Japan-based Dainippon Sumitomo Pharma presented positive results from the first Phase III trial of lurasidone, which is under clinical development globally, for the treatment of patients with schizophrenia, at the meeting of the American Psychiatric Association, held in San Francisco, California.
The randomized, placebo-controlled, double-blind trial evaluated the efficacy and safety of lurasidone 40mg, 80mg and 120mg once daily compared to placebo, over six weeks in patients with acute schizophrenia. The 80mg/day dose was significantly more effective than placebo during the study.
Lurasidone was also well tolerated with a lower overall discontinuation rate (31%) compared to placebo (43%) and few adverse event-related discontinuations (6% and 2% for lurasidone and control, respectively).
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 2025 | Headless Content Management with Blaze