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Tenofovir DF in antiretroviral-experienced patients: results from a 48-week, randomized, double-blind study

269

Citations

8

References

2002

Year

Abstract

In treatment-experienced patients with baseline nucleoside resistance mutations, TDF provided dose-related, durable reductions in HIV-1 RNA. Through 24 weeks, the safety profile of TDF was similar to that of placebo.

References

YearCitations

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