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Combined inhibition of tumor necrosis factor-alpha and interleukin12/23 for long-standing, refractory psoriatic disease: a differential role for cytokine pathways

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Its molecular structure includes: A 39-amino-acid backbone modeled on the natural GIP sequence Specific amino acid modifications that extend its biological half-life A fatty acid side chain (C20 diacid) attached via a linker, which allows it to bind to albumin in blood and further extend half-life Engineered receptor selectivity that produces balanced activation of both GLP-1 and GIP receptors These modifications don't change the fundamental classification