U.S. Food And Drug Administration Approves Labeling Update For PREZISTA(R) To Include 96-Week Data In HIV-1 Infected Adult Patients

Tibotec Therapeutics announced that the U.S. Food and Administration (FDA) has approved a labeling update for PREZISTA® (darunavir) tablets to include 96-week data from the ARTEMIS and TITAN studies. Both ARTEMIS and TITAN evaluated the efficacy and safety of PREZISTA with ritonavir (r) vs…


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