Due to poor results from a Phase IIa study of Topiagen Pharmaceuticals' TPI 1020 in chronic obstructive pulmonary disease, the US drugmaker has decided to discontinue the agent in this indication.
TPI 1020 showed good overall safety and tolerability, although its activity profile was not significantly different from budesonide, a common corticosteroid used in respiratory disorders. The agent is a New Chemical Entity licensed from French firm NicOx SA for respiratory indications.
In light of the poor efficacy results, Topigen and NicOx have decided to discontinue the development of TPI 1020 in COPD and will explore potential opportunities for this compound in other indications.
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 accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
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
| Headless Content Management with Blaze