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Those are two different kinds of evidence, and neither establishes that one route produces greater systemic exposure in a living organism
Scientific Values
Pipeline highlights In HIV, Gilead submitted a new drug application (NDA) with FDA and a marketing authorization application (MAA) with the European Medicines Agency (EMA) for Biktarvy, a once-daily single tablet regimen containing bictegravir, a novel investigational integrase strand transfer inhibitor, emtricitabine and tenofovir alafenamide (TAF) for the treatment of HIV infection in adults
On the back of phase II trials, its already being hailed as a game-changer
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