CERC-301

From WikiMD's Food, Medicine & Wellness Encyclopedia

CERC-301 is an investigational drug compound that has been explored for its potential therapeutic effects in various neurological and psychiatric conditions, most notably in the treatment of major depressive disorder (MDD) and suicidal ideation. It functions as an antagonist of the N-methyl-D-aspartate (NMDA) receptor, a subtype of glutamate receptors in the brain. By modulating these receptors, CERC-301 is thought to influence neurotransmission and neural plasticity, which are often dysregulated in mood disorders.

Mechanism of Action[edit | edit source]

CERC-301 selectively targets and inhibits the NMDA receptor, which plays a crucial role in synaptic transmission and plasticity. The NMDA receptor is involved in the pathophysiology of depression and is a target for the development of novel antidepressants. By inhibiting this receptor, CERC-301 may exert rapid antidepressant effects, potentially improving symptoms in individuals with treatment-resistant depression.

Clinical Trials[edit | edit source]

Several clinical trials have been conducted to evaluate the efficacy, safety, and tolerability of CERC-301 in treating MDD and suicidal ideation. Early phase trials suggested some potential benefits of CERC-301 in improving depressive symptoms. However, subsequent larger-scale studies were needed to fully understand its therapeutic profile and to determine its place in the treatment of mood disorders.

Potential Indications[edit | edit source]

While initially investigated for MDD and suicidal ideation, the scope of CERC-301's potential applications may extend to other conditions characterized by NMDA receptor dysregulation. These could include various forms of anxiety disorders, obsessive-compulsive disorder (OCD), and certain neurodegenerative diseases. Further research is necessary to explore these possibilities and to establish CERC-301's efficacy and safety in these contexts.

Safety and Tolerability[edit | edit source]

The safety profile of CERC-301 has been evaluated in clinical trials, with most adverse effects being mild to moderate in severity. Commonly reported side effects include headache, dizziness, and gastrointestinal disturbances. As with all investigational drugs, a thorough assessment of its safety, especially with long-term use, is critical before any potential approval for clinical use.

Current Status[edit | edit source]

As of the last update, CERC-301 remains an investigational drug. Its development for the treatment of MDD and other psychiatric or neurological conditions is contingent upon the outcomes of ongoing and future clinical trials. The drug's path to potential approval will depend on demonstrating a favorable balance of efficacy and safety in a larger patient population.

See Also[edit | edit source]

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Contributors: Prab R. Tumpati, MD