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SHP681 is a recombinant fusion protein that acts as a glucagon-like peptide 2 (GLP-2) analog fused to an Fc domain. It was developed for the treatment of gastrointestinal disorders, specifically short bowel syndrome. The drug functions as a modulator of the glucagon-like peptide 2 receptor (GLP-2R), aiming to enhance intestinal growth and function by mimicking endogenous GLP-2 activity. Originally developed by Shire and later Takeda following acquisition, SHP681 reached phase 1 clinical trials but development was discontinued after completion of early studies[1][3][6].
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