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Clinical Peptide Medicines

Octreotide

Also referenced as: Sandostatin

A somatostatin analogue used to control specific excess-hormone and secretory symptoms.

Evidence grade
AStrong Clinical Evidence

Strong Clinical Evidence

Regulatory status
FDA Approved for Specific Indication

FDA-approved formulations cover specified acromegaly and carcinoid or VIPoma symptom indications. One formulation’s indication does not apply automatically to all products.

Human data
Yes

Registered clinical trials exist

Last reviewed
October 27, 2026

Overview

A somatostatin analogue used to control specific excess-hormone and secretory symptoms.

FDA-approved formulations cover specified acromegaly and carcinoid or VIPoma symptom indications. One formulation’s indication does not apply automatically to all products.

Immediate-release, depot and other formulations have different labels; symptom control is not proof of tumor cure.

Why It's Being Studied

  • Acromegaly
  • Carcinoid symptoms
  • VIPoma symptoms

Mechanism of Action

In plain language

Somatostatin-receptor activation inhibits growth hormone and several gastrointestinal hormones.

Technical detail

Somatostatin-receptor activation inhibits growth hormone and several gastrointestinal hormones. Immediate-release, depot and other formulations have different labels; symptom control is not proof of tumor cure.

Interactive diagram

From molecular target to clinical evidence

Tap each stage to see what happens.

Molecular target: Identify the receptor, enzyme, microbial membrane or binding site for the particular compound.

Background: Clinical Peptide Medicines

Clinical peptide medicines include endocrine treatments, antimicrobial drugs, receptor blockers and targeted diagnostic or cancer agents. They do not share one mechanism or one set of indications.

An approval belongs to a specific medicine and indication. A diagnostic tracer, an antibiotic and a hormone are not interchangeable wellness products; read each profile's own mechanism and prescribing source.

Research Areas & Routes Studied

Areas studied
  • Acromegaly
  • Carcinoid symptoms
  • VIPoma symptoms
Routes used in research
  • Injectable approved formulations
  • Product-specific oral formulation

Evidence Summary

Human studies demonstrate biochemical and secretory-symptom control in the approved disease settings.

Evidence pyramid

Higher tiers carry more weight. Filled tiers have evidence for Octreotide; tap to read it.

Human clinical trials
  • Human studies demonstrate biochemical and secretory-symptom control in the approved disease settings.
Source breakdown

1 cited sources.

  • Prescribing label1

Human clinical evidence

  • Human studies demonstrate biochemical and secretory-symptom control in the approved disease settings.

Reported Adverse Events in Research

  • Gallstones, glucose changes, bradycardia and fat malabsorption are important adverse effects.

Limitations of Current Evidence

  • Immediate-release, depot and other formulations have different labels; symptom control is not proof of tumor cure.
  • Findings apply to the product, route and population studied; they do not establish benefits or safety for unrelated wellness uses or research-vial products.

How to Read This Research

Questions to ask
  • Is this a single molecule or a family of medicines?
  • Is the use diagnostic, therapeutic or investigational?
  • Does the quoted outcome match the exact product, formulation and population?
Reading tips
  • Use the compound-specific mechanism above; this diagram describes drug development, not a shared biological pathway.
  • Historical approval, present availability and off-label use are distinct questions.
  • For radiopharmaceuticals and hospital medicines, specialist handling is part of the treatment context.
Indication
The condition and population for which a medicine is approved.
Antagonist
A compound that blocks activity at a receptor.
Radiopharmaceutical
A medicine containing a radioactive isotope for imaging or treatment.

Compare With Other Compounds

Compare side by side
OctreotideTrofinetide
Evidence gradeA — Strong Clinical EvidenceB — Moderate Human Evidence
Regulatory statusFDA Approved for Specific IndicationFDA Approved for Specific Indication
Human dataYesYes
Clinical trialsRegistered trials existRegistered trials exist
Research routesInjectable approved formulations, Product-specific oral formulationOral approved medicine
Cited sources12
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Frequently Asked Questions

Research References

  • Prescribing label

    Octreotide — prescribing label

    View Source
This page is an educational research summary. It is not medical advice, does not recommend human use, and does not provide individualised dosing. Many compounds discussed here are research use only and are not approved medicines.