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Futuximab

From Wikipedia, the free encyclopedia
Monoclonal antibody
Pharmaceutical compound
Futuximab
Monoclonal antibody
TypeWhole antibody
SourceChimeric (mouse/human)
TargetHER1
Clinical data
Other names992 DS
ATC code
  • none
Identifiers
CAS Number
ChemSpider
  • none
UNII
Chemical and physical data
FormulaC6468H10002N1724O2055S46
Molar mass146269.94 g·mol−1

Futuximab (992 DS) (INN) is a chimeric monoclonal antibody designed for the treatment of cancer.[1] It acts as animmunomodulator and also binds toHER1.[2][3]

This drug was developed bySymphogen.

References

[edit]
  1. ^Statement On A Nonproprietary Name Adopted By The USAN Council - Futuximab,American Medical Association.
  2. ^World Health Organization (2012)."International Nonproprietary Names for Pharmaceutical Substances (INN). Proposed INN: List 107"(PDF).WHO Drug Information.26 (2).
  3. ^Keir ST, Chandramohan V, Hemphill CD, Grandal MM, Melander MC, Pedersen MW, Horak ID, Kragh M, Desjardins A, Friedman HS, Bigner DD (July 2018)."Sym004-induced EGFR elimination is associated with profound anti-tumor activity in EGFRvIII patient-derived glioblastoma models".J. Neurooncol.138 (3):489–498.doi:10.1007/s11060-018-2832-6.PMC 5999169.PMID 29564747.
Tumor
Human
Mouse
Chimeric
Humanized
Rat/mouse hybrid
Chimeric + humanized
Angiopoietin
CNTF
EGF (ErbB)
EGF
(ErbB1/HER1)
ErbB2/HER2
ErbB3/HER3
ErbB4/HER4
FGF
FGFR1
FGFR2
FGFR3
FGFR4
Unsorted
HGF (c-Met)
IGF
IGF-1
IGF-2
Others
LNGF (p75NTR)
PDGF
RET (GFL)
GFRα1
GFRα2
GFRα3
GFRα4
Unsorted
SCF (c-Kit)
TGFβ
Trk
TrkA
TrkB
TrkC
VEGF
Others


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