First tumor-agnostic nod for Tafinlar plus Mekinist in the USA

23 June 2022
novartis_logo_big

Swiss pharma giant Novartis (NOVN: VX) has received an Accelerated Approval in the USA for its combination BRAF/MEK inhibitor therapy, for certain biomarker-defined tumors.

The nod makes the Tafinlar (dabrafenib) plus Mekinist (trametinib) treatment the first and only therapy of its kind available in a tumor-agnostic indication, for solid tumors carrying the BRAF V600E mutation.

This mutation is known to drive tumor growth in more than 20 different types of cancer, and the decision from the US Food and Drug Administration will bring a new treatment option for people with no alternatives.

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

Companies featured in this story

More ones to watch >


Today's issue

Company Spotlight





More Features in Biotechnology