Precision lung cancer med submitted for US approval

4 December 2020
janssen_johnson_big

The pharmaceutical arm of Johnson & Johnson (NYSE: JNJ) has submitted to the US regulator for approval to market amivantamab in non-small cell lung cancer (NSCLC).

The bispecific antibody targets tumors with EGFR and MET mutations, and the firm is seeking a green light to offer the product for people with metastatic lung cancers of this type.

If approved, the therapy would be the first available treatment which specifically targets NSCLC with this kind of genetic mutation.

This article is accessible to registered users, to continue reading please register for free.  A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.

Login to your account

Become a subscriber

 

£820

Or £77 per month

Subscribe Now
  • Unfettered access to industry-leading news, commentary and analysis in pharma and biotech.
  • Updates from clinical trials, conferences, M&A, licensing, financing, regulation, patents & legal, executive appointments, commercial strategy and financial results.
  • Daily roundup of key events in pharma and biotech.
  • Monthly in-depth briefings on Boardroom appointments and M&A news.
  • Choose from a cost-effective annual package or a flexible monthly subscription
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed

Chairman, Sanofi Aventis UK

Today's issue

Company Spotlight





More Features in Biotechnology