The benefits of using Nuplazid (pimavanserin) for psychosis associated with Parkinson’s disease outweigh the risks, according to a vote of the US Food and Drug Administration (FDA) Psychopharmacologic Drugs Advisory Committee.
There were 12 votes in favor and two against the use of the medication, for which US company Acadia Pharmaceuticals (Nasdaq: ACAD) has submitted a new drug application (NDA).
The regulator has granted Nuplazid priority status for its review of the NDA, which has to be completed by May 1 this year.
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