogaine with magnesium treatment; 5-MeO-DMT | Study type: Interventional

NCT05870540 Phase 2 Completed updated Jul 17, 2025

BPL-003 Efficacy and Safety in Treatment Resistant Depression

Condition
Treatment Resistant Depression
Sponsor / institution
Beckley Psytech Limited
Start date
Sep 14, 2023
Tracker note / source boundary

ClinicalTrials.gov v2 verification on 2026-04-24 | Overall status: COMPLETED | Exact phase: PHASE2 | Lead sponsor: Beckley Psytech Limited | Conditions: Treatment Resistant Depression | Interventions: DRUG: BPL-003; DRUG: BPL-003 | Asset identity checked against atai/Beckley 2025-10-16 source: BPL-003 is intranasal mebufotenin (5-MeO-DMT) benzoate.

NCT05800860 Phase 2 Completed updated May 31, 2025

A Trial of GH001 in Patients With Treatment-resistant Depression

Condition
Treatment-resistant Depression
Sponsor / institution
GH Research Ireland Limited
Start date
May 24, 2023
Tracker note / source boundary

ClinicalTrials.gov v2 sync on 2026-04-10 | Overall status: COMPLETED | Exact phase: Phase 2 | Lead sponsor: GH Research Ireland Limited | Conditions: Treatment-resistant Depression

NCT05695495 Phase 1 Completed updated Apr 11, 2025

Acute Dose-dependent Effects of DMT-bolus Applications in Healthy Subjects (DMT BDR-Study) (DMT BDR)

Condition
Healthy
Sponsor / institution
University Hospital, Basel, Switzerland
Start date
Jun 12, 2024
Tracker note / source boundary

ClinicalTrials.gov manual QA on 2026-04-17 | Status: Completed | Sponsor: University Hospital, Basel, Switzerland | Official title: Acute Dose-dependent Effects of DMT-bolus Applications in Healthy Subjects: A Placebo-controlled Cross-over Study (DMT BDR-Study) | Condition: Healthy | Intervention: N,N-Dimethyltryptamine bolus dose arms plus placebo | Study type: Interventional | Official title: Acute Dose-dependent Effects of DMT-bolus Applications in Healthy Subjects: A Placebo-controlled Cross-over Study (DMT BDR-Study).

NCT06812221 Phase 1/2 Completed updated Apr 9, 2025

Efficacy of Sublingual 5-MeO-DMT for Reducing Anxiety and Depression in MCI (5-MeO-DMT)

Condition
Mild Cognitive Impairment; Anxiety State; Depression Anxiety Disorder
Sponsor / institution
Biomind Labs Inc.
Start date
Dec 15, 2024
Tracker note / source boundary

ClinicalTrials.gov manual QA on 2026-04-17 | Status: Completed | Sponsor: Biomind Labs Inc. | Official title: A Phase 1/2 Randomized, Double-Blind, Placebo-Controlled Trial of Multiple Sublingual 5-MeO-DMT Microdoses for Reducing Anxiety and/or Depression in Patients With Mild Cognitive Impairment. | Condition: Mild Cognitive Impairment; Anxiety State; Depression Anxiety Disorder | Intervention: Sublingual 5-MeO-DMT microdoses plus psychiatric, cognitive, biochemical, and EEG assessments | Study type: Interventional

NCT06252506 Phase 1 Completed updated Mar 19, 2025

Molecular Imaging Study of Harmine/DMT: a Basic Research Approach

Condition
Neuropharmacological Investigation of Ayahuasca Constituents DMT and Harmine
Sponsor / institution
Insel Gruppe AG, University Hospital Bern
Start date
Jan 22, 2024
Tracker note / source boundary

ClinicalTrials.gov v2 sync on 2026-04-18 | Overall status: COMPLETED | Exact phase: Phase 1 | Lead sponsor: Insel Gruppe AG, University Hospital Bern | Conditions: Neuropharmacological Investigation of Ayahuasca Constituents DMT and Harmine | Interventions: N,N-dimethyltryptamine (DMT) + harmine; Placebo

