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Pegvisomant

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

IDDRUG-PEGVISOMANT
TypeDrug
Aliases
SomavertПегвісомант
Statusreviewed 2026-07-11 | pending_clinical_signoff
DiseasesDIS-PITUITARY-ADENOMA
SourcesSRC-NCCN-CNS-2025

Drug Facts

ClassGrowth hormone receptor antagonist (PEGylated GH analog)
MechanismPEGylated recombinant human growth-hormone-receptor antagonist. Binds GH receptors and blocks GH-induced receptor dimerization and downstream signal transduction, lowering IGF-1 production without lowering circulating GH levels — it does not directly shrink the somatotroph adenoma. Used for biochemically persistent/residual acromegaly (elevated IGF-1) after transsphenoidal surgery and/or somatostatin-analogue therapy, either as an add-on to continuing SSA or as monotherapy when SSA is not tolerated or effective.
Typical dosingLoading dose 40 mg SC (under medical supervision), then 10 mg SC once daily; titrate in 5 mg increments every 4-6 weeks according to serum IGF-1, to a usual maintenance range of 10-30 mg/day (maximum 30 mg/day per product label). Confirm exact titration schedule with treating endocrinology team.
Ukraine registeredFalse
NSZU reimbursedFalse
Ukraine last verified2026-07-11

Notes

STUB pending clinical co-lead signoff (CHARTER §6.1 — dev-mode-exempted, safe to merge as draft content, not published/verified clinical advice). Pegvisomant is used for residual/persistent acromegaly per the Disease narrative, typically added to or substituted for somatostatin-analogue therapy after surgery. Does not lower GH/tumor size — IGF-1 is the biochemical target of titration.

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