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Elcubragistat
Elcubragistat is a small molecule pharmaceutical. It is currently being investigated in clinical studies.
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Commercial
Therapeutic Areas
No data
Trade Name
FDA
EMA
No data
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
No data
Labels
FDA
EMA
No data
Indications
FDA
EMA
No data
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
No data
HCPCS
No data
Clinical
Clinical Trials
6 clinical trials
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Mock data
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Indications Phases 4
No data
Indications Phases 3
No data
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Tic disordersD013981F95112
Tourette syndromeD005879EFO_0004895F95.2112
Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
PainD010146EFO_0003843R5211
Diabetic neuropathiesD003929EFO_100078311
Postherpetic neuralgiaD05147411
Small fiber neuropathyD00007107511
Multiple sclerosisD009103EFO_0003885G3511
Neuromyelitis opticaD009471EFO_0004256G36.011
Transverse myelitisD009188G37.311
MyelitisD009187G04.9111
DyspepsiaD004415EFO_0008533K3011
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameELCUBRAGISTAT
INNelcubragistat
Description
Elcubragistat is a small molecule pharmaceutical. It is currently being investigated in clinical studies.
Classification
Small molecule
Drug classenzyme inhibitors
Image (chem structure or protein)
Structure (InChI/SMILES or Protein Sequence)
O=C(OC(C(F)(F)F)C(F)(F)F)N1CCN(Cc2ccc(C(F)(F)F)cc2N2CCCC2)CC1
Identifiers
PDB
CAS-ID1446817-84-0
RxCUI
ChEMBL IDCHEMBL3945728
ChEBI ID
PubChem CID
DrugBank
UNII IDFB39E94UXK (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:
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Additional graphs summarizing 0 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
0 adverse events reported
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