NCT06816667 Phase 1/2 Completed updated Mar 5, 2025

Safety, Tolerability, and Efficacy of Sublingual Microdoses of 5-MeO-DMT for Depression and Anxiety (5-MeO-DMT)

Condition
Healthy Volunteers
Sponsor / institution
Biomind Labs Inc.
Start date
Oct 21, 2024
Tracker note / source boundary

ClinicalTrials.gov manual QA on 2026-04-17 | Status: Completed | Sponsor: Biomind Labs Inc. | Official title: A Phase 1/2 Randomized, Double-Blind, Placebo-Controlled Trial to Evaluate Safety, Tolerability and Efficacy of Multiple Sublingual Microdoses of 5-MeO-DMT in Reducing Symptoms of Depression and/or Anxiety. | Condition: Healthy Volunteers | Intervention: BMND08 sublingual 5-MeO-DMT formulation plus monitoring procedures | Study type: Interventional

NCT05839509 Phase 2 Stopped updated Feb 18, 2025

Phase 2 Clinical Trial of GH001 in Bipolar II Disorder

Condition
Bipolar II Disorder
Sponsor / institution
GH Research Ireland Limited
Start date
Apr 6, 2023
Tracker note / source boundary

ClinicalTrials.gov v2 sync on 2026-04-10 | Overall status: TERMINATED | Exact phase: Phase 2 | Lead sponsor: GH Research Ireland Limited | Conditions: Bipolar II Disorder

NCT05804708 Phase 2 Stopped updated Feb 18, 2025

Phase 2 Clinical Trial of GH001 in Postpartum Depression

Condition
Postpartum Depression, Postnatal Depression
Sponsor / institution
GH Research Ireland Limited
Start date
Mar 2, 2023
Tracker note / source boundary

ClinicalTrials.gov v2 sync on 2026-04-10 | Overall status: TERMINATED | Exact phase: Phase 2 | Lead sponsor: GH Research Ireland Limited | Conditions: Postpartum Depression; Postnatal Depression

NCT05559931 Phase 1 Active updated Jan 28, 2025

Single and Repeat Doses of DMT in Healthy Subjects

Condition
Stroke
Sponsor / institution
Algernon Pharmaceuticals
Start date
Jan 13, 2023
Tracker note / source boundary

ClinicalTrials.gov v2 sync on 2026-04-18 | Overall status: ACTIVE_NOT_RECRUITING | Exact phase: PHASE1 | Lead sponsor: Algernon Pharmaceuticals | Conditions: Stroke | Interventions: N,N-Dimethyltryptamine; Placebo | Notes: Tracker status mapped to Active because ACTIVE_NOT_RECRUITING is not an available status option.

NCT06094907 Phase 2 Completed updated May 8, 2024

Safety, Tolerability and Antidepressant Effects of DMT in Patients With Depression

Condition
Depressive Disorder, Depression, Unipolar
Sponsor / institution
Universidade Federal do Rio Grande do Norte
Start date
Oct 9, 2023
Tracker note / source boundary

ClinicalTrials.gov v2 sync on 2026-04-18 | Overall status: COMPLETED | Exact phase: PHASE2 | Lead sponsor: Universidade Federal do Rio Grande do Norte | Conditions: Depressive Disorder; Depression, Unipolar | Interventions: N,N-Dimethyltryptamine

NCT05384678 Phase 1 Completed updated Apr 25, 2024

Acute Dose-dependent Effects of DMT in Healthy Subjects (DMT DR)

Condition
Healthy
Sponsor / institution
University Hospital, Basel, Switzerland
Start date
Nov 15, 2022
Tracker note / source boundary

ClinicalTrials.gov manual QA on 2026-04-17 | Status: Completed | Sponsor: University Hospital, Basel, Switzerland | Official title: Acute Dose-dependent Effects of DMT in Healthy Subjects: A Placebo-controlled Cross-over Study | Condition: Healthy | Intervention: N,N-Dimethyltryptamine dose-ranging arms plus placebo | Study type: Interventional

