Content reviewed by clinical research staff

Last reviewed: March 2026Sources: PubMed, FDA, WADA Prohibited List

Evidence graded using the PeptideScholar A-D system

Lanreotide

AFDA Approved
65
Moderate Credibility
1 cited studyy · Evidence level A

Somatostatin analog · 8 amino acids · Brand: Somatuline Depot

FDA ApprovedPrescription Required

Lanreotide is a synthetic somatostatin analog approved by the FDA for gastroenteropancreatic neuroendocrine tumors (GEP-NETs) and acromegaly. It is a long-acting depot formulation given every 4 weeks.

Mechanism of Action

Binds to somatostatin receptors (primarily SSTR2 and SSTR5) on neuroendocrine tumor cells and pituitary somatotrophs. Inhibits secretion of growth hormone, insulin, glucagon, gastrin, serotonin, and VIP. In NETs, it controls hormone hypersecretion and has antiproliferative effects.

Benefits

  • First-line therapy for well-differentiated GEP-NETs (CLARINET trial)[1]
  • Prolongs progression-free survival in metastatic NETs[1]
  • Controls GH and IGF-1 in acromegaly
  • Deep subcutaneous autogel formulation
Not Medical Advice — Research-Reported Information Only

This content is for informational purposes only and does not constitute medical advice.

Lanreotide — Dosing in Published Research

Reported Routes: Subcutaneous injection
NETs: 120 mg deep subcutaneous every 4 weeks. Acromegaly: 90 mg every 4 weeks initially, titrated to 120 mg based on GH/IGF-1 response.

The dosing information above is sourced from published research literature and clinical trials. These are not recommendations. Individual responses vary. Always consult a healthcare provider before considering any peptide-based therapy.

Side Effects

  • GI symptoms (diarrhea, nausea, abdominal pain)
  • Gallstones and cholelithiasis (long-term use)
  • Hyperglycemia
  • Injection site reactions
  • Bradycardia

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Lanreotide is FDA-approved and available by prescription. Licensed telehealth providers can evaluate if it's right for you.

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Approved Treatment Routing

Lanreotide in PeptideScholar's current approved-treatment dataset

Lanreotide is currently modeled on this site as an approved treatment path for: Unresectable, well- or moderately-differentiated, locally advanced or metastatic gastroenteropancreatic neuroendocrine tumors; acromegaly. Brand names in the current dataset: Somatuline Depot.

Validation Note
This block reflects the site's current structured treatment data and internal routing logic. It is not a substitute for checking current prescribing, labeling, payer, or local regulatory details.

Research & Evidence

RCTN Engl J Med, 2014

Lanreotide in metastatic enteropancreatic neuroendocrine tumors.

Lanreotide 120 mg every 4 weeks significantly prolonged progression-free survival vs placebo in well-differentiated metastatic GEP-NETs

PMID: 25014687

References

  1. 1. Lanreotide in metastatic enteropancreatic neuroendocrine tumors.. N Engl J Med, 2014. Lanreotide 120 mg every 4 weeks significantly prolonged progression-free survival vs placebo in well-differentiated metastatic GEP-NETs [PMID: 25014687]

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Lanreotide FAQ

Medical Disclaimer

This content is for informational and educational purposes only and does not constitute medical advice, diagnosis, or treatment recommendations.

Always consult a qualified healthcare provider before starting, stopping, or modifying any treatment. Do not disregard professional medical advice based on information found on this site.

No claims of therapeutic efficacy are made for substances that are not FDA-approved for the discussed indications. Research citations reflect published findings and do not imply endorsement.

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