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These precise sequence structural enhancements dramatically elevate the compounds resistance to rapid enzymatic breakdown by serum proteases while magnifying its receptor binding affinity

If Phase 3 trials complete successfully and Lilly submits an NDA in late this year, FDA approval could come by mid to late next year

Its long-acting profile allows for convenient administration in extended research studies

The slow titration allows the body to adapt, reducing side effect severity compared to starting at higher doses

Rosenstock J, Nino A, Soffer J, Erskine L, Acusta A, Dole J, et al