ABP 710: Withdrawal of the marketing authorisation application

infliximab

Overview

Amgen Europe B.V. withdrew its application for a marketing authorisation of ABP 710 for the treatment of inflammatory diseases.

The company withdrew the application on 27 May 2019.

Key facts

Name
ABP 710
Product number
EMEA/H/C/005020
International non-proprietary name (INN) or common name
  • infliximab
Active substance
  • infliximab
Date of withdrawal
27/05/2019
Company making the application
Amgen Europe B.V.
Withdrawal type
Initial authorisation

Related information on withdrawals

A question-and-answer (Q&A) document provides a summary of the CHMP's evaluation of the medicine at the time of the withdrawal of the application, and includes a link to the company's formal withdrawal letter (withdrawal letter Doc. type, leave the 'Author' in properties blank).

An assessment report is published when the application is withdrawn after the first stage of the CHMP's evaluation is completed ('day 120').

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