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LAR Lanreotide

Memorial Sloan Kettering Cancer Center · FDA-approved active Small molecule

Lanreotide is a somatostatin analog that binds to somatostatin receptors to inhibit the secretion of growth hormone and other hormones.

Lanreotide is a somatostatin analog that binds to somatostatin receptors to inhibit the secretion of growth hormone and other hormones. Used for Acromegaly, Gastroenteropancreatic neuroendocrine tumors (GEP-NETs), Carcinoid syndrome.

At a glance

Generic nameLAR Lanreotide
SponsorMemorial Sloan Kettering Cancer Center
Drug classSomatostatin analog
TargetSomatostatin receptors (SSTR2, SSTR5)
ModalitySmall molecule
Therapeutic areaOncology
PhaseFDA-approved

Mechanism of action

Lanreotide mimics somatostatin, a natural inhibitory hormone, by binding to somatostatin receptors (particularly SSTR2 and SSTR5) on neuroendocrine tumor cells and normal endocrine tissues. This binding suppresses the release of growth hormone, insulin-like growth factor-1 (IGF-1), and other hormones, thereby controlling hormone-related symptoms and slowing tumor growth in neuroendocrine malignancies.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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