Adjuvant Opdivo shows superiority to Yervoy in resected high-risk melanoma

5 July 2017
2019_biotech_test_vial_discovery_big

US pharma major Bristol-Myers Squibb (NYSE: BMY) has announced results from a Phase III study comparing Opdivo (nivolumab) to Yervoy (ipilimumab) in stage IIIb/c or stage IV melanoma who are at high risk of recurrence following complete surgical resection.

The CheckMate -238 trial met its primary endpoint at a planned interim analysis, demonstrating superior recurrence-free survival (RFS) in patients receiving Opdivo compared to Yervoy.

Both drugs belong to B-MS, where Vicki Goodman is development lead for melanoma and genitourinary cancers.

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