| Literature DB >> 31497242 |
Abstract
With the scale-up of HIV pre-exposure prophylaxis (PrEP) with tenofovir (TDF) with or without emtricitabine (FTC), we have entered an era of highly effective HIV prevention with a growing pipeline of potential products to be studied. These studies are likely to be randomized trials with an oral TDF/FTC control arm. These studies require comparison of incident infections and can be time and resource intensive. Conventional approaches for design and analysis active controlled trial can lead to very large sample sizes. We demonstrate the important of assumptions about background infections for interpreting trial results and suggest alternative criteria for demonstrating the efficacy and effectiveness of potential PrEP agents.Entities:
Keywords: active controlled; hiv prevention; non-inferiority; pre-exposure prophylaxis
Year: 2019 PMID: 31497242 PMCID: PMC6731035 DOI: 10.1515/scid-2019-0011
Source DB: PubMed Journal: Stat Commun Infect Dis