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Drug ReportsEFAVALEUKIN ALFA
EFAVALEUKIN ALFA
Efavaleukin alfa is a protein 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
9 clinical trials
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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
Graft vs host diseaseD006086D89.81313
Bronchiolitis obliterans syndromeD000092122313
Systemic lupus erythematosusD008180HP_0002725M32112
Ulcerative colitisD003093EFO_0000729K5122
ColitisD003092EFO_0003872K52.922
UlcerD014456MPATH_57922
Rheumatoid arthritisD001172EFO_0000685M06.9111
ArthritisD001168HP_0001369M05-M14111
Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
MyositisD009220EFO_0000783G72.4911
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameEFAVALEUKIN ALFA
INNefavaleukin alfa
Description
Efavaleukin alfa is an experimental drug that works as an interleukin-2 "mutein Fc fusion protein that preferentially binds the high-affinity IL-2 receptor alpha chain (CD25) to selectively promote Treg expansion". It is developed to treat systemic lupus erythematosus (SLE).
Classification
Protein
Drug classFc fusion protein; interleukins: interleukin-2 analogues and derivatives
Image (chem structure or protein)Loading
Structure (InChI/SMILES or Protein Sequence)
Identifiers
PDB
CAS-ID
RxCUI
ChEMBL IDCHEMBL4298204
ChEBI ID
PubChem CID
DrugBank
UNII IDYNH9K62UXU (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 21 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
0 adverse events reported
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