Pediatric bevacizumab minimal PBPK
Reference paper ↗A minimal PBPK model connecting body-weight-scaled bevacizumab clearance and compartment volumes to central and peripheral antibody exposure.
- Therapeutic
- Bevacizumab
- Modality
- Monoclonal antibody
- Target
- VEGF-A
- Disease
- Pediatric-to-adult bevacizumab exposure bridging
- Model type
- PBPK
Complete model workspace
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- Parameters
- 6
- States
- 3
- Equations
- 3
- Derived outputs
- 11
Explore this model
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Female >=18 10 mg/kg every 2 weeks
How does pediatric body weight change bevacizumab compartment volumes, clearance, concentration, and exposure? Explore this intervention regimen through Central bevacizumab concentration, Cumulative bevacizumab exposure, Total bevacizumab clearance, Central distribution volume.
Starting result
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Starting configuration
Time: 0–3,024 hour; step 4
| Input | Default | Available range |
|---|---|---|
| Body weight | 62 kg | 31–93 kg |
| Catabolic clearance | 0.0175 L/h | 0.00875–0.02625 L/h |
| Additional clearance | 0.00278 L/h | 0.00139–0.00417 L/h |
| Central volume | 0.03812 L/kg | 0.01906–0.05718 L/kg |
| Peripheral volume | 0.02859 L/kg | 0.01429–0.04288 L/kg |
Expected readouts
Central bevacizumab concentration · Exposure (AUC) (mg*h/L) · Total bevacizumab clearance · Central distribution volume
Adjustable model parameters
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More key parameters (1)
How the model represents the biology
A minimal PBPK model connecting body-weight-scaled bevacizumab clearance and compartment volumes to central and peripheral antibody exposure.
Solid arrows show modeled movement or change; two-headed arrows show reversible exchange; dashed arrows show modulation without material transfer.
Model scope: VEGF binding or pharmacodynamics, organ-resolved PBPK, FcRn trafficking, maturation or ontogeny, and explicit body-weight scaling of absolute clearance are not represented.
Modeled relationships (6)
- IV bevacizumab → Central exposure: IV input (flow)
- Central exposure ↔ Peripheral pool: distribution (reversible exchange)
- Body weight → Central exposure: scales Vc (modulation)
- Body weight → Peripheral pool: scales Vp (modulation)
- Central exposure → Total clearance: CLcat + CLadd (loss)
- Central exposure → Cumulative exposure: integrates C (production)
Modeled relationships: IV bevacizumab to Central exposure: IV input (flow); Central exposure reversibly exchanges with Peripheral pool: distribution (reversible exchange); Body weight to Central exposure: scales Vc (modulation); Body weight to Peripheral pool: scales Vp (modulation); Central exposure to Total clearance: CLcat + CLadd (loss); Central exposure to Cumulative exposure: integrates C (production).
Primary readouts: Central bevacizumab concentration; Cumulative exposure; Total clearance; Central volume.
Related models
Research use only — not for patient-specific prediction or dosing advice.