Necitumumab

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Necitumumab
Necitumumab EGFR 6B3S.png
Necitumumab Fab (blue) bound to EGFR (green). PDB: 6B3S
Monoclonal antibody
Type Whole antibody
Source Human
Target EGFR
Clinical data
Trade names Portrazza
AHFS/Drugs.com Multum Consumer Information
License data
Routes of
administration
Intravenous infusion
ATC code
Legal status
Legal status
Pharmacokinetic data
Elimination half-life ~14 days
Identifiers
CAS Number
DrugBank
ChemSpider
  • none
UNII
KEGG
Chemical and physical data
Formula C6436H9958N1702O2020S42
Molar mass 144844.87 g·mol−1
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Necitumumab (INN) is a recombinant human IgG1 monoclonal antibody used as an antineoplastic, which is manufactured by Eli Lilly. It binds to the epidermal growth factor receptor (EGFR). [2] The US FDA approved necitumumab under the brand name Portrazza for use with gemcitabine and cisplatin in previously untreated metastatic squamous non-small-cell lung carcinoma (NSCLC). [3] [4] [5] It was counterproductive in non-squamous non-small-cell lung carcinoma. [5] [6]

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References

  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. International Nonproprietary Names for Pharmaceutical Substances (INN, prepublication copy), World Health Organization.
  3. Chustecka Z (2015-11-22). "Necitumumab (Portrazza) Approved for Lung Cancer in US". Medscape.com. Retrieved 2019-09-28.
  4. "Necitumumab". Approved Drugs. U.S. Food and Drug Administration. Archived from the original on 2017-01-11. Retrieved 2019-12-16.
  5. 1 2 "Portrazza: Highlights of Prescribing Information" (PDF). www.accessdata.fda.gov. 2015. Retrieved 2019-09-28.
  6. Hand L (3 March 2015). "Necitumumab Fails in NSCLC". MedScape. Archived from the original on 2015-11-29. Retrieved 2015-11-25.