NCT05698095 Phase 1 Completed updated Nov 30, 2023

Pharmacokinetics, Safety, and Tolerability of Intramuscular 5-MeO-DMT in Healthy Volunteers

Condition
Pharmacokinetics; Safety; Tolerability
Sponsor / institution
Usona Institute
Start date
Dec 27, 2022
Tracker note / source boundary

ClinicalTrials.gov manual QA on 2026-04-17 | Status: Completed | Sponsor: Usona Institute | Official title: A Phase 1, First-in-human, Double-blind, Placebo-controlled, Randomized, Single- and Multiple-ascending-dose Study to Determine the Safety, Tolerability, and Pharmacokinetics of 5-methoxy-N,N-dimethyltryptamine (5-MeO-DMT) Administered by Intramuscular Injection in Healthy Subjects | Condition: Pharmacokinetics; Safety; Tolerability | Intervention: 5-methoxy-N,N-dimethyltryptamine succinate salt; Placebo | Study type: Interventional

NCT05829603 Phase 1 Completed updated Nov 2, 2023

Dose-finding Study for the Combination of DMT and Harmine in Healthy Subjects

Condition
Healthy
Sponsor / institution
Reconnect Labs
Start date
May 5, 2023
Tracker note / source boundary

ClinicalTrials.gov v2 sync on 2026-04-18 | Overall status: COMPLETED | Exact phase: PHASE1 | Lead sponsor: Reconnect Labs | Conditions: Healthy | Interventions: Dimethyltryptamin (DMT) & Harmine | Notes: DMT + harmine combination tagged as Ayahuasca, DMT because the registry explicitly lists both ayahuasca-relevant constituents.

NCT05901012 Phase 1 Completed updated Oct 11, 2023

Safety and Tolerability of DMT in Healthy Adults

Condition
Safety Issues, Healthy Volunteers
Sponsor / institution
Universidade Federal do Rio Grande do Norte
Start date
Apr 26, 2023
Tracker note / source boundary

ClinicalTrials.gov v2 sync on 2026-04-18 | Overall status: COMPLETED | Exact phase: PHASE1 | Lead sponsor: Universidade Federal do Rio Grande do Norte | Conditions: Safety Issues; Healthy Volunteers | Interventions: N,N-Dimethyltryptamine; Placebo

NCT05780216 Phase 1 Completed updated Sep 21, 2023

Mindfulness and Psychedelics

Condition
Healthy Participants
Sponsor / institution
Milan Scheidegger
Start date
Feb 20, 2023
Tracker note / source boundary

ClinicalTrials.gov v2 sync on 2026-04-18 | Overall status: COMPLETED | Exact phase: Early Phase 1 | Lead sponsor: Milan Scheidegger | Conditions: Healthy Participants | Interventions: DMT + harmine; Placebo | Notes: Summary explicitly frames Ayahuasca as the relevant plant preparation context.

NCT04640831 Phase 1 Completed updated Aug 15, 2023

Safety of GH001 in Healthy Volunteers

Condition
Healthy Volunteers
Sponsor / institution
GH Research Ireland Limited
Start date
Mar 13, 2019
Tracker note / source boundary

ClinicalTrials.gov v2 sync on 2026-04-10 | Overall status: COMPLETED | Exact phase: Phase 1 | Lead sponsor: GH Research Ireland Limited | Conditions: Healthy Volunteers

NCT04698603 Phase 1 Completed updated Aug 15, 2023

Clinical Study of GH001 in Depression

Condition
Treatment Resistant Depression, Major Depressive Disorder, Depression
Sponsor / institution
GH Research Ireland Limited
Start date
Nov 12, 2019
Tracker note / source boundary

ClinicalTrials.gov v2 sync on 2026-04-10 | Overall status: COMPLETED | Exact phase: Phase 1, Phase 2 | Lead sponsor: GH Research Ireland Limited | Conditions: Treatment Resistant Depression; Major Depressive Disorder; Depression

NCT05032833 Phase 1 Completed updated Oct 12, 2022

Single Ascending Dose Study With 5-MeO-DMT in Healthy Subjects

Condition
Pharmacokinetics in Healthy Adults
Sponsor / institution
Beckley Psytech Limited
Start date
Sep 22, 2021
Tracker note / source boundary

