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Hormones & reproductionSomatostatin analog

Octreotide

Also known as: Sandostatin, Sandostatin LAR Depot, Mycapssa, SMS 201-995

By the Peptide Dossier Editorial TeamUpdated How we source

Octreotide is a long-acting somatostatin analog used for hormone-excess conditions. Its injectable, depot and selected oral-maintenance roles differ, as do symptom control, biochemical effects and tumor-progression outcomes.

Quick Facts

Class:Somatostatin analog
Product status:Approved octreotide products treat specific hormone-excess conditions; oral maintenance eligibility differs from injectable uses.
Research context:FDA approved

Somatostatin analog and product forms

Octreotide is a synthetic cyclic octapeptide developed as SMS 201-995. Natural somatostatin is degraded within minutes; the analog lasts longer and permits practical treatment. Product forms include Sandostatin injection, Sandostatin LAR Depot and oral Mycapssa.

Suppression of excess hormone secretion

Octreotide mainly binds somatostatin receptor subtype 2. It suppresses growth hormone/IGF-1 and gastrointestinal mediators including serotonin, VIP and gastrin. In acromegaly this improves biochemical control and symptoms and can reduce pituitary-tumor size. In carcinoid syndrome it relieves flushing/diarrhea by reducing hormone output, and in VIPoma it controls severe secretory diarrhea. Symptom control is distinct from a universal tumor-shrinkage claim.

In metastatic midgut neuroendocrine tumors, PROMID found median time to tumor progression of 14.3 months with long-acting depot versus 6.0 months with placebo. That antiproliferative outcome is a named trial result, not an approved indication for every formulation or every neuroendocrine tumor.

Supporting references: progression.

Sources: [1]

Approval and maintenance distinctions

FDA approved short-acting Sandostatin in 1988, followed roughly a decade later by monthly LAR Depot. Mycapssa was approved in 2020 for maintenance in acromegaly after response and tolerance to injectable somatostatin analogs. Depot and oral options can reduce the need for multiple daily injections, but their labeled eligibility and instructions remain product-specific.

Supporting references: approved.

Sources: [2]

Clinical uses

Uses include acromegaly and control of carcinoid flushing/diarrhea or VIPoma-associated profuse diarrhea. The oral maintenance population is specifically people with acromegaly already responding to and tolerating injectable analogs, rather than a generic oral substitute for every use.

Gastrointestinal, biliary, glucose and cardiac effects

Diarrhea, abdominal pain, nausea, gas, injection-site pain, gallstones/biliary sludge and high or low glucose are reported. Longer treatment can produce gallbladder disease; glucose and thyroid function can change. Bradycardia and cardiac-conduction effects are additional serious considerations.

References and further reading

This reference draws on Superpower’s Peptide Library and the research linked below. Peptide Dossier’s editorial team adapted and integrated the material on .

  1. 10.1200/JCO.2009.22.8510Suppression of excess hormone secretionCited in: Suppression of excess hormone secretion
  2. novartis.comApproval and maintenance distinctionsCited in: Approval and maintenance distinctions

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Disclaimer: This article is for informational and educational purposes only. It is not intended as medical advice. The information presented is based on published research and should not be used as a substitute for professional medical guidance. Always consult a qualified healthcare provider before starting any peptide protocol. Some peptides discussed may not be approved for human use by the FDA or equivalent regulatory bodies.