NMDA Modulation in Antidepressant Nonresponders With Major Depressive Disorder

Who is this study for? Patients with Major Depressive Disorder
What treatments are being studied? NMDAE
Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Most of the current antidepressants for major depressive disorder (MDD) are based upon the monoamine hypothesis which cannot fully explain the etiology of depression. NMDA hypofunction has been implicated in the pathophysiology of depression. This study aims to examine the efficacy and safety of an NMDA enhancer (NMDAE) in the treatment of antidepressant nonresponders with MDD.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:

• Have a DSM-5 (American Psychiatric Association) diagnosis of MDD

• Have failed to respond to at least one antidepressant with adequate dosage and treatment duration

• Their original treatments should have been unchanged for at least 8 weeks. Some treatment-resistant patients (that is, having failed to respond to at least two different classes of antidepressants) who have started to refuse any antidepressant by themselves due to previous failure experience are also allowed, if they have already been antidepressant-free for at least 2 weeks

• 17-item Hamilton Rating Scale for Depression total score ≥ 18

• Agree to participate in the study and provide informed consent

Locations
Other Locations
Taiwan
Department of Psychiatry, China Medical University Hospital
RECRUITING
Taichung
Contact Information
Primary
Hsien-Yuan Lane, M.D., Ph.D
hylane@gmail.com
886 4 22052121
Time Frame
Start Date: 2022-01-25
Estimated Completion Date: 2026-12
Participants
Target number of participants: 50
Treatments
Experimental: NMDAE
An NMDA enhancer
Placebo_comparator: Placebo
Placebo
Related Therapeutic Areas
Sponsors
Leads: China Medical University Hospital

This content was sourced from clinicaltrials.gov