Paion provides update on clinical and commercial activities

14 August 2017
2019_biotech_test_vial_discovery_big

German drug developer Paion (FSE: PA8) has provided a clinical and commercial update of its activities, indicating that lead candidate remimazolam will now likely be filed for regulatory approval in the USA in the second half of next year, later than had previously been expected.

The review was carried out on the company’s behalf by Edison Investment Research.

To support a potential US filing, the company is undertaking additional Phase I studies to assess whether the drug could be abused intranasally and whether it could be used as a knock-out cocktail in combination with alcohol.

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





More Features in Biotechnology