US pharma major Eli Lilly (NYSE: LLY) says it is delaying the submission of its basal insulin peglispro (BIL) to regulatory agencies beyond the first quarter of 2015.
The delay includes filings with the US Food and Drug Administration and the European Medicines Agency. Analysts had expected Lilly's drug to reach sales of about $242 million by 2018, according to Thomson Reuters data. If approved, it would compete directly with French pharma major Sanofi’s (Euronext: SAN) Lantus (insulin glargine), which generated 2014 sales of 6.34 billion euros ($7.2 billion).
Delay is to generate additional clinical data
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