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Dulaglutide exploits this property of the Fc fragment to extend the half-life by linking the amino acid-substituted GLP-1 molecule to the N-terminal end of the Fc fragment via a 16-amino acid junction (Figure 2)
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L., Safieddine, S., Mustapha, M
Figure 1 Table 2 Adverse effects and safety risks in phase 3 trials ( AE, adverse event
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