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Boehringer Ingelheim Pharmaceuticals announced that the FDA has granted full approval of Aptivus (tipranavir) capsules. The full approval of Aptivus based largely on 48-week analyses of the Phase III pivotal clinical studies known as the RESIST (Randomized Evaluation of Strategic Intervention in Multi-Drug ReSistant Patients with Tipranavir) trials. These trials comprise one of the largest study programs conducted in treatment-experienced HIV patients. The FDA granted accelerated approval to Aptivus in June 2005. Accelerated approval is a regulatory process that expedites the approval of therapies for serious or life-threatening illnesses.

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