Following a public comment period, the USA’s Federal Trade Commission (FTC) has approved a final order settling charges that London-listed Jordanian drugmaker Hikma Pharmaceuticals’ (LSE: HIK) $375 million acquisition of Custopharm likely would have harmed competition in the market for the corticosteroid drug triamcinolone acetonide, or TCA.
Hikma announced the decision to acquire Custopharm - a Californian generic sterile injectables company with a differentiated product portfolio and R&D pipeline - in September 2021, and apart from the upfront payment of $375 million is committed to paying a further $50 million in commercial milestones. At that time, Hikma said it expects addition of the business to generate full year 2021 revenue in excess of $80 million.
Only Custopharm and a few other companies now make this drug. First announced in April 2022, the FTC’s complaint alleged that with this acquisition, Hikma was likely to stop developing its own TCA product, threatening competition in the TCA market.
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