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.

False · Brier 0.09

Rules 1.1.0 · as of 14 Sep 2026

Quote

“There are many reasons a trial will fail, and the ar ketamine story is unlikely to be over yet.”
· Spravato · substack post

After quoting atai Life Sciences' announcement that PCN-101 (R-ketamine, arketamine, Perception Neuroscience) missed its Phase 2a primary endpoint at 24 hours, the author expects the arketamine development story to continue.

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 ›
PCN-101 (arketamine) development is discontinued
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 29 Mar 2026
Probability
0.30 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 › D · “unlikely to be over yet”
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
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-0021 · deadline none · bin D
Registry entry

The sponsor of PCN-101 (arketamine) announces that clinical development of the program is discontinued.

TRUE on the date of the first definitive public statement by the sponsor of PCN-101 (atai Life Sciences, its subsidiary Perception Neuroscience, or a successor owner or licensee of the asset), in a press release, SEC filing or investor presentation, that development of PCN-101 (arketamine, R-ketamine) is discontinued or terminated, or that the program has been removed from the pipeline with no further development planned. A missed endpoint, a pause pending data, a search for a partner, or a deprioritization that keeps the program under evaluation is not discontinuation. Development that continues under a licensee or new owner of the asset is not discontinuation. Resolution source: atai Life Sciences press releases and SEC filings (EDGAR). FALSE at the deadline when no such discontinuation statement has been made.

Resolution source: atai Life Sciences press releases and SEC filings (EDGAR)

Readings: 'The arketamine story is over' is read as the sponsor discontinuing the PCN-101 (arketamine) program, the only arketamine program in the post. The forecaster says this is unlikely.; The event is written on the asset, so it follows PCN-101 through a rename, a partnership or a sale; continued development by a licensee or new owner keeps the event FALSE.

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
False
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 ›
29 Mar 2026
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 ›
not occurred · checked through 13 Sep 2026
Resolver note
No sponsor statement of discontinuation was found; all 15 EDGAR full-text hits for PCN-101/arketamine since 2024 were reviewed. The FY2024 10-K (2025-03-17) says atai is 'seeking strategic partnership options, for example, with ... Perception Neuroscience' and reports Otsuka's January 2025 notice terminating its Japan arketamine license effective 2025-04-24 (a licensee action, not sponsor discontinuation). The FY2025 10-K (2026-03-06) and Q2 2026 10-Q (2026-08-11) still report direct R&D expenses for PCN-101 and Perception Neuroscience as a 59.2%-owned controlled VIE; PCN-101 is absent from the pipeline text, but no filing or release says development is discontinued or removed with no further development planned. A partner search or deprioritization is not discontinuation under the criterion. Wikipedia's 'previous candidate' label has no sponsor source. Not occurred as of 2026-09-13.
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 ›
0.09 = (0.30 − 0)²
How to read
State at window close; the outcome comes from the registry, the score from the rule.

Registry

Timeline

1 claim against 29 events in the field.

saiddueevent
30 May 2024 · Johnson & Johnson (seltorexant, MDD3001): J&J reports phase 3 MDD3001: adjunctive seltorexant met all primary and secondarJOHNSON & JOHNSON (SELTOREXANT, MDD3001): J&J REPORTS PHASE 3 MDD3001: ADJUNCTIVE SELTOREXANT MET ALL PRIMARY AND SECONDAR11 Aug 2024 · MAPS / Lykos (Psychopharmacology): Psychopharmacology retracts three MDMA-assisted therapy papers by MAPS/Lykos aut22 Oct 2024 · Alto Neuroscience (ALTO-100): Alto's biomarker-selected phase 2b of ALTO-100 in MDD misses its primary MADRS e11 Nov 2024 · AbbVie (emraclidine, EMPOWER-1/2): AbbVie's muscarinic agonist emraclidine, acquired via the $8.7B Cerevel deal, fa18 Nov 2024 · Cybin (CYB003): Cybin reports 12-month phase 2 follow-up for CYB003 in MDD with sustained respon3 Dec 2024 · US Department of Veterans Affairs: VA announces funding for its first study of MDMA-assisted therapy in decades, fo9 Dec 2024 · Relmada Therapeutics (REL-1017): Relmada halts its two remaining phase 3 trials of esmethadone after a futility s2 Jan 2025 · Neumora Therapeutics (navacaprant, KOASTAL-1): Neumora's phase 3 KOASTAL-1 of kappa-opioid antagonist navacaprant in MDD misses3 Feb 2025 · GH Research (GH001): GH Research reports its phase 2b of inhaled mebufotenin (5-MeO-DMT) GH001 in TRD12 Feb 2025 · Alto Neuroscience (ALTO-300): Alto reports a favorable interim analysis of its EEG-biomarker phase 2b of adjun3 Mar 2025 · Neumora Therapeutics (navacaprant): Neumora halts one navacaprant depression trial and redesigns the KOASTAL-2 and K6 Mar 2025 · Johnson & Johnson (aticaprant, VENTURA): J&J stops the phase 3 VENTURA program of kappa-opioid antagonist aticaprant in M22 Apr 2025 · Bristol Myers Squibb (Cobenfy, ARISE): Phase 3 ARISE misses: adjunctive Cobenfy did not significantly beat placebo on P23 Jun 2025 · Compass Pathways (COMP360, COMP005): Compass reports phase 3 COMP005 met its primary endpoint: a single 25 mg COMP3601 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-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 adPCN-101 (ARKETAMI…PCN-101 (arketamine) development is discontinued · stated 29 Mar 2024PCN-101 (arketamine) development is discontinued · restated 29 Mar 2024 · p 30%PCN-101 (arketamine) development is discontinued · miss 29 Mar 202630%TODAY20252026

Trial outcomes