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Drug ReportsCustirsen
Custirsen
Custirsen is an oligonucleotide pharmaceutical. It is currently being investigated in clinical studies.
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Commercial
Clinical
Drug
Target
Variants
Financial
Trends
Safety
Events Timeline
5D
1M
3M
6M
YTD
1Y
2Y
5Y
Max
Events
FDA approval date
EMA approval date
Patent expiration date
Study first post date
Last update post date
Start date
Primary completion date
Completion date
Results first post date
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Commercial
No data
Clinical
Clinical Trials
13 clinical trials
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Indications Phases 4
No data
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Prostatic neoplasmsD011471—C61233——8
Lung neoplasmsD008175HP_0100526C34.90211——3
Non-small-cell lung carcinomaD002289——111——2
Castration-resistant prostatic neoplasmsD064129————1——1
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Breast neoplasmsD001943EFO_0003869C5011———2
Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
NeoplasmsD009369—C802————2
Ovarian neoplasmsD010051EFO_0003893C561————1
Urinary bladder neoplasmsD001749—C671————1
Kidney neoplasmsD007680EFO_0003865C641————1
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameCustirsen
INNcustirsen
Description
Custirsen, with aliases including custirsen sodium, OGX-011, and CC-8490, is an investigational drug that is under clinical testing for the treatment of cancer. It is an antisense oligonucleotide (ASO) targeting clusterin expression. In metastatic prostate cancer, custirsen showed no benefit in improving overall survival.
Classification
Oligonucleotide
Drug classantisense oligonucleotides
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Structure (InChI/SMILES or Protein Sequence)—
Identifiers
PDB—
CAS-ID890056-27-6
RxCUI—
ChEMBL IDCHEMBL2108309
ChEBI ID—
PubChem CID—
DrugBankDB05487
UNII IDL26E95NLRK (ChemIDplus, GSRS)
Target
No data
Variants
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 241 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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29 adverse events reported
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