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JM295 is a small molecule therapeutic candidate being developed by JMackem for the treatment of chronic pain. It functions as a dual-action agent, exhibiting antagonist activity against serotonin (5-HT) receptors and inhibiting the glycine transporter 2 (GlyT2). This dual mechanism is intended to modulate pain signaling within the central nervous system; GlyT2 inhibition increases synaptic glycine levels to enhance inhibitory neurotransmission in the spinal cord, while serotonin receptor antagonism targets the descending pain modulatory system. JM295 is currently in the preclinical stage of development.
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