Skip to main content
. Author manuscript; available in PMC: 2015 Jan 1.
Published in final edited form as: Annu Rev Pharmacol Toxicol. 2014;54:119–139. doi: 10.1146/annurev-pharmtox-011613-135950

Table 3.

Future directions for NMDA receptor antagonists in clinical depression research

Antidepressant dose-response testing
Further testing of strategies to augment and/or maintain antidepressant response
Continued validation and qualification of biomarkers of antidepressant response with goal of surrogate endpoints
Alternative means of administration, e.g., oral, intramuscular, and intranasal administration
Drug development/testing of more specific compounds, e.g., NR2B-selective antagonists, for improved efficacy and/or decreased psychotomimetic and other adverse effects
Assessment of the long-term risks of repeated NMDA receptor antagonist administration in supervised settings
Psychoeducation of psychiatric clinicians, patients, and society about the potential risks of NMDA receptor antagonists in nonsupervised settings