Frontlight ResearchEarly access
Active, not recruitingPhase 3
A Phase 3 Trial of MM120 for Generalized Anxiety Disorder (Panorama)
Key facts
- Who runs it
- Definium Therapeutics US, Inc.
- Where
- Atlanta, Austin, Boston, Bradenton, Cincinnati, Everett, Little Rock, Los Angeles, North Canton, Orlando, Princeton, and Towson, United StatesSee the 13 sitesAlso in 5 other countries, 22 sites
- Trial code
- NCT06809595
- EU 2024-513572-17-00
- U1111-1309-7563
- Status
- Active, not recruiting
- Phase
- Phase 3
- People taking part
- 245 people enrolled
- Started
- 29 Jan 2025
- Expected to end
- May 2027
- Type of study
- Interventional, 3 groupsOne group gets a placebo (a dummy treatment), for comparison.
- Treatments tested
- Placebo
- DT120
- Record updated
- 4 September 2026
Who can take part
- Age
- 18 years to 74 years
- Sex
- Women and men
- Healthy volunteers
- Cannot take part
The registry criteria, word for word
Show all 7 criteriaShow less
Who can take part
- Diagnosis of GAD per DSM-5
- Male or female aged 18 to 74
- HAM-A Total Score ≥20
Who cannot take part
- Certain psychiatric disorders (other than generalized anxiety disorder)
- First degree relative with or lifetime history of a psychotic disorder or bipolar disorder
- Current diagnosis of alcohol or substance use disorder (excluding nicotine and caffeine)
- Any clinically significant unstable illness
Where in United States
Also in 5 other countries, 22 sites
- Atlanta Center for Medical ResearchAtlanta, United States
- Austin Clinical Trial PartnersAustin, United States
- Adams Clinical BostonBoston, United States
- Bradenton Research Center, Inc.Bradenton, United States
- University of Cincinnati Psychiatry- Anxiety Disorders Research ProgramCincinnati, United States
- Core Clinical ResearchEverett, United States
- Preferred Research Partners, IncLittle Rock, United States
- Psychedelic Science InstituteLos Angeles, United States
- West Los Angeles VA Medical CenterLos Angeles, United States
- Neuro-Behavioral Clinical Research Inc.North Canton, United States
- Clinical Neuroscience Solutions, Inc.Orlando, United States
- Princeton Medical InstitutePrinceton, United States
- Sheppard Pratt Health SystemTowson, United States
About the trial
What the trial wants to find out
A Phase 3, Double-blind, Placebo-controlled Study (Part A) with an Open-label Extension (Part B) Evaluating DT120 Compared to Placebo in Generalized Anxiety Disorder - Panorama
The 3 groups in the trial
- Arm 1 - PlaceboPlacebo, for comparison
A substance that is designed to have no therapeutic value
Treatment: Placebo
- Arm 2 - 50µg DT120Sham treatment, for comparison
A psychoactive substance that mediates effects mainly through an agonist activity in the serotonin 2A receptor (5-HT2A)
Treatment: DT120
- Arm 3 - 100µg DT120Treatment being tested
A psychoactive substance that mediates effects mainly through an agonist activity in the serotonin 2A receptor (5-HT2A)
Treatment: DT120
Data and sources
- Registry record
- Listed on ClinicalTrials.gov and on the EU's official list of trials (CTIS).
- Official title
- 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 - Panorama
- Publications
- Psychedelic medicine: mechanisms, evidence, and translation to practice.BMJ (Clinical research ed.), 2026
- Record updated
- 4 September 2026