Understanding the therapeutic value of cancer drugs after initial FDA approval

23 June 2015

The full therapeutic value of a cancer therapy is typically realized long after the drug's initial Food and Drug Administration approval, according to a report from Boston Healthcare.

In the report, several industry examples demonstrate why FDA approval should be viewed as a starting point for additional research into a drug's full therapeutic potential.

The Value of Innovation in Oncology: Recognizing Emerging Benefits Over Time was commissioned by the Pharmaceutical Research and Manufacturers of America (PhRMA) and examines the pathways by which additional benefits of cancer therapies are revealed over time through continuing research after initial FDA approval.

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 Pharmaceutical