J&J files in Europe for subcutaneous Darzalex formulation

19 July 2019
jnjn_flickr_big

Johnson & Johnson’s (NYSE: JNJ) pharma business Janssen has submitted for approval to broaden the European label for Darzalex (daratumumab), for subcutaneous treatment of multiple myeloma.

The product is co-formulated with recombinant human hyaluronidase PH20 (rHuPH20), an approach developed by US-based biotech Halozyme Therapeutics (Nasdaq: HALO).

Halozyme has found high demand for its drug delivery technology, with big pharma clients including Roche (ROG: SIX), AbbVie (NYSE: ABBV), Bristol-Myers Squibb (NYSE: BMY) and Eli Lilly (NYSE: LLY).

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

Company News Directory



Companies featured in this story

More ones to watch >




Today's issue

Company Spotlight



More Features in Biotechnology