ClinicalTrials.gov manual QA on 2026-04-17 | Status: Completed | Sponsor: Beckley Psytech Limited | Official title: A Double-Blind, Randomized, Phase 1, First-in-Human, Single Ascending Dose Study to Evaluate the Safety, Tolerability and Pharmacokinetic Profile of Intranasal 5-Methoxy-N,N-dimethyltryptamine (5-MeO-DMT) in Healthy Subjects | Condition: Pharmacokinetics in Healthy Adults | Intervention: 5-MeO-DMT; Placebo | Study type: Interventional

NCT04353024 Phase 1 Completed updated Oct 12, 2022

Effects of Dimethyltryptamine in Healthy Subjects (DMT)

Condition
Healthy
Sponsor / institution
University Hospital, Basel, Switzerland
Start date
Jun 18, 2021
Tracker note / source boundary

ClinicalTrials.gov manual QA on 2026-04-17 | Status: Completed | Sponsor: University Hospital, Basel, Switzerland | Official title: Effects of Dimethyltryptamine (DMT) in Healthy Subjects: A Placebo-controlled Cross-over Study | Condition: Healthy | Intervention: Dimethyltryptamine (DMT); Saline | Study type: Interventional

NCT04716335 Phase 1 Completed updated Oct 4, 2022

Neurodynamics of Prosocial Emotional Processing Following Serotonergic Stimulation With N,N-Dimethyltryptamine (DMT) and Harmine in Healthy Subjects

Condition
Emotions, Mood, Cognitive Function 1, Social, Empathy
Sponsor / institution
Psychiatric University Hospital, Zurich
Start date
Dec 1, 2020
Tracker note / source boundary

ClinicalTrials.gov v2 sync on 2026-04-18 | Overall status: COMPLETED | Exact phase: EARLY_PHASE1 | Lead sponsor: Psychiatric University Hospital, Zurich | Conditions: Emotions; Mood; Cognitive Function 1, Social; Empathy | Interventions: DMT; Harmine; Placebo (Harmine); Placebo (DMT) | Notes: DMT + harmine combination tagged as Ayahuasca, DMT because the registry explicitly lists both ayahuasca-relevant constituents.

NCT05163691 Phase 1 Completed updated Dec 20, 2021

Pharmacokinetics of GH001 in Healthy Volunteers

Condition
Healthy Volunteers
Sponsor / institution
GH Research Ireland Limited
Start date
Jun 21, 2021
Tracker note / source boundary

ClinicalTrials.gov v2 sync on 2026-04-10 | Overall status: COMPLETED | Exact phase: Phase 1 | Lead sponsor: GH Research Ireland Limited | Conditions: Healthy Volunteers

May 15, 2026 Last checked 2026-05-15 UTC Publication Research

Neuropharmacology reports DMT not formed or retained in rat serotonin terminals

Claim boundary.preclinical/basic-neurochemistry rat-brain study only; useful for tightening endogenous-DMT claim boundaries, not for adjudicating human psychedelic experience, clinical efficacy/safety, approval, label, reimbursement, or access.

PubMed PMID 41672133 / Neuropharmacology tested endogenous and exogenous DMT handling in rat brain after monoamine-oxidase, acidic-metabolite-transport, serotonin-uptake, and vesicular-monoamine-transporter manipulations. The authors report no evidence that DMT is formed or stored in serotonin terminals and emphasize rapid metabolism of exogenous DMT.

Source/tracker note

Last checked 2026-05-15 UTC. Claim boundary: preclinical/basic-neurochemistry rat-brain study only; useful for tightening endogenous-DMT claim boundaries, not for adjudicating human psychedelic experience, clinical efficacy/safety, approval, label, reimbursement, or access.

