Clinical-stage developers of psilocybin, MDMA, and next-generation psychedelic compounds.
Ticker
Company
Last
Change
%
Compass Pathways
11.53
−0.47
−3.92%
CMPSCompass PathwaysNasdaq · USDPsychedelics
$11.53−3.92%Oct 12, 2026, 4:00 PM ET · delayed
Open
$12.02
Day high
$12.05
Day low
$11.53
Volume
1.95M
Mkt cap
$1.60B
52w range
$4.88–$15.87
Price · last 1M
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Pipeline
CompoundIndicationAgencyPhase
COMP360 psilocybin
Treatment-resistant depression
FDA
Ph. 3
Status Phase 3 complete; rolling NDA underway
Latest milestone · Aug 5, 2026 Rolling NDA submission and initial review underway; final submission expected to be completed in Q4 (Compass Pathways Q2 2026 results press release (Form 8-K, Exhibit 99.1))
Status Breakthrough designation; Phase 3 APPROACH enrollment completed July 2026, topline expected Q4 2026
Latest milestone · Jul 21, 2026 Enrollment completed in the Phase 3 APPROACH study (223 participants); topline data readout targeted for Q4 2026 (Helus Pharma press release (Form 6-K, Exhibit 99.1))
HLP004 (deuterated DMT)
Generalized anxiety disorder
FDA
Ph. 2
Status Phase 2 signal-detection topline reported March 2026 (adjunct to standard of care)
Latest milestone · Mar 5, 2026 Topline results announced from the Phase 2 HLP004-002 study in generalized anxiety disorder (Helus Pharma MD&A for the quarter ended 2026-06-30 (Form 6-K, Exhibit 99.2))
Profile facts come from the company's SEC filings; hover a value for its source and date. Quotes are delayed.
GH Research
20.02
−1.09
−5.16%
GHRSGH ResearchNasdaq · USDPsychedelics
$20.02−5.16%Oct 12, 2026, 4:00 PM ET · delayed
Open
$21.06
Day high
$21.23
Day low
$20.01
Volume
229.7K
Mkt cap
$1.37B
52w range
$12.04–$31.44
Price · last 1M
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Pipeline
CompoundIndicationAgencyPhase
GH001 (inhaled mebufotenin)
Treatment-resistant depression
FDA
Ph. 2
Status Phase 2b positive; FDA written responses confirm CMC and device plans appear Phase 3 ready; pivotal program initiation targeted in 2026
Latest milestone · Aug 6, 2026 FDA written responses (received July 2026) confirmed CMC and device plans appear Phase 3 ready; initiation of the pivotal program targeted in 2026 (GH Research second-quarter 2026 results press release (Form 6-K, Exhibit 99.3))
Profile facts come from the company's SEC filings; hover a value for its source and date. Quotes are delayed.
Axsome Therapeutics
166.00
−2.35
−1.40%
AXSMAxsome TherapeuticsNasdaq · USDPharma
$166.00−1.40%Oct 12, 2026, 4:00 PM ET · delayed
Open
$169.41
Day high
$170.80
Day low
$165.02
Volume
663.0K
Mkt cap
$8.70B
52w range
$119.20–$260.19
Price · last 1M
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Tracked mental-health programs
CompoundIndicationAgencyPhase
AXS-05 (Auvelity)
Major depressive disorder
FDA
Approved
Status Marketed
AXS-05 (Auvelity)
Agitation associated with dementia due to Alzheimer's disease
FDA
Approved
Status FDA approved April 2026
Latest milestone · Apr 30, 2026 FDA approved AUVELITY for the treatment of agitation associated with dementia due to Alzheimer's disease (Axsome Therapeutics press release (Form 8-K, Exhibit 99.1))
Profile facts come from the company's SEC filings; hover a value for its source and date. Quotes are delayed.
