Lutetium dotatate lu-177
EndolucinBeta, Lumark (lutetium dotatate lu-177) is an unknown pharmaceutical. Lutetium dotatate lu-177 was first approved as Lumark on 2015-06-18. It has been approved in Europe to treat radionuclide imaging.
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Therapeutic Areas
Therapeutic Area | MeSH |
|---|---|
| diagnosis | D003933 |
Trade Name
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Drug Products
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New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
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Labels
FDA
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Indications
FDA
EMA
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Agency Specific
FDA
EMA
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Patent Expiration
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HCPCS
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Clinical
Clinical Trials
69 clinical trials
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Indications Phases 4
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Papillary thyroid cancer | D000077273 | — | — | — | 1 | — | 1 |
Indications Phases 3
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Neuroendocrine tumors | D018358 | EFO_1001901 | D3A.8 | 13 | 19 | 6 | — | 8 | 40 |
| Carcinoid tumor | D002276 | D3A.00 | — | 3 | 1 | — | — | 4 |
Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Neuroendocrine carcinoma | D018278 | 1 | 6 | — | — | — | 6 | ||
| Pancreatic neoplasms | D010190 | EFO_0003860 | C25 | 3 | 4 | — | — | 1 | 6 |
| Paraganglioma | D010235 | 1 | 4 | — | — | — | 4 | ||
| Pheochromocytoma | D010673 | 1 | 3 | — | — | — | 3 | ||
| Meningioma | D008579 | EFO_0003098 | D32.9 | 1 | 3 | — | — | — | 3 |
| Neoplasms | D009369 | C80 | — | 2 | — | — | 1 | 3 | |
| Merkel cell carcinoma | D015266 | EFO_1001471 | C4A | 1 | 2 | — | — | — | 2 |
| Neuroblastoma | D009447 | EFO_0000621 | 1 | 1 | — | — | — | 2 | |
| Breast neoplasms | D001943 | EFO_0003869 | C50 | — | 1 | — | — | — | 1 |
| Pituitary neoplasms | D010911 | — | 1 | — | — | — | 1 |
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Indications Phases 1
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Thymoma | D013945 | 1 | — | — | — | — | 1 | ||
| Mesothelioma | D008654 | C45 | 1 | — | — | — | — | 1 | |
| Glioblastoma | D005909 | EFO_0000515 | 1 | — | — | — | — | 1 |
Indications Without Phase
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Stomach neoplasms | D013274 | EFO_0003897 | C16 | — | — | — | — | 1 | 1 |
| Gastrointestinal neoplasms | D005770 | C26.9 | — | — | — | — | 1 | 1 | |
| Digestive system neoplasms | D004067 | — | — | — | — | 1 | 1 | ||
| Gastrointestinal diseases | D005767 | — | — | — | — | 1 | 1 | ||
| Germ cell and embryonal neoplasms | D009373 | — | — | — | — | 1 | 1 | ||
| Endocrine system diseases | D004700 | EFO_0001379 | E34.9 | — | — | — | — | 1 | 1 |
| Neoplasms by histologic type | D009370 | — | — | — | — | 1 | 1 | ||
| Intestinal neoplasms | D007414 | C26.0 | — | — | — | — | 1 | 1 | |
| Endocrine gland neoplasms | D004701 | EFO_0003769 | D35 | — | — | — | — | 1 | 1 |
| Neoplasms by site | D009371 | — | — | — | — | 1 | 1 |
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Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
| Drug common name | LUTETIUM DOTATATE LU-177 |
| INN | lutetium (177lu) oxodotreotide |
| Description | Lutetium (177Lu) oxodotreotide (INN) or 177Lu DOTA-TATE, trade name Lutathera, is a chelated complex of a radioisotope of the element lutetium with DOTA-TATE, used in peptide receptor radionuclide therapy (PRRT). Specifically, it is used in the treatment of cancers which express somatostatin receptors.
|
| Classification | Small molecule |
| Drug class | Antineoplastic agent |
| Image (chem structure or protein) | |
| Structure (InChI/SMILES or Protein Sequence) | — |
Identifiers
| PDB | — |
| CAS-ID | 437608-50-9 |
| RxCUI | — |
| ChEMBL ID | CHEMBL3989924 |
| ChEBI ID | — |
| PubChem CID | — |
| DrugBank | DB13985 |
| UNII ID | AE221IM3BB (ChemIDplus, GSRS) |
Target
Agency Approved
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Alternate
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Variants
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Trends
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Additional graphs summarizing 55 documents
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Safety
Black-box Warning
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Adverse Events
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23 adverse events reported
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