Bristol-Myers continues multiple myeloma trials after FDA lifts partial holds

6 December 2017
2019_biotech_test_vial_discovery_big

Three months after the US FDA put a partial hold on three clinical trials investigating Opdivo (nivolumab) combinations in multiple myeloma, the agency has given Bristol-Myers Squibb (NYSE: BMY) and its collaborators the all clear to continue two of the studies.

The holds were placed on the Phase I CA209039 (CheckMate-039) and the Phase II CA204142 studies after risks were identified in three other multiple myeloma trials of rival PD-1 agent Keytruda (pembrolizumab).

Safety monitors in those studies reported a higher incidence of death among those receiving Keytruda.

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