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Lanreotide

Also known as: Somatuline Depot, Somatuline Autogel, BIM 23014

A long-acting somatostatin analog for acromegaly and neuroendocrine tumors. FDA-approved as Somatuline Depot since 2007. Prescription medication.

Last updated

Mechanism of Action

Lanreotide is a cyclic octapeptide somatostatin analog with high affinity for somatostatin receptor subtypes 2 and 5. Binding inhibits growth hormone secretion from the pituitary, lowering IGF-1, and suppresses release of serotonin and other hormones from neuroendocrine tumors. It also has antiproliferative effects on gastroenteropancreatic neuroendocrine tumors. The depot formulation self-assembles into a gel after deep subcutaneous injection, releasing drug over about a month.

Half-life
~23 to 30 days (depot formulation)
Administration Routes
Subcutaneous
Research Status
Clinical

Reported Benefits

  • Approved for long-term treatment of acromegaly
  • Approved to improve progression-free survival in unresectable gastroenteropancreatic neuroendocrine tumors (CLARINET)
  • Approved to reduce the need for short-acting rescue therapy in carcinoid syndrome

Potential Side Effects

  • Diarrhea, abdominal pain, nausea and flatulence
  • Gallstones
  • Injection-site reactions
  • High or low blood glucose
  • Bradycardia

Common Dosing

Labeled dosing is a deep subcutaneous injection every 4 weeks, given by a healthcare provider or a trained patient or caregiver; the dose depends on the indication and, in acromegaly, on hormone levels. Dosing is set and supervised by the prescribing clinician.

The dosing information above is aggregated from research literature and anecdotal community reports for educational purposes only. It is not a recommendation, prescription, or medical advice. Peptides are sold as research chemicals only and are not intended for human use.

Contraindications

  • Known hypersensitivity to lanreotide
  • Use with caution in gallbladder disease, diabetes and cardiac conduction disorders
  • Lanreotide in metastatic enteropancreatic neuroendocrine tumors

    2014

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  • Rapid and sustained reduction of serum growth hormone and insulin-like growth factor-1 in patients with acromegaly receiving lanreotide Autogel therapy: a randomized, placebo-controlled, multicenter study with a 52 week open extension

    2010

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Yes. The FDA approved lanreotide as Somatuline Depot in 2007 for acromegaly, in 2014 for gastroenteropancreatic neuroendocrine tumors, and in 2017 for carcinoid syndrome. A lanreotide injection from a second manufacturer was approved in 2021.

Both are somatostatin analogs that act on the same receptor subtypes. Lanreotide's depot is given by deep subcutaneous injection every 4 weeks, while long-acting octreotide is an intramuscular monthly injection; short-acting and oral forms exist only for octreotide.

PeptideChat is for educational and research purposes only. Nothing on this site constitutes medical advice. Peptides are sold as research chemicals only and are not intended for human use. These statements have not been evaluated by the FDA and are not intended to diagnose, treat, cure, or prevent any disease. PeptideChat is an independent educational resource — not a pharmacy, compounding, or 503A/503B outsourcing facility — and does not sell products or provide medical advice.