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Gadoteridol
Prohance (gadoteridol) is a small molecule pharmaceutical. Gadoteridol was first approved as Prohance on 1992-11-16.
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Commercial
Therapeutic Areas
No data
Trade Name
FDA
EMA
Prohance, Prohance multipack
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Gadoteridol
Tradename
Company
Number
Date
Products
PROHANCEBracco DiagnosticsN-020131 RX1992-11-16
1 products, RLD, RS
PROHANCE MULTIPACKBracco DiagnosticsN-021489 RX2003-10-09
1 products, RLD, RS
Labels
FDA
EMA
Brand Name
Status
Last Update
prohanceNew Drug Application2022-10-26
Indications
FDA
EMA
No data
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
V: Various drug classes in atc
V08: Contrast media
V08C: Magnetic resonance imaging contrast media
V08CA: Paramagnetic contrast media
V08CA04: Gadoteridol
HCPCS
Code
Description
A9576
Injection, gadoteridol, (prohance multipack), per ml
Clinical
Clinical Trials
13 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
CognitionD003071EFO_000392511
Brain diseasesD001927HP_0001298G93.4011
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Central nervous system diseasesD002493HP_0002011G96.9112
Diagnostic imagingD00395211
Brain neoplasmsD001932EFO_0003833C7111
Indications Phases 2
No data
Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Multiple sclerosisD009103EFO_0003885G35123
GlioblastomaD005909EFO_0000515112
GliomaD005910EFO_000052011
AstrocytomaD001254EFO_000027111
Chronic progressive multiple sclerosisD02052811
Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Central nervous system neoplasmsD01654311
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameGADOTERIDOL
INNgadoteridol
Description
Gadoteridol (INN) is a gadolinium-based MRI contrast agent, used particularly in the imaging of the central nervous system. It is sold under the brand name ProHance. Gadoteridol was first approved for use in the United States in 1992.
Classification
Small molecule
Drug classgadolinium derivatives (principally for diagnostic use)
Image (chem structure or protein)
Structure (InChI/SMILES or Protein Sequence)
CC(O)CN1CCN(CC(=O)[O-])CCN(CC(=O)[O-])CCN(CC(=O)[O-])CC1.[Gd+3]
Identifiers
PDB
CAS-ID120066-54-8
RxCUI25483
ChEMBL IDCHEMBL1200593
ChEBI ID31643
PubChem CID60714
DrugBankDB00597
UNII ID0199MV609F (ChemIDplus, GSRS)
Target
Agency Approved
No data
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 2,018 documents
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Safety
Black-box Warning
Black-box warning for: Prohance
Adverse Events
Top Adverse Reactions
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2,842 adverse events reported
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