US pharma major AbbVie (NYSE: ABBV) has recently submitted a supplementary new drug application (sNDA) to the US Food and Drug Administration for Vraylar (cariprazine) as the adjunctive treatment of major depressive disorder (MDD).
However, pricey Vraylar will have to compete with low-cost aripiprazole and quetiapine generics, with competition becoming even fiercer when generic brexpiprazole enters the market in 2026, according to data and analytics company GlobalData.
Vraylar is already an FDA-approved product to treat adults with depressive, acute manic and mixed episodes associated with bipolar I disorder, as well as schizophrenia.
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