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SYN116 is a small molecule drug that acts as an antagonist of the prostacyclin (PGI2) receptor, also known as the prostanoid IP receptor. It was initially developed by F. Hoffmann-La Roche and later involved organizations such as Acorda Therapeutics and Biotie Therapies Oy. The primary therapeutic area explored for SYN116 was nervous system diseases, with clinical development focused on pain management. Its mechanism involves blocking the PGI2 receptor to modulate pain signaling pathways in the nervous system. Development of SYN116 has been discontinued after reaching Phase 1 clinical trials[1].
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