Bausch Health picks up US approval for new eye inflammation product

25 February 2019
eye_stock_large-1-

Bausch + Lomb has been granted US Food and Drug Administration approval for Lotemax SM (loteprednol etabonate), a new gel formulation for the treatment of postoperative inflammation and pain following ocular surgery.

Bausch + Lomb is a subsidiary of Bausch Health (TXS: BHC), formerly known as Valeant Pharmaceuticals. The embattled Canadian drugmaker rebranded itself as such in 2018, following its acquisition of the ophthalmic specialist.

Lotemax SM uses SubMicron (SM) technology to adhere to the ocular surface and then penetrate key ocular tissues, helping improve drug exposure into the aqueous humor.

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