Fast nonlinear mixed effects (NLME) modeling in R, powered by a Rust backend with Enzyme automatic differentiation for exact gradients.
- FOCE/FOCEI estimation with automatic differentiation
- Analytical PK models: 1- and 2-compartment (oral/IV)
- ODE-based models: Dormand-Prince RK45 solver for general ODEs
- NONMEM-compatible: reads standard NONMEM CSV datasets
- BLOQ handling: Beal's M3 likelihood for observations below the LLOQ
- Model DSL: define models in
.ferxtext files
A Rust installation with the Enzyme AutoDifferentiation engine is required for FeRx to compute gradients. Most likely you will need to build Rust from source, which may take an hour or so.
See documentation for installation instructions.
After installing Rust, in R run:
devtools::install_github("InsightRX/ferx")Or from a local clone:
R CMD INSTALL .A Docker image is available that bundles the Enzyme toolchain (built from source), ferx CLI, the ferx R package, and RStudio Server — no local Rust/Enzyme setup required. If you're on Windows, this is currently the only supported way of running FeRx.
# Build (first build takes ~45-60 min; cached after that)
docker build -t ferx:latest .
# Run RStudio Server
docker run --rm -p 8787:8787 -e PASSWORD=ferx ferx:latest
# -> http://localhost:8787 user: rstudio password: ferxlibrary(ferx)
# Get bundled example paths
ex <- ferx_example("warfarin")
# Fit a one-compartment oral PK model
result <- ferx_fit(ex$model, ex$data, method = "focei")
result
# Simulate at the fitted estimates (typical VPC flow)
sim <- ferx_simulate(ex$model, ex$data, n_sim = 100, seed = 42, fit = result)
# Population predictions at the fitted estimates
preds <- ferx_predict(ex$model, ex$data, fit = result)Pass fit = <ferx_fit result> to ferx_simulate() / ferx_predict() to use
the fitted theta / omega / sigma. Omit it to use the model file's initial
values.
For observations below the lower limit of quantification, flag them with a
CENS column in the data (1 = censored, with DV carrying the LLOQ value)
and pass bloq_method = "m3" to ferx_fit(). Each censored observation then
contributes P(y < LLOQ | θ, η) = Φ((LLOQ − f)/√V) to the likelihood instead
of a Gaussian residual, avoiding the terminal-phase bias that comes from
simply dropping BLOQ rows.
bloq <- ferx_example("warfarin_bloq")
result <- ferx_fit(bloq$model, bloq$data, method = "focei", bloq_method = "m3")
sim <- ferx_simulate(bloq$model, bloq$data, n_sim = 100, seed = 42, fit = result)See inst/examples/ex1a_warfarin_bloq.R for a full fit + VPC walkthrough.
Models are defined in .ferx files:
[parameters]
theta TVCL(0.2, 0.001, 10.0) # name(initial, lower, upper)
theta TVV(10.0, 0.1, 500.0)
theta TVKA(1.5, 0.01, 50.0)
omega ETA_CL ~ 0.09 # between-subject variability (variance)
omega ETA_V ~ 0.04
omega ETA_KA ~ 0.30
sigma PROP_ERR ~ 0.02
[individual_parameters]
CL = TVCL * exp(ETA_CL)
V = TVV * exp(ETA_V)
KA = TVKA * exp(ETA_KA)
[structural_model]
pk one_cpt_oral(cl=CL, v=V, ka=KA)
[error_model]
DV ~ proportional(PROP_ERR)
See ferx_example() for available bundled examples.
| Function | Description |
|---|---|
ferx_fit() |
Fit a NLME model (FOCE/FOCEI). bloq_method = "m3" enables M3. |
ferx_simulate() |
Simulate replicates with BSV and residual error. Pass fit = to use fitted estimates. |
ferx_predict() |
Population predictions (ETA = 0). Pass fit = to use fitted theta. |
ferx_example() |
Get paths to bundled example models and data |
MIT — see LICENSE.md.
Copyright © 2026 InsightRX, Inc.