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Ramucirumab information


Ramucirumab
Monoclonal antibody
TypeWhole antibody
SourceHuman
TargetVEGFR2 (KDR)
Clinical data
Trade namesCyramza
Other namesLY3009806, IMC-1121B
AHFS/Drugs.comcyramza
Routes of
administration
Intravenous infusion
ATC code
  • L01FG02 (WHO)
Legal status
Legal status
  • AU: S4 (Prescription only)[1]
  • CA: ℞-only[2]
  • US: ℞-only
Pharmacokinetic data
MetabolismProbably proteases
Elimination half-life14 days
Identifiers
CAS Number
  • 947687-13-0 ☒N
DrugBank
  • DB05578 checkY
ChemSpider
  • none
UNII
  • D99YVK4L0X
Chemical and physical data
FormulaC6374H9864N1692O1996S46
Molar mass143609.63 g·mol−1
 ☒NcheckY (what is this?)  (verify)

Ramucirumab[3] (brand name Cyramza[4][5]) is a fully human monoclonal antibody (IgG1) developed for the treatment of solid tumors. This drug was developed by ImClone Systems Inc. It was isolated from a native phage display library from Dyax.

  1. ^ "Prescription medicines: registration of new chemical entities in Australia, 2015". Therapeutic Goods Administration (TGA). 21 June 2022. Retrieved 10 April 2023.
  2. ^ "Health Canada New Drug Authorizations: 2015 Highlights". Health Canada. 4 May 2016. Retrieved 7 April 2024.
  3. ^ Statement On A Nonproprietary Name Adopted By The USAN Council - Ramucirumab, American Medical Association.
  4. ^ "FDA OKs Lilly's blockbuster hopeful ramucirumab for stomach cancer". FierceBiotech. 21 April 2014.
  5. ^ "Cyramza official website".

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