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Bispecific exposure and ternary binding

How does absorbed bispecific exposure populate binary and ternary complexes? Explore fixed regimens and bounded dose-amplitude optimization in normalized benchmark units. No clinical dose, patient prediction, global optimum, or paper-figure agreement is claimed.

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Turnover / binding

Drug elimination rate

1/day

Suggested: 0.05–0.15. You can explore beyond this range.

0.1 → —

Absorption rate

1/day

Suggested: 0.1–0.3. You can explore beyond this range.

0.2 → —

Ternary-complex internalization rate

1/day

Suggested: 0.05–0.15. You can explore beyond this range.

0.1 → —
Simulation time
day
day
140 → 168

Time between reported samples.

day
0.25 → 1

2 changes · Variation 1

Optimize dose amplitudes

Administration times and model parameters stay fixed. Adjust starting amplitudes within the declared bounds, then compare the optimized response with the target.

Fixed-time benchmark amplitude optimization; not a clinical regimen or a paper-optimum reproduction.

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Biology

How does absorbed bispecific exposure populate binary and ternary complexes?

How does absorbed bispecific exposure populate binary and ternary complexes?

Assumptions & evidence

Assumptions & limitations

  • Explore fixed regimens and bounded dose-amplitude optimization in normalized benchmark units. No clinical dose, patient prediction, global optimum, or paper-figure agreement is claimed.

Parameter origins

  • https://github.com/Craig-Lab/DiffDose/tree/f6c39363bdd127282a555121cbe072c49dd5f276/BiTE.py (make_params, initial_state, forward RHS)

Validation & references

One or more implementation checks are available; this is not a claim of full model reproduction.

No reference paper is attached to this model.

Model details

20 parameters · 8 states · 8 equations · 5 derived outputs

Classification & API access
Therapeutic
generic bispecific ligand
Modality
Bispecific antibody / T-cell engager
Target
generic binding partner A, generic binding partner B
Disease / scope
Mechanism-agnostic bispecific binding research
ParameterDefaultUnitDescription
Apparent distribution volumeV3dimensionlessBenchmark volume ratio
K12k1201/dayk12
K21k210.031/dayk21
Absorption rate constantka0.21/dayAbsorption rate
Degradation rate akdegA0.11/daykdegA
Degradation rate bkdegB0.11/daykdegB
Elimination rate constantkel0.11/dayDrug elimination rate
Kint akintA0.051/daykintA
Ternary complex internalization ratekintAB0.11/dayTernary-complex internalization rate
Kint bkintB0.051/daykintB
KOFF1koff10.011/daykoff1
KOFF2koff20.011/daykoff2
KOFF3koff30.011/daykoff3
KOFF4koff40.011/daykoff4
KON1kon1101/daykon1
KON2kon211/daykon2
KON3kon311/daykon3
KON4kon4101/daykon4
Ksyn aksynA11/dayksynA
Ksyn bksynB101/dayksynB

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