US firm Optimer Pharmaceuticals, a specialist developer of carbohydrate-based anti-infectives, has reported positive results from the second of two double-blind pivotal Phase III trials assessing the safety and efficacy of prulifloxacin (600mg) as a once-daily, three-day oral therapy for the treatment of infectious diarrhea.
Prulifloxacin showed a statistically-significant benefit compared to placebo in Time to Last Unformed Stool (TLUS) in both the intent-to-treat (n=200) and microbiologically-evaluable (n=173) populations. The median TLUS for patients treated with prulifloxacin was 32.8 hours; this was significant versus placebo (p<0.0001).
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