Definium Therapeutics Inc (DFTX) Stifel 2026 Virtual CNS Forum summary
Event summary combining transcript, slides, and related documents.
Stifel 2026 Virtual CNS Forum summary
8 Jul, 2026Pipeline and clinical development
Lead asset DT-120, a proprietary LSD tartrate, is in late-stage development for generalized anxiety disorder (GAD) and major depressive disorder (MDD), with pivotal data from three studies expected later this year.
Phase II data in GAD showed significant improvements in both anxiety and depression symptoms, supporting advancement to phase III and a breakthrough therapy designation for GAD.
Phase III studies are designed to demonstrate efficacy in broad patient populations, including those with prior treatment failures, and focus on both regulatory and payer requirements.
Durability of effect is a key focus, with primary endpoints at 6 weeks and extended observation to 12 weeks and beyond to assess long-term benefits.
Regulatory strategy includes comprehensive data collection on both anxiety and depression domains to support robust labeling and market access.
Study design and execution
Phase III GAD program includes two complementary studies: VOYAGE (100 mcg vs placebo) and PANORAMA (adds a 50 mcg decoy arm), both powered to detect a 5-point difference at high statistical power.
Blinded sample size re-estimation in VOYAGE showed better patient retention and lower variance, increasing power to 99% for detecting efficacy.
Multiple independent diagnostic and severity assessments are used at enrollment to ensure accurate patient selection and reduce risk from professional patients.
Continuous site engagement and internal review processes are in place to maintain study integrity and alignment with intended populations.
Commercial and market considerations
The eligible patient pool for DT-120 in MDD and GAD is estimated at 10–15 million, with even treating tens of thousands considered a significant impact.
The treatment model is designed for predictable, single-day inpatient stays, which is operationally attractive for providers and patients.
The company aims for broad market access and meaningful impact, not just niche adoption.
Latest events from Definium Therapeutics Inc
- DT120 ODT shows best-in-class efficacy and safety in MDD and GAD, supporting blockbuster potential.DFTX
Corporate presentation25 Jun 2026 - DT120 ODT showed rapid, durable efficacy and strong safety in Phase 3 MDD trials.DFTX
Study result22 Jun 2026 - Director elections, auditor appointment, and equity plan amendment approved; clinical trial results expected late Q2.DFTX
AGM 202611 Jun 2026 - Pivotal data for DT120 in GAD and MDD expected soon, with strong durability and remission seen.DFTX
Jefferies Global Healthcare Conference 20265 Jun 2026 - Phase III data for MDD and GAD are imminent, with strong regulatory and commercial readiness.DFTX
RBC Capital Markets Global Healthcare Conference 202619 May 2026 - Three pivotal Phase 3 readouts for DT120 ODT expected in 2026, with cash runway into 2028.DFTX
Q1 20268 May 2026 - DT120 ODT's late-stage trials target major psychiatric markets with strong efficacy and blockbuster potential.DFTX
Corporate presentation7 May 2026 - Virtual meeting to vote on directors, auditor, and equity plan; strong governance and pay practices.DFTX
Proxy filing27 Apr 2026 - Virtual meeting to vote on directors, auditor, and equity plan share increase.DFTX
Proxy filing27 Apr 2026