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Lanreotide

Generic Name
Lanreotide
Brand Names
Somatuline
Drug Type
Small Molecule
Chemical Formula
C54H69N11O10S2
CAS Number
108736-35-2
Unique Ingredient Identifier
0G3DE8943Y

Overview

Lanreotide is a drug employed in the management of acromegaly (a hormonal condition caused by excess growth hormone) in addition to symptoms caused by neuroendocrine tumors, especially carcinoid syndrome. This drug is a long-acting analog of the drug somatostatin, a growth hormone inhibitor. Lanreotide is manufactured by the company, Ipsen Pharmaceuticals as lanreotide acetate, and marketed as Somatuline. It is approved in several countries worldwide, including the United Kingdom, Australia, and Canada. Lanreotide was first approved for use in the United States by the FDA on August 30, 2007.

Background

Lanreotide is a drug employed in the management of acromegaly (a hormonal condition caused by excess growth hormone) in addition to symptoms caused by neuroendocrine tumors, especially carcinoid syndrome. This drug is a long-acting analog of the drug somatostatin, a growth hormone inhibitor. Lanreotide is manufactured by the company, Ipsen Pharmaceuticals as lanreotide acetate, and marketed as Somatuline. It is approved in several countries worldwide, including the United Kingdom, Australia, and Canada. Lanreotide was first approved for use in the United States by the FDA on August 30, 2007.

Indication

Lanreotide is indicated for the long-term treatment of patients with acromegaly who have had an inadequate response to, or cannot be treated with, surgery and/or radiotherapy. It is also indicated in the treatment of adult patients with unresectable, well- or moderately-differentiated, locally advanced or metastatic gastroenteropancreatic neuroendocrine tumors (GEP-NETs) to improve progression-free survival. Lanreotide is additionally indicated for the treatment of adults with carcinoid syndrome - when used, it reduces the frequency of short-acting somatostatin analog rescue therapy.

Associated Conditions

  • Acromegaly
  • Carcinoid Syndrome
  • Unresectable, locally advanced enteropancreatic neuroendocrine tumors
  • Unresectable, locally advanced well- or moderately-differentiated Gastroenteropancreatic Neuroendocrine Tumors
  • Unresectable, metastatic enteropancreatic neuroendocrine tumors
  • Unresectable, metastatic well- or moderately-differentiated Gastroenteropancreatic Neuroendocrine Tumors

Clinical Trials

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Title
Posted
Study ID
Phase
Status
Sponsor
2016/03/03
Phase 2
Completed
2016/02/17
Phase 3
Terminated
2016/01/11
Phase 2
Completed
2015/07/09
Phase 3
Completed
2015/03/24
Phase 1
Completed
2015/02/19
Phase 2
Terminated
2015/01/30
Phase 2
Completed
University Hospital, Grenoble
2014/11/11
Phase 2
Terminated
Federation Francophone de Cancerologie Digestive
2014/10/27
Phase 2
Completed
2014/09/04
Phase 2
Completed

FDA Drug Approvals

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NMPA Drug Approvals

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