Vectibix

panitumumab · Amgen Europe B.V.
AUTHORISED IN THE EU

What Vectibix is used for

Vectibix is indicated for the treatment of adult patients with wild-type RAS metastatic colorectal cancer (mCRC): in first-line in combination with Folfox or Folfiri. in second-line in combination with Folfiri for patients who have received first-line fluoropyrimidine-based chemotherapy (excluding irinotecan). as monotherapy after failure of fluoropyrimidine-, oxaliplatin-, and irinotecan-containing chemotherapy regimens.

Approved use, as published by the European Medicines Agency.

Key facts

Brand
Vectibix
Active substance
panitumumab
Disease area
Colorectal Neoplasms
Medicine group
Antineoplastic agents
ATC code
L01XC08
Marketing authorisation holder
Amgen Europe B.V.
Authorised in the EU since
2007

Official information

In the USA

Same active substance: Vectibix

In India

Specialist medicine: started and supervised by a specialist doctor or hospital. This page is a plain-language summary of public official information, not medical advice; follow your doctor and the official product information.

Common questions

What is Vectibix used for?

Vectibix is indicated for the treatment of adult patients with wild-type RAS metastatic colorectal cancer (mCRC): in first-line in combination with Folfox or Folfiri. in second-line in combination with Folfiri for patients who have received first-line fluoropyrimidine-based chemotherapy (excluding irinotecan). as monotherapy after failure of fluoropyrimidine-, oxaliplatin-, and irinotecan-containing chemotherapy regimens.

What is the active substance in Vectibix?

Vectibix contains panitumumab.

Who makes Vectibix?

The EU marketing authorisation holder is Amgen Europe B.V..

Source: European Medicines Agency medicines data (ema.europa.eu), reproduced with acknowledgement of the source. Page made 5 November 2026 by Satya Babu.

← All specialty medicines, EU

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