Monotherapy of an NMDA Enhancer for Schizophrenia

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

Previous studies found that some NMDA-enhancing agent was able to augment antioxidant activity and its adjunctive therapy was better than placebo in reducing clinical symptoms and cognitive deficits and revealed favorable safety in patients with chronic schizophrenia. Of note, a substantial portion of schizophrenia patients refuse or cannot tolerate antipsychotics due to poor response or severe side effects. Therefore, this study aims to examine the efficacy and safety of an NMDA enhancer (NMDAE) as a monotherapy for the treatment of schizophrenia.

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

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

• Refuse or are unable to tolerate antipsychotics due to poor response or adverse effects

• PANSS total score ≥ 60

• Free of antipsychotic drugs for at least 1 week

• 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: 2018-01-01
Estimated Completion Date: 2025-12
Participants
Target number of participants: 80
Treatments
Experimental: NMDAE
An NMDA enhancer
Placebo_comparator: Placebo
Placebo
Related Therapeutic Areas
Sponsors
Collaborators: National Health Research Institutes, Taiwan
Leads: China Medical University Hospital

This content was sourced from clinicaltrials.gov

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