Lanreotide
A long-acting somatostatin analog marketed as Somatuline Depot and used in neuroendocrine and acromegaly-related care.
Also referenced as: Somatuline Depot, Lanreotide Acetate
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.
Somatuline Depot, Lanreotide Acetate
FDA label signal · 124 trials · 1225 PubMed results
Lanreotide 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.
Lanreotide has 58 name-matched clinical trials (1 international) (highest phase: Phase 4) and 1225 PubMed-indexed publications and holds an FDA drug label. 19 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 lanreotide is
Lanreotide is a long-acting somatostatin analog best known in the United States as Somatuline Depot.
Why it matters
It rounds out the approved somatostatin-analog side of the peptide library and gives users a more complete picture of serious peptide therapeutics in endocrine medicine.
Regulatory context
Lanreotide is FDA approved in the United States.
Practical reading note
When a peptide has deep real-world use in medicine, it often deserves a page even if it is not a gray-market conversation magnet.