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A Phase 3, Multicenter, Randomized, Double-blind, Placebo-controlled, 12-Week Study (Part A) With a 40-Week Open-label Extension (Part B) Evaluating the Efficacy and Safety of Oral MM120 Compared to Placebo in the Treatment of Adults With Generalized Anxiety Disorder - Voyage

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Trial Profile

A Phase 3, Multicenter, Randomized, Double-blind, Placebo-controlled, 12-Week Study (Part A) With a 40-Week Open-label Extension (Part B) Evaluating the Efficacy and Safety of Oral MM120 Compared to Placebo in the Treatment of Adults With Generalized Anxiety Disorder - Voyage

Status: Active, no longer recruiting
Phase of Trial: Phase III

Latest Information Update: 28 Apr 2026

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At a glance

  • Drugs Lysergic acid diethylamide MindBio Therapeutics (Primary)
  • Indications Generalised anxiety disorder
  • Focus Registrational; Therapeutic Use
  • Acronyms VOYAGE
  • Sponsors Definium Therapeutics

Most Recent Events

  • 22 Apr 2026 According to Definium Therapeutics media release, enrollment complete with 214 patients .
  • 22 Apr 2026 Status changed from recruiting to active, no longer recruiting.
  • 26 Feb 2026 According to Definium Therapeutics media release, the study enrollment is approximately 80% complete and is expected to conclude in the coming weeks. Topline data are anticipated in early 3Q 2026. The protocol-specified blinded sample size re-estimation is complete, requiring no increase in enrollment. Voyage is expected to enroll approximately 200 participants in the U.S. randomized 1:1 to receive DT120 ODT 100 µg or placebo.

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