Forecast Ledgerinterventional psychiatry and psychedelic medicineQuoted, dated predictions scored against public outcomes under one written method. Every score links to the words, the rule and the evidence.

Known true · enters 1 Jul 2027

Rules 1.1.0 · as of 14 Sep 2026

Quote

“Furthermore, BPL-003 might deliver even stronger results with a 2-dose induction, to be proven with further data.”
· atai Life Sciences – Strong Phase 2b topline data for BPL-003 (5-MeO-DMT) and further strategic backing · own post

Section 'The Two-Hour Window: Our Sweet Spot'.

Intake

EventA proposition written from a template on the asset, with a resolution criterion and a named public source, before the outcome is looked up. The same event resolves every person's items on it. Method ›
BPL-003 two-dose induction reports a larger antidepressant effect than the single-dose Phase 2b result
AreaOne of five topic classes: regulatory decisions, clinical trial outcomes, company and market outcomes, payer and policy, practice adoption. Every event has one area. Method ›
Trial outcomes
DeadlineThe date by which the event must happen for the item to be true. It comes only from the person's words through the anchor table. Method ›
None stated · undated panelItems with no deadline in the person's words, scored on a uniform 24-month window from the statement date. Part of the headline panel since rules 1.1.0; also shown on its own. Method ›, 24-month window to 1 Jul 2027
Probability
0.50 LexiconThe fixed five-bin table that turns a phrase into a probability. The strongest phrase in the claim sentence decides; coders never read tone. Method › · binOne of five lexicon steps: A 'will' 0.90, B 'probably' 0.70, C 'may' 0.50, D 'unlikely' 0.30, E 'never' 0.10. A stated number goes to the nearest bin for calibration only. Method › C · “might deliver even stronger results”
Base rateThe probability a published external study gives an event of that class and stage, fixed at intake. Halved when the item window is shorter than the class median time to decision. Never learned from the ledger's own items. Method ›
None in the table
Tags
affiliated, retrospective
Coder BCohen's kappa: agreement between two coders beyond chance, from -1 to 1. Reported for admit, event, deadline, bin and asserts from the second-coder match test. Method ›
admittedA statement that passed intake: sincere, the person's own claim, forward-looking, inside the five areas, and not excluded by a reason code. Only admitted statements become items. Method › · event E-0106 · deadline none · bin C
Registry entry

The sponsor reports data in which a two-dose induction regimen of BPL-003 produces a larger reduction in depression score (MADRS) than the single-dose Phase 2b result.

TRUE on the date of the first sponsor topline press release, ClinicalTrials.gov results posting or peer-reviewed publication that reports a two-dose induction regimen of BPL-003 (intranasal 5-MeO-DMT) in treatment-resistant depression with a larger point-estimate reduction from baseline in the MADRS total score, at the primary timepoint, than the estimate the sponsor reported for the corresponding single active dose in the BPL-003 Phase 2b trial the forecaster describes. The comparison is on the reported point estimates; statistical significance of the difference is not required. FALSE on the date the sponsor first reports a two-dose induction estimate that is not larger, and FALSE at the deadline when no two-dose induction data have been reported.

Resolution source: Sponsor topline press release; ClinicalTrials.gov results or peer-reviewed publication as a secondary source

Readings: 'Even stronger results' is read as a larger reduction in the MADRS total score, the primary depression measure of the Phase 2b trial the forecaster summarises in the same post.; 'To be proven with further data' names the resolution event: the sponsor must report two-dose induction data, not merely plan them.; 'Might deliver' is a hedge on likelihood, not a condition.

How to read
The event, criterion and deadline were written at intake, before the outcome1 if the registry event happened on or before the item's deadline, 0 if it did not. Written by a resolver who never sees p. Method › was looked up. Coder B coded the statement independently.

Coder A

Resolution

State
Known trueAn item whose event has already happened but whose deadline has not passed. Shown as 'known true, enters on <deadline>'; pending in every metric until then. Method ›
Effective deadlineAn item enters the score only when its deadline has passed and the outcome is true or false. A claim already known true still waits for its deadline. Method ›
1 Jul 2027
Outcome1 if the registry event happened on or before the item's deadline, 0 if it did not. Written by a resolver who never sees p. Method ›
occurred on 23 Sep 2025 · checked through 14 Sep 2026
Resolver note
On 2025-09-23 the sponsor reported the Phase 2a two-dose induction regimen (NCT05660642, 8 mg then 12 mg two weeks later, n=13 enrolled, 12 per protocol): mean MADRS reduction from baseline 13.3 points at day 2, 12.9 at day 8, 19.0 one week after the second dose, and 13.7 at week 12. The corresponding single active dose in the Phase 2b (2025-07-01) gave 12.1 points for 8 mg and 11.1 for 12 mg at the day 29 primary timepoint. The two-dose point estimate, 19.0, is larger, and the week 12 estimate, 13.7, is also larger. The 2025-11-10 Phase 2b open-label extension confirms the direction: 22.3 points at day 57 for patients whose first dose was 8 mg. The criterion asks only for a larger point estimate, not a significant difference.
BrierThe squared gap between a probability and the outcome, (p - o)^2. 0 is perfect, 0.25 is the constant coin flip, 1 is confidently wrong. Lower is better. Method ›
Not scored
Adversarial recheck

