Lanreotide
Lanreotide, Somatuline Depot (lanreotide) is a protein pharmaceutical. Lanreotide was first approved as Somatuline depot on 2007-08-30. It is used to treat acromegaly and neuroendocrine tumors in the USA. The pharmaceutical is active against somatostatin receptor type 2 and somatostatin receptor type 5. In addition, it is known to target somatostatin receptor type 3.
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Commercial
Therapeutic Areas
Trade Name
FDA
EMA
Lanreotide, Somatuline depot
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Labels
FDA
EMA
Brand Name | Status | Last Update |
|---|---|---|
| lanreotide acetate | ANDA | 2025-02-01 |
| somatuline depot | New Drug Application | 2024-10-11 |
Indications
FDA
EMA
Indication | Ontology | MeSH | ICD-10 |
|---|---|---|---|
| neuroendocrine tumors | EFO_1001901 | D018358 | D3A.8 |
| acromegaly | — | D000172 | — |
Agency Specific
FDA
EMA
Expiration | Code | ||
|---|---|---|---|
LANREOTIDE ACETATE, SOMATULINE DEPOT, IPSEN PHARMA | |||
| 2024-09-15 | ODE-156 | ||
Patent Expiration
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Clinical
Clinical Trials
115 clinical trials
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Indications Phases 4
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Acromegaly | D000172 | — | — | 1 | 3 | 8 | 3 | 12 | 25 |
| Neuroendocrine tumors | D018358 | EFO_1001901 | D3A.8 | 1 | 6 | 3 | 2 | 12 | 23 |
| Carcinoid tumor | D002276 | — | D3A.00 | — | 2 | 3 | 1 | 1 | 7 |
| Circulating neoplastic cells | D009360 | — | — | — | — | — | 1 | — | 1 |
Indications Phases 3
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Pancreatic neoplasms | D010190 | EFO_0003860 | C25 | 1 | 2 | 1 | — | 2 | 5 |
| Stomach neoplasms | D013274 | EFO_0003897 | C16 | 1 | 1 | 1 | — | 2 | 4 |
| Intestinal neoplasms | D007414 | — | C26.0 | 1 | 1 | 1 | — | 2 | 4 |
| Malignant carcinoid syndrome | D008303 | — | E34.0 | — | — | 3 | — | 1 | 4 |
| Serotonin syndrome | D020230 | EFO_1001842 | G90.81 | — | — | 3 | — | 1 | 4 |
| Syndrome | D013577 | — | — | — | 1 | 2 | — | 1 | 4 |
| Liver diseases | D008107 | EFO_0001421 | K70-K77 | — | 3 | 3 | — | 1 | 4 |
| Autosomal dominant polycystic kidney | D016891 | EFO_1001496 | Q61.2 | — | 3 | 3 | — | 1 | 4 |
| Neoplasms | D009369 | — | C80 | — | 2 | 1 | — | — | 3 |
| Intestinal obstruction | D007415 | — | K56.60 | — | 2 | 1 | — | — | 3 |
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Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Dumping syndrome | D004377 | EFO_1001307 | K91.1 | — | 1 | — | — | — | 1 |
| Gastrointestinal neoplasms | D005770 | — | C26.9 | — | 1 | — | — | — | 1 |
| Digestive system neoplasms | D004067 | — | — | — | 1 | — | — | — | 1 |
| Pheochromocytoma | D010673 | — | — | — | 1 | — | — | — | 1 |
| Paraganglioma | D010235 | — | — | — | 1 | — | — | — | 1 |
| Intestinal diseases | D007410 | — | K63.9 | — | 1 | — | — | — | 1 |
| Gastrointestinal motility | D005769 | — | — | — | 1 | — | — | — | 1 |
| Graves ophthalmopathy | D049970 | EFO_1001466 | — | — | 1 | — | — | — | 1 |
| Eye diseases | D005128 | EFO_0003966 | H44 | — | 1 | — | — | — | 1 |
| Thyroid diseases | D013959 | — | E00-E07 | — | 1 | — | — | — | 1 |
Indications Phases 1
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Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
| Drug common name | Lanreotide |
| INN | lanreotide |
| Description | LANREOTIDE |
| Classification | Peptide |
| Drug class | peptides: inhibition of growth hormone release |
| Image (chem structure or protein) |  |
| Structure (InChI/SMILES or Protein Sequence) | CC(C)[C@@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@@H](NC(=O)[C@H](N)Cc2ccc3ccccc3c2)CSSC[C@@H](C(=O)N[C@H](C(N)=O)[C@@H](C)O)NC1=O |
Identifiers
| PDB | — |
| CAS-ID | 108736-35-2 |
| RxCUI | — |
| ChEMBL ID | CHEMBL1201185 |
| ChEBI ID | — |
| PubChem CID | 71349 |
| DrugBank | DB06791 |
| UNII ID | 0G3DE8943Y (ChemIDplus, GSRS) |
Target
Variants
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Trends
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Safety
Black-box Warning
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Adverse Events
Top Adverse Reactions
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9,152 adverse events reported
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