darunavir receives us fda approval

Inpharma 1662 - 1 Nov 2008 ■ Darunavir receives US FDA approval. Tibotec Therapeutics has announced that darunavir [Prezista] has received US FDA approval for an expanded indication for once-daily dosing as part of HIV combination therapy in treatment-naive adults. The FDA also granted full approval to darunavir as twice- daily for use in treatment-experienced adult patients. Tibotec Therapeutics. U.S. Food and Drug Administration (FDA) Approves PREZISTA(R) Once-Daily as Part of Combination Therapy for Treatment- Naive Adults with HIV-1. Media Release : 22 Oct 2008. Available from: URL: http://www.tibotec.com 809094302 1 Inpharma 1 Nov 2008 No. 1662 1173-8324/10/1662-0001/$14.95 Adis © 2010 Springer International Publishing AG. All rights reserved

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Page 1: Darunavir receives US FDA approval

Inpharma 1662 - 1 Nov 2008

■ Darunavir receives US FDA approval. TibotecTherapeutics has announced that darunavir [Prezista]has received US FDA approval for an expandedindication for once-daily dosing as part of HIVcombination therapy in treatment-naive adults. TheFDA also granted full approval to darunavir as twice-daily for use in treatment-experienced adult patients.Tibotec Therapeutics. U.S. Food and Drug Administration (FDA) ApprovesPREZISTA(R) Once-Daily as Part of Combination Therapy for Treatment-Naive Adults with HIV-1. Media Release : 22 Oct 2008. Available from:URL: http://www.tibotec.com 809094302

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