Biopharma Transcript

COMPASS Pathways plc CMPS

Nasdaq · Phase 3 · CNS/neurology/psychiatry · small molecule · EDGAR · Updated Oct 24, 2026

COMPASS Pathways plc (Nasdaq: CMPS) is a CNS/neurology/psychiatry drug developer. Its lead program, COMP360 psilocybin treatment, is in Phase 3 for Treatment-resistant depression (TRD). Its next catalyst on record is COMP360 in TRD: Potential FDA approval and first product revenue (2027).

Upcoming catalysts

No catalyst is dated to the next 30 days or to an FDA action date.

Next further out: COMP360 in TRD — Potential FDA approval and first product revenue (2027). 1 catalyst on record beyond the next 30 days; subscribers see each with its filing sentence.

Pipeline

ProgramIndicationModalityStage
COMP360 (COMP005 and COMP006 pivotal trials)Treatment-resistant depressionsmall moleculePhase 3
COMP360 (COMP202)PTSDsmall moleculePhase 2

Recent results and decisions

  1. Aug 5, 2026
    started Late-stage (Phase 2b/3) PTSD trial is underway.Compass continues to progress PTSD program, with late-stage trial underway. Filing
  2. Jul 7, 2026
    positive 26-week data from COMP006 and COMP005 show rapid onset and durability through at least 6 months; primary endpoint at Week 6 previously met (P<0.001) in both trials.COMP006 and COMP005 26-week data demonstrate rapid onset and remarkable durability through at least 6 months further validating COMP360’s differentiated profile in highly chronic TRD Filing
  3. May 13, 2026
    accepted FDA granted rolling NDA submission and review; sections of the NDA already submitted, final submission on track for Q4 2026.FDA granted Compass NDA rolling submission and review request, based on strength of positive Phase 3 data. Filing

3 more on record.

For subscribers

Other phase 3 CNS/neurology/psychiatry companies