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CMPS US Equity

COMPASS Pathways plcHealth Care · Pharmaceutical Preparations · CIK 1816590 · FY ends Dec 31
$13.90
+0.18 (+1.31%)
USD · as of 2026-08-18 · marketstack
9 registered studies · 3 active

Studies where CMPS is the lead sponsor, as filed with ClinicalTrials.gov. Completion dates are the sponsor's own projected windows and are revised as a study runs. Active studies first, then completed and stopped — newest readout first within each.

8 interventional · 1 observational · 3 with posted results

Held by 15 tracked-famous managers (TWO SIGMA INVESTMENTS, LP, MARSHALL WACE, LLP, Point72 Asset Management, L.P., RENAISSANCE TECHNOLOGIES LLC, CITADEL ADVISORS LLC, +10 more) · FINRA short interest 3.6 days to cover (settled 2026-07-31) · government filings 180d: none disclosed

StudyPhaseStatusInterventionsConditionsEnrollmentPrimary completionReadout inUpdated
Redefine Study: A Study Evaluating the Efficacy, Safety, and Tolerability of COMP360 in Participants With Post-traumatic Stress DisorderNCT07570654COMP360 25 mg versus COMP360 1 mg change from Baseline to Week 8 in CAPS-5 total severity scoreRandomized · Quadruple-masked · TreatmentPhase 2/3RecruitingDrug: COMP360 psilocybinPTSD - Post Traumatic Stress Disorder, PTSD, PTSD Symptoms, PTSD, Post Traumatic Stress Disorder300Nov 2028≤ 834 d2026-08-18
Efficacy, Safety, and Tolerability of Two Administrations of COMP360 in Participants With TRDNCT05711940COMP360 25 mg versus COMP360 1 mg for the change from baseline in MADRS total score.Randomized · Quadruple-masked · TreatmentPhase 3Active, not recruitingDrug: PsilocybinTreatment Resistant Depression5722025-11-13actual2026-08-10
A Phase II, Multicentre, Randomised, Double-blind, Controlled Study to Investigate the Safety, Tolerability, Pharmacokinetics, and Efficacy of COMP360 in Participants With Recurrent Major Depressive DisorderNCT05733546Safety and tolerability of COMP360 PsilocybinRandomized · Quadruple-masked · TreatmentPhase 2Active, not recruitingDrug: PsilocybinMajor Depressive Disorder102Sep 20252025-08-19
Efficacy, Safety, and Tolerability of COMP360 in Participants With TRDNCT05624268COMP360 25 mg versus placebo for the change from baseline in MADRS total scoreRandomized · Quadruple-masked · TreatmentPhase 3CompletedDrug: PsilocybinTreatment Resistant Depression2582025-05-28actual2026-08-10
Efficacy and Safety of COMP360 Psilocybin Therapy in Anorexia Nervosa: a Proof-of-concept StudyNCT05481736Change from baseline in the Eating Disorder Examination (EDE) global scoreRandomized · Quadruple-masked · TreatmentPhase 2CompletedDrug: PsilocybinAnorexia Nervosa322024-11-18actual2024-12-04
The Safety and Tolerability of COMP360 in Participants With Post-traumatic Stress DisorderNCT05312151results2025-06-13Number of Participants With Any Treatment-emergent Adverse Event (TEAE)Open-label · TreatmentStudy Protocol: v5.0 · Study Protocol: v4.0 · Study Protocol: v3.0 · Study Protocol: v2.0 · Study Protocol: v1.0 · Statistical Analysis Plan · Informed Consent FormPhase 2CompletedDrug: PsilocybinPost Traumatic Stress Disorder222024-02-12actual2025-06-13
Long Term Follow Up Study to COMP 001 And COMP 003 Trials (P-TRD LTFU)NCT04519957observationalLong-term efficacy of psilocybinCompletedTreatment Resistant Depression662022-08-11actual2022-09-22
The Safety and Efficacy Of Psilocybin as an Adjunctive Therapy in Participants With Treatment Resistant DepressionNCT04739865results2023-11-09Improvement in Depressive SymptomsOpen-label · TreatmentStudy Protocol · Statistical Analysis PlanPhase 2CompletedDrug: PsilocybinTreatment Resistant Depression192021-10-14actual2023-11-09
The Safety and Efficacy of Psilocybin in Participants With Treatment Resistant DepressionNCT03775200results2023-04-24Montgomery Asberg Depression Rating Scale (MADRS) Change From Baseline to Week 3Randomized · Quadruple-masked · TreatmentStudy Protocol · Statistical Analysis PlanPhase 2CompletedDrug: PsilocybinTreatment Resistant Depression2332021-07-30actual2023-04-24

Primary completion is the date the sponsor filed with the registry — their own projection, revised whenever they revise it, unless the row is marked actual.

Source: ClinicalTrials.gov, retrieved 2026-08-19