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Torisel(temsirolimus)
Torisel (temsirolimus) is a small molecule pharmaceutical. Temsirolimus was first approved as Torisel on 2007-05-30. It is used to treat renal cell carcinoma in the USA. It has been approved in Europe to treat mantle-cell lymphoma and renal cell carcinoma. The pharmaceutical is active against serine/threonine-protein kinase mTOR.
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
neoplasmsD009369
urogenital diseasesD000091642
hemic and lymphatic diseasesD006425
immune system diseasesD007154
Trade Name
FDA
EMA
Torisel (generic drugs available since 2018-07-30)
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Temsirolimus
Tradename
Company
Number
Date
Products
TORISELCV SciencesN-022088 RX2007-05-30
1 products, RLD, RS
Labels
FDA
EMA
Brand Name
Status
Last Update
toriselNew Drug Application2019-12-05
Indications
FDA
EMA
Indication
Ontology
MeSH
ICD-10
renal cell carcinomaEFO_0000376D002292
Agency Specific
FDA
EMA
No data
Patent Expiration
Patent
Expires
Flag
FDA Information
Temsirolimus, Torisel, Pf Prism Cv
87910972032-05-10U-1550, U-1551
80262762026-01-20DP
82991162023-07-25DP
84555392023-07-25DP
87227002023-07-25DP
ATC Codes
L: Antineoplastic and immunomodulating agents
L01: Antineoplastic agents
L01E: Protein kinase inhibitors, antineoplastic and immunomodulating agents
L01EG: Mammalian target of rapamycin (mtor) kinase inhibitors
L01EG01: Temsirolimus
HCPCS
Code
Description
J9330
Injection, temsirolimus, 1 mg
Clinical
Clinical Trials
367 clinical trials
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Mock data
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Kidney transplantationD01603022610
Coronary diseaseD003327729
Non-hodgkin lymphomaD008228C85.93618
Graft vs host diseaseD006086D89.8113328
Renal insufficiencyD051437HP_0000083N19123
Kidney diseasesD007674EFO_0003086N08112
Communicable diseasesD00314111
Virus diseasesD014777B3411
InflammationD00724911
Graft rejectionD00608411
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Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Renal cell carcinomaD00229212133529
Prostatic neoplasmsD011471C6110101116
Breast neoplasmsD001943EFO_0003869C5087215
Mantle-cell lymphomaD020522C83.146129
Kidney neoplasmsD007680EFO_0003865C6443119
Liver neoplasmsD008113EFO_1001513C22.05519
Tuberous sclerosisD014402HP_0009720Q85.11537
Type 1 diabetes mellitusD003922EFO_0001359E101416
LymphomaD008223C85.9415
AngiofibromaD018322EFO_10017612225
Show 15 more
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
NeoplasmsD009369C80507357
SarcomaD0125097812
MelanomaD0085456812
Endometrial neoplasmsD016889EFO_00042307411
Non-small-cell lung carcinomaD0022898510
GlioblastomaD005909EFO_0000515779
Ovarian neoplasmsD010051EFO_0003893C56448
Multiple myelomaD009101C90.0457
Pancreatic neoplasmsD010190EFO_0003860C25447
GliosarcomaD018316567
Show 88 more
Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Lung neoplasmsD008175C34.9022
Immunosuppression therapyD007165112
Port-wine stainD019339Q82.522
Digestive system neoplasmsD00406711
Respiratory tract neoplasmsD012142EFO_0003853D1411
Castleman diseaseD005871EFO_1001332D47.Z211
Soft tissue neoplasmsD01298311
Neurofibromatosis 2D016518Q85.0211
Pharyngeal neoplasmsD010610C14.011
Erdheim-chester diseaseD03124911
Show 36 more
Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Coronary artery diseaseD003324I25.133
Insulin resistanceD007333EFO_000261422
Heart diseasesD006331EFO_0003777I51.911
Crohn diseaseD003424EFO_0000384K5011
Thrombocytopenic purpura idiopathicD016553EFO_0007160D69.311
Post-traumatic stress disordersD013313EFO_0001358F43.111
Coronary stenosisD023921EFO_100088211
Muscular atrophyD009133HP_000320211
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameTEMSIROLIMUS
INNtemsirolimus
Description
Temsirolimus, sold under the brand name Torisel, is an intravenous drug for the treatment of renal cell carcinoma (RCC), developed by Wyeth Pharmaceuticals and approved by the U.S. Food and Drug Administration (FDA) in May 2007, and was also approved by the European Medicines Agency (EMA) in November 2007. It is a derivative and prodrug of sirolimus.
Classification
Small molecule
Drug classimmunosuppressives
Image (chem structure or protein)
Structure (InChI/SMILES or Protein Sequence)
CO[C@H]1C[C@@H]2CC[C@@H](C)[C@@](O)(O2)C(=O)C(=O)N2CCCC[C@H]2C(=O)O[C@H]([C@H](C)C[C@@H]2CC[C@@H](OC(=O)C(C)(CO)CO)[C@H](OC)C2)CC(=O)[C@H](C)/C=C(\C)[C@@H](O)[C@@H](OC)C(=O)[C@H](C)C[C@H](C)/C=C/C=C/C=C/1C
Identifiers
PDB
CAS-ID162635-04-3
RxCUI657797
ChEMBL IDCHEMBL1201182
ChEBI ID79699
PubChem CID6918289
DrugBankDB06287
UNII ID624KN6GM2T (ChemIDplus, GSRS)
Target
Agency Approved
MTOR
MTOR
Organism
Homo sapiens
Gene name
MTOR
Gene synonyms
FRAP, FRAP1, FRAP2, RAFT1, RAPT1
NCBI Gene ID
Protein name
serine/threonine-protein kinase mTOR
Protein synonyms
FK506 binding protein 12-rapamycin associated protein 2, FK506-binding protein 12-rapamycin complex-associated protein 1, FKBP-rapamycin associated protein, FKBP12-rapamycin complex-associated protein, FKBP12-rapamycin complex-associated protein 1, Mammalian target of rapamycin, Mechanistic target of rapamycin, mechanistic target of rapamycin (serine/threonine kinase), mTOR, Rapamycin and FKBP12 target 1, rapamycin associated protein FRAP2, Rapamycin target protein 1
Uniprot ID
Mouse ortholog
Mtor (56717)
serine/threonine-protein kinase mTOR (Q9JLN9)
Alternate
No data
Variants
Clinical Variant
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
Mock data
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Additional graphs summarizing 9,600 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
Mock data
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19,365 adverse events reported
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