upheld (state): Argued not_occurred on the criterion words 'at the primary timepoint'. The Phase 2b primary timepoint is Day 29; the 2025-09-23 Phase 2a two-dose release reports Day 2, Day 8, one week after the second dose and Week 12, but no Day 29 value, so a strict same-timepoint comparison has no matching number. The argument fails on the size of the gap. Phase 2b single active doses: 12.1 points (8 mg) and 11.1 points (12 mg) at Day 29. Phase 2a two-dose induction (8 mg then 12 mg): 19.0 points one week after the second dose and 13.7 points at Week 12, both larger than either single-dose estimate; even the pre-second-dose Day 8 value, 12.9, exceeds them. The criterion asks only for a larger point estimate, not significance and not a matched day. No earlier two-dose induction report exists. Upheld.

How to read
State at window close; the outcome comes from the registry, the score from the rule.

Registry

Receding horizon

Angermayer promised BPL-003 two-dose induction reports a larger antidepressant effect than the single-dose Phase 2b result 2 times; it happened on 23 Sep 2025.

promised datehappened
202620272028202620272028TODAY2025-07-01: by 2027-07-01 · p 0.502026-02-18: by 2028-02-18 · p 0.50HAPPENED 2025-09-23X SAID ON · Y PROMISED BY · DASHED: PROMISED = SAID · DOT AREA = P

Cluster E-0106

Timeline

1 claim against 15 events in the field.

saiddueevent
1 Jul 2025 · atai Life Sciences / Beckley Psytech (BPL-003): Phase 2b of single-dose intranasal BPL-003 (5-MeO-DMT) in TRD meets primary and 4 Sep 2025 · MindMed (MM120): JAMA publishes MindMed's phase 2b of MM120 in GAD, the first placebo-controlled 22 Sep 2025 · Johnson & Johnson (seltorexant, MDD3005): Phase 3 MDD3005 misses its primary endpoint: seltorexant showed only numerically3 Dec 2025 · Bristol Myers Squibb (Cobenfy, ADEPT-2): BMS delays the ADEPT-2 phase 3 readout in Alzheimer's disease psychosis to end-2BRISTOL MYERS SQUIBB (COBENFY, ADEPT-2): BMS DELAYS THE ADEPT-2 PHASE 3 READOUT IN ALZHEIMER'S DISEASE PSYCHOSIS TO END-217 Feb 2026 · Compass Pathways (COMP360, COMP006): Second phase 3 COMP006 meets primary endpoint: two 25 mg COMP360 doses 3 weeks a5 Mar 2026 · Helus Pharma (HLP004 / CYB004, GAD): Helus reports phase 2 signal-detection results for deuterated DMT HLP004 in mode1 Apr 2026 · Alto Neuroscience (ALTO-101): Alto's phase 2 proof-of-concept of ALTO-101 in cognitive impairment associated w8 Apr 2026 · AtaiBeckley (BPL-003): AtaiBeckley publishes phase 2a data of BPL-003 in TRD patients on SSRIs (CNS Dru26 May 2026 · US Department of Veterans Affairs: VA launches its MDMA-assisted therapy trial for veterans with PTSD and alcohol u15 Jun 2026 · Neumora Therapeutics (navacaprant, KOASTAL-2/3): KOASTAL-2 and KOASTAL-3 both miss; Neumora discontinues navacaprant after three 22 Jun 2026 · Definium Therapeutics (DT120 / MM120, Emerge): Phase 3 Emerge of single-dose DT120 (LSD) ODT 100 µg in MDD meets its primary en7 Jul 2026 · Compass Pathways (COMP360, COMP006): COMP006 26-week (Part B) data show benefit of two 25 mg doses maintained on aver21 Jul 2026 · Helus Pharma (HLP003 / CYB003, APPROACH): Helus completes enrollment in the phase 3 APPROACH study of HLP003 as adjunctive12 Aug 2026 · Definium Therapeutics (DT120 / MM120, Voyage): Phase 3 Voyage of DT120 ODT 100 µg in GAD meets its primary HAM-A endpoint at we9 Sep 2026 · Compass Pathways (COMP360, COMP005 Part C): Compass reports 52-week open-label COMP005 data: participants who received an adBPL-003 TWO-DOSE…BPL-003 two-dose induction reports a larger antidepressant effect than the single-dose Phase 2b result · stated 1 Jul 2025BPL-003 two-dose induction reports a larger antidepressant effect than the single-dose Phase 2b result · restated 1 Jul 2025 · p 50%50%TODAY20262027

Trial outcomes