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Somatostatin (octreotide)

University Hospital Freiburg · Phase 3 active Small molecule

Octreotide is a somatostatin analog that binds to somatostatin receptors on neuroendocrine cells and blood vessels to inhibit the secretion of various hormones and reduce blood flow to tumors.

Octreotide is a somatostatin analog that binds to somatostatin receptors on neuroendocrine cells and blood vessels to inhibit the secretion of various hormones and reduce blood flow to tumors. Used for Neuroendocrine tumors (carcinoid syndrome, VIPomas, gastrinomas), Acromegaly, Variceal bleeding in portal hypertension.

At a glance

Generic nameSomatostatin (octreotide)
SponsorUniversity Hospital Freiburg
Drug classSomatostatin analog
TargetSomatostatin receptors (SSTR2, SSTR5)
ModalitySmall molecule
Therapeutic areaOncology; Endocrinology
PhasePhase 3

Mechanism of action

Octreotide mimics the natural hormone somatostatin by binding to somatostatin receptors (particularly SSTR2 and SSTR5) on neuroendocrine tumor cells and surrounding tissues. This binding suppresses the release of growth hormone, insulin, glucagon, and other hormones, while also causing vasoconstriction that reduces blood supply to tumors. The drug is used both therapeutically to control hormone-related symptoms and diagnostically in somatostatin receptor scintigraphy.

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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