AMO Pharma and Ranedis target rare genetic diseases in RND-001 deal

14 March 2017
amo_pharma_large

Privately-held companies AMO Pharma and Ranedis Pharmaceuticals have announced a collaboration to progress the development of RND-001 for rare genetic diseases, including certain lysosomal storage disorders and other diseases affecting the central nervous system.

As part of the deal, financial terms of which were not disclosed, Ranedis has granted AMO an exclusive option to acquire the worldwide rights to RND-001 during the collaboration period.

"RND-001 reflects the qualities we look for in asset acquisition, such as strong scientific rationale and opportunity to address unmet needs in rare diseases"

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