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Lanreotide

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

IDDRUG-LANREOTIDE
TypeDrug
Aliases
Somatuline AutogelSomatuline DepotЛанреотид
Statusreviewed 2026-05-03 | pending_clinical_signoff
DiseasesDIS-GI-NET
SourcesSRC-NCCN-NET-2025

Drug Facts

ClassSomatostatin analogue (SSA)
MechanismLong-acting somatostatin analogue; high affinity for somatostatin receptor subtypes SSTR2 and SSTR5. Inhibits secretion of GH, IGF-1, insulin, glucagon, VIP, gastrin, and serotonin. Antiproliferative effect in well-differentiated GEP-NETs via SSTR2/SSTR5-mediated cell cycle arrest (CLARINET: HR 0.47 vs placebo). Symptom control in functional NETs (carcinoid syndrome: flushing, diarrhea).
Typical dosing120 mg SC deep subcutaneous injection every 4 weeks (q4w). Self-injection possible after training. Do not rub injection site. Alternate flanks/buttocks.
Ukraine registeredTrue
NSZU reimbursedFalse
Ukraine last verified2026-05-03

Notes

CLARINET (Caplin NEJM 2014): lanreotide 120 mg q4w vs placebo in well-differentiated G1/G2 non-functioning GEP-NET (n=204). mPFS not reached vs 18.0 mo (HR 0.47, p<0.001). 96-week extension (CLARINET OLE) confirmed durable benefit. FDA approved lanreotide for non-functioning GEP-NET 2014. PROMID (Rinke JCO 2009) with octreotide LAR established SSA antiproliferative class effect for midgut NETs.

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