California, USA-based biopharmaceutical company Gilead Sciences has received a subpoena from the US Attorney's Office in San Francisco requesting documents regarding its marketing and medical education programs for its HIV drugs Truvada (emtricitabine and tenofovir disoproxil fumarate) and Viread (tenofovir disoproxil fumarate) and Emtriva (emtricitabine).
Gilead says it intends to comply with the Attorney's subpoena and to cooperate in any related government enquiry. The firm's full-year revenues for 2005 were $2.03 billion, up 53% on the previous year and Gilead attributed this success largely to its HIV franchise.
In the first quarter of 2006, sales of those three drugs leapt 50% to $450.7 million. Earlier this year, Gilead signed a deal with US drug major Bristol-Myers Squibb for the development of a product combining the former's Sustiva (efavirenz) with Truvada as a once-daily, single-tablet regimen (Marketletter May 8).
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 2025 | Headless Content Management with Blaze