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This distinction matters because ongoing provider relationships support medication adjustment, adverse event monitoring, and integration of biomarker dataparticularly important in GLP-1 therapy where dose titration and side-effect management require sustained clinical judgment

inked a potential $938 million licensing deal for APL-18881 (HEC-88473), Sunshines dual fibroblast growth factor 21 (FGF21)/glucagon-like peptide-1 (GLP-1) receptor agonist currently in a phase II study for type 2 diabetes

For the twin fetuses, arterial and venous catheters were placed in each twin as described above

Women should consult their healthcare provider about appropriate timing for discontinuation, as the medication has a half-life of approximately 5 days with elimination occurring over several weeks

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