EICHORCondition: Generalized Anxiety Disorder · Sponsor: Intra-Cellular Therapies, Inc.
Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.
This is a multicenter, randomized, double-blind, placebo-controlled study evaluating the efficacy, safety, and tolerability of ITI-1284 compared with placebo as adjunctive therapy to GAD treatment in patients meeting Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, Text Revision (DSM-5-TR) criteria for GAD who have an inadequate response to ongoing GAD treatment.
This description comes directly from the study's public registry record.
ITI Clinical Trials · 6464409333 · ITCIClinicalTrials@itci-inc.com
Always discuss trial participation with your own doctor first.
| Clinical Site | Chandler, Arizona, United States | Active Not Recruiting |
| Clinical Site | Encino, California, United States | Recruiting |
| Clinical Site | Glendale, California, United States | Recruiting |
| Clinical Site | Imperial, California, United States | Recruiting |
| Clinical Site | Lemon Grove, California, United States | Recruiting |
| Clinical Site | Oceanside, California, United States | Recruiting |
| Clinical Site | Orange, California, United States | Recruiting |
| Clinical Site | Redlands, California, United States | Recruiting |
| Clinical Site | San Diego, California, United States | Active Not Recruiting |
| Clinical Site | Farmington, Connecticut, United States | Recruiting |
| Clinical Site | Gainesville, Florida, United States | Withdrawn |
| Clinical Site | Lauderhill, Florida, United States | Recruiting |
+ 57 more locations — full list on the registry record.
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This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.
Source record: clinicaltrials.gov/study/NCT06480383