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Semaglutide (2.4 mg obesity dose)

Deterministic view of the source YAML entity. Clinical authority remains with the cited source IDs and reviewer sign-off state.

IDDRUG-SEMAGLUTIDE-2-4MG
TypeDrug
Aliases
Semaglutide (2.4 mg)WegovyСемаглутид (2.4 мг — обезіта-доза)
Statusreviewed 2026-05-18 | pending_clinical_signoff
DiseasesNone declared
SourcesSRC-NCCN-BCELL-2025

Drug Facts

ClassGLP-1 receptor agonist (long-acting, once-weekly)
MechanismHuman glucagon-like peptide-1 analog (94% homology) with albumin- binding sidechain extending half-life to ~1 week. Activates GLP-1 receptors in pancreas (glucose-dependent insulin secretion + glucagon suppression), GI tract (delayed gastric emptying), and CNS (hypothalamic satiety signaling, reward-circuit modulation). At obesity dose (2.4 mg weekly), produces ~12-15% mean weight loss vs ~2-3% on placebo (STEP trials). Obesity is associated with ~13 cancers (IARC/WCRF) — sustained weight loss is a cancer-prevention intervention.
Typical dosingSC: dose escalation over 16-20 weeks to limit GI side effects: Week 1-4: 0.25 mg SC weekly Week 5-8: 0.5 mg SC weekly Week 9-12: 1.0 mg SC weekly Week 13-16: 1.7 mg SC weekly Week 17 onward: 2.4 mg SC weekly (maintenance) Inject SC abdomen / thigh / upper arm any day of the week; rotate sites.
Ukraine registeredTrue
NSZU reimbursedFalse
Ukraine last verified2026-05-18

Warnings

Notes

STUB — v0.2 prevention-workstream authoring; pending two-Clinical-Co-Lead signoff per CHARTER §6.1 dev-mode. Wegovy (semaglutide 2.4 mg) is first-in-class GLP-1 RA approved specifically for chronic obesity management. ~12-15% sustained weight loss in STEP trials. Obesity is associated with 13+ cancers per IARC/WCRF — pharmacotherapy is a recognized component of weight-loss strategy when behavioral approaches fail. Source cited is closest in-KB until USPSTF/AACE/WCRF obesity- pharmacotherapy sources land in source-stub workstream.

Used By

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