MM120 · program

Lysergide D-tartrate (MM120 / LSD) for Major depressive disorder

Phase 3RecruitingDefinium Therapeutics, Inc. (DFTX)

Indications for MM120: Generalized anxiety disorder · Phase 3 Attention-deficit/hyperactivity disorder · Discontinued Major depressive disorder · Phase 3 Post-traumatic stress disorder · Phase 3

MM120 (DT120) for major depressive disorder — second indication after the lead GAD program. Phase 3 'Emerge' study (NCT06941844) evaluates a single dose for MDD. Builds on MM120's Phase 2b anxiety data and the GAD Phase 3 program (Voyage/Panorama).

Development timeline

Phase 3Sept 2025
  1. Phase 3 MDD program (Emerge, NCT06941844) initiated. Date approximate.

Clinical trials in Major depressive disorder

NCT07592689Phase 3Recruitingn=165

A Phase 3 Trial of DT120 for Major Depressive Disorder (Ascend)

Started May 2026· Primary completion Sept 2027· 📍 27 sites across 1 country (United States)

NCT06941844EmergePhase 3Recruiting

Phase 3 Study of MM120 (Lysergide) in Major Depressive Disorder (Emerge)

· 📍 25 sites across 1 country (United States)

Formulations

FormulationRouteRegimenPharmacokinetics
DT120 orally disintegrating tablet (ODT)Orally disintegrating tablet (ODT) using Catalent Zydis fast-dissolve technology
Proprietary orally disintegrating tablet of lysergide (LSD) D-tartrate; single administration; designed for faster absorption and onset
OralSingle dose

Mechanism of action (compound-wide)

LSD acts across serotonin receptor subtypes; the company describes MM120 as a 5-HT2A partial agonist (IUPHAR classifies LSD as a full 5-HT2A agonist). Antidepressant effects attributed primarily to 5-HT2A agonism.

TargetActionAffinity
5-HT2AprimaryHTR2APartial agonistpKi 9.4
5-HT1AHTR1AAgonistpKi 9
5-HT2CHTR2CAgonistpKi 8.2

← Full MM120 compound page (identity, identifiers, all indications)

Sources

  1. DT120 ODT — LSD Therapy for Depression and Anxiety — Definium Therapeutics
  2. clinicaltrials.gov — clinicaltrials.gov
  3. Lysergide (LSD), Ligand 17 — IUPHAR/BPS
  4. MM120 Emerge Phase 3 MDD (NCT06941844) — ClinicalTrials.gov