Vismed enters US trial for dry eye syndrome

22 January 2007

USA-based drug development firm Lantibio and Swiss pharmaceutical company TRB Chemedica have initiated a Phase III clinical trial of the drug Vismed, a patented formulation of sodium hyaluronate, as a treatment for dry eye syndrome. The study is being carried out under Special Protocol Assessment criteria as dictated by the Food and Drug Administration.

The drug, which is already available in Europe, is being studied in the USA under Investigational New Drug application number 73,441, filed in June last year. If the current program is successful, the firms expect to file a New Drug Application with the FDA in 2008.

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