USA-based Tranzyme Pharma (Nasdaq: TZYM) and independent drugmaker Norgine of the Netherlands yesterday announced top-line results of the primary analysis of ULISES 007, the first of two Phase III pivotal trials evaluating its bowel cancer drug candidate ulimorelin, noting that it failed to meet its primary and secondary efficacy endpoints.
The news saw Tranzyme’s shares plummet nearly 70% to $1.55 in pre-market trading on Monday. Prior to this fall, the company had a market capitalization of just over $125 million, noted a Reuters report.
"These results are surprising and disappointing. While we are still planning to analyze the data from the second Phase III trial ULISES 008, which we expect by the end of the second quarter, we are stopping all other NDA [New Drug Application] activities for ulimorelin," said Vipin Garg, president and chief executive of Tranzyme Pharma.
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
Copyright © The Pharma Letter 2024 | Headless Content Management with Blaze