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Somatostatin analog

The Netherlands Cancer Institute · FDA-approved active Small molecule

Somatostatin analogs bind to somatostatin receptors on neuroendocrine tumor cells and other tissues, inhibiting hormone secretion and slowing tumor growth.

Somatostatin analogs bind to somatostatin receptors on neuroendocrine tumor cells and other tissues, inhibiting hormone secretion and slowing tumor growth. Used for Neuroendocrine tumors (gastroenteropancreatic and thoracic), Acromegaly, Variceal bleeding in portal hypertension.

At a glance

Generic nameSomatostatin analog
Also known aslanreotide, octreotide, sandostatin, somatuline, Arm A
SponsorThe Netherlands Cancer Institute
Drug classSomatostatin receptor agonist
TargetSomatostatin receptors (SSTR2, SSTR5)
ModalitySmall molecule
Therapeutic areaOncology
PhaseFDA-approved

Mechanism of action

Somatostatin analogs are synthetic derivatives of the natural hormone somatostatin that activate somatostatin receptors (particularly SSTR2 and SSTR5) on neuroendocrine cells. This activation suppresses the release of various hormones and growth factors, reducing symptoms from hormone excess and slowing proliferation of somatostatin receptor-positive tumors. They are commonly used in neuroendocrine tumors and gastroenteropancreatic neuroendocrine neoplasms.

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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