Truvada (TDF/FTC)

Antiretroviralprescriptionoral · inferred

Fixed-dose combination of tenofovir disoproxil fumarate 300 mg and emtricitabine 200 mg. Backbone of HIV treatment regimens and the original FDA-approved HIV PrEP (2012). One pill once daily with or without food. Dose-limiting PK is tenofovir's plasma half-life (~17h) and intracellular TFV-DP half-life (~50h). See component entries for full PK of each moiety.

Projected serum levels — 1 pill (≈ 500 mg), once daily

Truvada (TDF/FTC)
Truvada (TDF/FTC) modeled serum levels, 1 pill (≈ 500 mg) once daily over 15 days Population-based pharmacokinetic estimate. Steady state reached after approximately 1 days. 0 50 100 150 200 Day 0 Day 4 Day 8 Day 11 Day 15 Time on a regular schedule ≈ steady state · day 1

Maintenance schedule: 1 pill (≈ 500 mg) once daily (oral).

Modeled steady state after ~1 days: peak ≈ 189 mg, trough ≈ 9.7 mg body load. Population-based estimate over 15 days for a reference dose at a 70 kg reference body mass — the interactive app scales curves to your doses, timing, and body mass.

Key facts

Category
Antiretroviral
Route modeled
Oral
Model confidence
inferred
Half-life
4.9 h
Common dose
1 pill (≈ 500 mg)
Suggested maximum
1 pill/day
Reference dose range
0.50–1 pill (single dose)
Suggested cadence
once daily

Research behind this entry

  1. Preexposure chemoprophylaxis for HIV prevention in men who have sex with men Grant RM et al. · New England Journal of Medicine, 2010 DOI

    Landmark iPrEx trial establishing daily oral TDF/FTC as effective HIV pre-exposure prophylaxis, with 44% overall reduction and >90% in adherent participants.

  2. Antiretroviral preexposure prophylaxis for heterosexual HIV transmission in Botswana Thigpen MC et al. · New England Journal of Medicine, 2012 DOI

    TDF2 study confirming TDF/FTC PrEP efficacy (62% reduction) in heterosexual men and women, broadening clinical applicability.

2 published studies referenced in the app, each with a plain-language summary.