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Clinical Trial Details
A Multicenter, Double-Blind, Randomized, Parallel-Group, Placebo-Controlled, Study to Evaluate the Efficacy and Safety of Seltorexant 20 mg as Adjunctive Therapy to Antidepressants in Adult and Elderly Patients with Major Depressive Disorder with Insomnia Symptoms Who Have Responded Inadequately to Antidepressant Therapy and an Open-labeled Long-term Safety Extension Treatment with Seltorexant
Clinical Trial ( IRB ) #: W21-027-2
Title: A Multicenter, Double-Blind, Randomized, Parallel-Group, Placebo-Controlled, Study to Evaluate the Efficacy and Safety of Seltorexant 20 mg as Adjunctive Therapy to Antidepressants in Adult and Elderly Patients with Major Depressive Disorder with Insomnia Symptoms Who Have Responded Inadequately to Antidepressant Therapy and an Open-labeled Long-term Safety Extension Treatment with Seltorexant
Principal Investigator: Dr. Jayesh Kamath
Description: This is a clinical research study of an investigational medication for adults with Major Depressive Disorder (MDD). The purpose of this study is to evaluate its safety and effectiveness when it is used as an adjunct treatment in adults with MDD. Study participation will last up to 12 weeks. In some cases, you may have the option to continue participation for up to an additional 52 weeks. Qualified participants may receive investigational study medication and some study-related medical care at no cost. Participants may receive a stipend for completed in-person visits.
Classification:
  Psychiatry - General Adult/Mental Health (Depression, Anxiety, Etc.)
Eligibility Criteria: Adults 18-74 years of age; have been diagnosed with depression; have taken antidepressant treatment in the past that did not work well for them; are currently taking an antidepressant medication but still have symptoms of depression; for additional eligibility criteria, check with study contact
How to Contact: Galina Prpich. Telephone: 860-679-7539 Email: prpich@uchc.edu
Enrollment Status/Comments: Enrolling/recruiting