Acadia Pharmaceuticals
19.41
−0.37
−1.87%
ACADAcadia PharmaceuticalsNasdaq · USDPharma
$19.41−1.87%Oct 12, 2026, 4:00 PM ET · delayed
Open
$19.70
Day high
$19.87
Day low
$19.40
Volume
1.18M
Mkt cap
$3.34B
52w range
$19.32–$30.96
Price · last 1M
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Tracked mental-health programs
CompoundIndicationAgencyPhase
Remlifanserin (formerly ACP-204)
Alzheimer's disease psychosis
FDA
Ph. 3
Status Phase 2 portion of RADIANT narrowly missed its primary endpoint (p=0.0603); company plans to continue its two ongoing Phase 3 studies in ADP, without the 30 mg arm; FDA Fast Track granted July 2026; Phase 2 in Lewy body dementia psychosis ongoing
Latest milestone · Sep 24, 2026 Phase 2 RADIANT topline: primary endpoint narrowly missed (SAPS-H+D p=0.0603); company plans to continue enrolling its two ongoing Phase 3 studies and remove the 30 mg arm (Acadia Pharmaceuticals press release (Form 8-K, Exhibit 99.1))
Profile facts come from the company's SEC filings; hover a value for its source and date. Quotes are delayed.
Eli Lilly
1182.62
+3.35
+0.28%
LLYEli LillyNYSE · USDPharma
$1182.62+0.28%Oct 12, 2026, 4:00 PM ET · delayed
Open
$1181.24
Day high
$1188.58
Day low
$1172.81
Volume
1.25M
Mkt cap
$1.05T
52w range
$783.85–$1292.65
Price · last 1M
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Tracked mental-health programs
CompoundIndicationAgencyPhase
Brenipatide (LY3537031)
Major depressive disorder; alcohol use disorder
Ph. 3
Status Phase 3 recruiting in MDD and alcohol use disorder; Phase 2 in bipolar disorder and schizophrenia
BPL-003 (intranasal mebufotenin)
Treatment-resistant depression
FDA
Ph. 3
Status Phase 3 initiated; Lilly acquisition closed Sept 11, 2026
Latest milestone · Sep 11, 2026 Lilly completed its acquisition of AtaiBeckley, whose lead program BPL-003 (FDA Breakthrough Therapy designation) has initiated Phase 3 activities (AtaiBeckley Form 8-K (Items 2.01, 3.01, 3.03, 5.01, 5.02, 5.03 and 9.01))
VLS-01 (buccal DMT)
Treatment-resistant depression
Ph. 2
Status Phase 2b Elumina study in TRD: last patient dosed; topline results anticipated Q4 2026
Latest milestone · Aug 11, 2026 Phase 2b Elumina study in TRD: last patient dosed; topline results anticipated in Q4 2026 (AtaiBeckley Form 10-Q for the quarter ended 2026-06-30)
Profile facts come from the company's SEC filings; hover a value for its source and date. Quotes are delayed.
Johnson & Johnson
263.73
+2.29
+0.88%
JNJJohnson & JohnsonNYSE · USDPharma
$263.73+0.88%Oct 12, 2026, 4:00 PM ET · delayed
Open
$261.60
Day high
$264.39
Day low
$260.37
Volume
5.64M
Mkt cap
$635.56B
52w range
$184.66–$281.07
Price · last 1M
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Tracked mental-health programs
CompoundIndicationAgencyPhase
Esketamine (Spravato)
Treatment-resistant depression
FDA
Approved
Status FDA approved as monotherapy for adults with treatment-resistant depression (January 2025)
Latest milestone · Jan 21, 2025 FDA approved SPRAVATO as the first and only monotherapy for adults with treatment-resistant depression (Johnson & Johnson press release, January 21, 2025)
Seltorexant
Major depressive disorder with insomnia symptoms
Ph. 3
Status MDD3001 positive; MDD3005 vs quetiapine XR missed primary endpoint (Sept 2025); additional Phase 3 recruiting
Latest milestone · Sep 22, 2025 Phase 3 MDD3005 against quetiapine XR: numerically greater 26-week response (57.4% vs 53.4%), primary endpoint not met (Johnson & Johnson press release, September 22, 2025)
Profile facts come from the company's SEC filings; hover a value for its source and date. Quotes are delayed.
AbbVie
281.12
+4.65
+1.68%
ABBVAbbVieNYSE · USDPharma
$281.12+1.68%Oct 12, 2026, 4:03 PM ET · delayed
Open
$277.65
Day high
$281.27
Day low
$276.01
Volume
5.49M
Mkt cap
$496.77B
52w range
$190.75–$281.27
Price · last 1M
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Tracked mental-health programs
CompoundIndicationAgencyPhase
Emraclidine
Schizophrenia
Ph. 2
Status Phase 2 EMPOWER trials missed their primary endpoint; AbbVie recorded a $4.5B impairment. A separate Phase 2 schizophrenia study remains ongoing.