The US regulator has issued a warning to AcelRx Pharmaceuticals (Nasdaq: ACRX) over its marketing of opioid analgesic Dsuvia (sufentanil), causing shares in the company to fall 8%.
The sublingual tablet, which is approved for the management of acute pain in adults, is used when people are not able to receive treatment orally or through intravenous injection.
The US Food and Drug Administration said that AcelRx had “disseminated promotional communications that undermine key prescribing conditions required for the safe use” of the product.
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