Octreotide
A somatostatin analog widely used in endocrine and neuroendocrine medicine, and one of the most important approved peptide drugs missing from many peptide libraries.
Also referenced as: Sandostatin, Sandostatin LAR
This peptide maps to at least one regulated medical product or label context in the United States.
This profile is grouped by its dominant research and market lane, not by vendor shelf placement.
Sandostatin, Sandostatin LAR
FDA label signal · 377 trials · 9612 PubMed results
Octreotide is an FDA-approved medicine with substantial published trial evidence. Note that research-market products sold under this name are not the approved medicine and are not held to the same manufacturing or labeling standards.
Octreotide has 49 name-matched clinical trials (3 international) (highest phase: Phase 4) and 9612 PubMed-indexed publications and holds an FDA drug label. 6 trials have posted results.
Re-checked nightly against the registries — tracked since 2026-07-09. No band changes yet.
Grades evidence strength, not efficacy or safety. Research-use context; not medical advice. Graded 2026-07-13 from PubMed, ClinicalTrials.gov, ISRCTN, openFDA, Health Canada, and OpenAlex — computed deterministically and refreshed nightly, with a retraction check. How we grade →
What octreotide is
Octreotide is a somatostatin analog used in regulated medicine for multiple endocrine and neuroendocrine indications.
Why it matters
It is one of the foundational approved peptide drugs and helps anchor the library in real peptide pharmacology beyond research-market compounds.
Regulatory context
Octreotide is FDA approved in the United States and exists in both immediate-release and long-acting forms.
Practical reading note
Octreotide is a reminder that some of the most important peptides in medicine are not trendy at all. They are just deeply established.