Nycomed's Teslascan Gets EU Clearance

11 June 1997

Nycomed of Norway has been granted centralized European Union approvalfor the company's first organ-specific contrast agent, Teslascan (mangafodipir) for use in magnetic resonance imaging. The company has also been issued with an approvable letter for the product from the US Food and Drug Administration.

Teslascan is used for the diagnosis of liver disease, and will enable MRI to be used as a substitute or follow-up for computed tomography, the imaging technique most often used for liver conditions. Nycomed Imaging plans to start marketing Teslascan in the EU during the third quarter of 1997, and says it expects to gain considerable market share in this relatively specific sector.

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