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Panitumumab information


Panitumumab
Monoclonal antibody
TypeWhole antibody
SourceHuman
TargetEpidermal growth factor receptor (EGFR)
Clinical data
Trade namesVectibix
Other namesABX-EGF
AHFS/Drugs.comMonograph
MedlinePlusa607066
License data
  • EU EMA: by INN
  • US DailyMed: Panitumumab
Routes of
administration
Intravenous
ATC code
  • L01FE02 (WHO)
Legal status
Legal status
  • US: WARNING[1]Rx-only[2]
  • EU: Rx-only[3]
  • In general: ℞ (Prescription only)
Pharmacokinetic data
Elimination half-life~9.4 days (range: 4-11 days)
Identifiers
CAS Number
  • 339177-26-3 checkY
DrugBank
  • DB01269 checkY
ChemSpider
  • none
UNII
  • 6A901E312A
KEGG
  • D05350
ChEMBL
  • ChEMBL1201827 ☒N
PDB ligand
  • 5sx4 (PDBe, RCSB PDB)
Chemical and physical data
FormulaC6398H9878N1694O2016S48
Molar mass144324.12 g·mol−1
 ☒NcheckY (what is this?)  (verify)

Panitumumab, sold under the brand name Vectibix, is a fully human monoclonal antibody specific to the epidermal growth factor receptor (also known as EGF receptor, EGFR, ErbB-1 and HER1 in humans).[2][3]

Panitumumab is manufactured by Amgen and was originally developed by Abgenix Inc.

In 2014, Amgen and Illumina entered into an agreement to develop a companion diagnostic to accompany panitumumab.[4]

  1. ^ "FDA-sourced list of all drugs with black box warnings (Use Download Full Results and View Query links.)". nctr-crs.fda.gov. FDA. Retrieved 22 Oct 2023.
  2. ^ a b "Vectibix- panitumumab solution". DailyMed. 25 August 2021. Archived from the original on 6 April 2022. Retrieved 6 July 2022.
  3. ^ a b "Vectibix EPAR". European Medicines Agency. 17 September 2018. Archived from the original on 13 August 2021. Retrieved 6 July 2022.
  4. ^ "Illumina, Amgen to Develop CDx for Colorectal Cancer". News: Molecular Diagnostics. Gen. Eng. Biotechnol. News (paper). Vol. 34, no. 4. February 15, 2014. p. 32. Archived from the original on September 19, 2016. Retrieved December 2, 2014.

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