ENCALM: A Study of ENX-102 as a Monotherapy Treatment in Patients With Generalized Anxiety Disorder (ENCALM)
Generalized Anxiety Disorder
About this trial
This is an interventional treatment trial for Generalized Anxiety Disorder
Eligibility Criteria
Key Inclusion Criteria: Male or female at birth, inclusive of any gender identity, aged 18 to 65 years, inclusive, at Screening Diagnosed with GAD according to the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5), confirmed by a Mini-International Neuropsychiatric Interview (MINI) version 7.0.2 Experiencing clinically significant generalized anxiety in need of treatment as measured by Hamilton Anxiety Rating Scale (HAM-A) Screening and Day 1 scores ≥22 and at least moderately severe score symptoms of anxious mood and tension as measured by HAM-A items 1 and 2, respectively, with score each ≥2 at Screening and Day 1 Key Exclusion Criteria: Clinically predominant psychiatric diagnosis other than GAD as confirmed by the MINI Clinically significant psychiatric co-morbidities as assessed by the MINI Reports moderately severe to severe symptoms of depression Ingested psychotropic medication within 5 half-lives or 21 days (whichever is longer) prior to Day 1, including THC and CBD, and unwillingness to refrain from their use for the entire duration of the trial Recent suicidal ideation or behavior Current or recent moderate to severe substance use disorder as assessed by the MINI Clinically significant abnormal findings in safety assessments Has significant progressive disorders or unstable medical conditions Unable to comply with the requirements of the study or, in the opinion of the Investigator or Sponsor, is unsuitable for the study
Sites / Locations
- Woodland International Research GroupRecruiting
- Woodland Research NorthwestRecruiting
- ProScience Research GroupRecruiting
- Collaborative Neuroscience Research, LLC (CNS)Recruiting
- Sunwise Clincial ResearchRecruiting
- Synergy Research Center - San DiegoRecruiting
- NRC Research InstituteRecruiting
- Excell Research, Inc.Recruiting
- Anderson Clinical ResearchRecruiting
- California Neuroscience Research, LLCRecruiting
- Vertex Clinical ResearchRecruiting
- Clinical Neuroscience Solutions, Inc.Recruiting
- Clinical Neuroscience Solutions, Inc.Recruiting
- CenExel iResearch, LLCRecruiting
- Collective Medical ResearchRecruiting
- Boston Clinical TrialsRecruiting
- ActivMed Practices & ResearchRecruiting
- Cenexel HRIRecruiting
- SPRI Clinical Trials, LLCRecruiting
- Clinical Neuroscience Solutions, Inc.Recruiting
- Austin Clinical Trials PartnersRecruiting
- FutureSearch Trials of DallasRecruiting
- Baylor College of MedicineRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
ENX-102
Placebo
Four weeks of 2 mg of ENX-102 in capsule form followed by 3 weeks of tapered dose plus 2 weeks of placebo in capsule form (before and/or after the ENX-102 treatment period), taken orally once daily in the evening for a 9-week total treatment period.
Nine weeks of placebo in capsule form taken orally once daily in the evening for a 9-week total treatment period.