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