A second oral GLP-1 approval is anticipated in the first half of 2026 from Eli Lilly with orforglipron
The absence of a head-to-head trial means that prescribing decisions will initially be guided by availability, formulary coverage, individual tolerability, and prescriber familiarity rather than definitive comparative efficacy data
[5] Serum 25-hydroxyvitamin D, calcium, phosphate, and parathyroid hormone are re-examined at least eight weeks after each injection, and maintenance may shift to oral 1,000-2,000 IU daily once target levels (generally 30-50 ng mL ) are achieved, thereby reducing the risk of cumulative overdose while safeguarding skeletal health
LL-37 and human beta-defensins LL-37 is the only human cathelicidin, produced by keratinocytes, neutrophils, and mast cells in the skin