May 12, 2026 Last checked 2026-05-16 UTC Trial Update Company

AtaiBeckley Q1 2026 update: BPL-003 Phase 3 design, VLS-01 timing, EMP-01 R-MDMA SAD signal

Claim boundary.company-reported pipeline/capitalization and Phase 3-design tracker only; not approval, label, reimbursement, access, independent efficacy/safety confirmation, or proof that planned Phase 3 studies will start/succeed. Keep BPL-003, VLS-01, and EMP-01 separate from unrelated CNPV/company-primary-pending items.

AtaiBeckley company release says BPL-003 Phase 3 ReConnection remains on track for Q2 2026, with ReConnection-1 ~350 and ReConnection-2 ~230, MADRS Week 4 primary, and 52-week OLE; VLS-01 Phase 2 Elumina topline is anticipated Q4 2026; EMP-01 oral R-MDMA Phase 2a in SAD showed company-described convergent improvements; cash/securities were $209.9M with runway into 2029.

Source/tracker note

Last checked 2026-05-16 UTC. Claim boundary: company-reported pipeline/capitalization and Phase 3-design tracker only; not approval, label, reimbursement, access, independent efficacy/safety confirmation, or proof that planned Phase 3 studies will start/succeed. Keep BPL-003, VLS-01, and EMP-01 separate from unrelated CNPV/company-primary-pending items.

May 8, 2026 Last checked 2026-05-15 UTC Publication Research

Clinical Pharmacology & Therapeutics maps registered ayahuasca/DMT trials

Claim boundary.review/registry-map item only; supports wiki/trial-landscape context, not clinical efficacy/safety conclusion, approval, label, reimbursement, or access.

PubMed PMID 42104189 / Clinical Pharmacology & Therapeutics scoping review identifies 26 eligible registered interventional trials of DMT, ayahuasca, and DMT plus harmine on ClinicalTrials.gov. Review says the registry landscape expanded after 2020–2021 and remains dominated by early-stage safety/physiological and subjective-effect characterization, with disorder-specific symptom endpoints less often primary.

Source/tracker note

Last checked 2026-05-15 UTC. Claim boundary: review/registry-map item only; supports wiki/trial-landscape context, not clinical efficacy/safety conclusion, approval, label, reimbursement, or access.

Mar 5, 2026 Last checked 2026-05-16 UTC Trial Update Company

Helus HLP004/CYB004 Phase 2 GAD topline company release backfill

Claim boundary.company-reported topline/backfill only; not peer-reviewed publication, approval, label, reimbursement, access, independent efficacy confirmation, broad safety, or Phase 3 success. Company reports no drug-related SAEs/suicidality-related signals and acute effects ~90 min, but these remain company topline claims from a small signal-detection study.

Helus/Cybin company release reports topline Phase 2 signal-detection results for HLP004 in GAD: 36 patients randomized 2:1 active-to-control, two intramuscular doses three weeks apart, company-reported HAM-A change and six-month response/remission summaries; registry cross-check is NCT06051721.

Source/tracker note

Last checked 2026-05-16 UTC. Claim boundary: company-reported topline/backfill only; not peer-reviewed publication, approval, label, reimbursement, access, independent efficacy confirmation, broad safety, or Phase 3 success. Company reports no drug-related SAEs/suicidality-related signals and acute effects ~90 min, but these remain company topline claims from a small signal-detection study.

Bipolar II DisorderDepressive Disorder, Depression, UnipolarEmotions, Mood, Cognitive Function 1, Social, EmpathyGeneralized Anxiety DisorderHealthyHealthy AdultHealthy ParticipantsHealthy VolunteersMajor Depressive Disorder, Psychedelic ExperiencesMild Cognitive Impairment; Anxiety State; Depression Anxiety DisorderNeuropharmacological Investigation of Ayahuasca Constituents DMT and HarminePharmacokinetics in Healthy AdultsPharmacokinetics; Safety; TolerabilityPostpartum Depression, Postnatal DepressionPTSD - Post Traumatic Stress Disorder; Cognitive Dysfunction; Brain Trauma; Brain InjuriesSafety Issues, Healthy VolunteersStrokeTreatment Resistant DepressionTreatment Resistant Depression, Major Depressive Disorder, DepressionTreatment-resistant Depression