IMMUNOLOGY & INFLAMMATION MODEL

Atopic Dermatitis Mouse Models

Documented atopic-dermatitis platforms include OXA-, DNCB-, FITC-, and MC903-induced mouse models for inflammatory skin-disease pharmacology.

Induction format, treatment route, study window, skin assessment, tissue collection, and biomarker package are selected around the program objective.

MODEL OVERVIEW

Multiple induced mouse formats for atopic dermatitis pharmacology.

The reviewed partner portfolios include several induced atopic-dermatitis models, enabling study design to be matched to candidate mechanism, route of administration, treatment duration, and required skin or biomarker outputs.

Therapeutic areaAtopic dermatitis
SpeciesMouse
Model formatOXA, DNCB, FITC, MC903
Typical useEfficacy, Skin pathology, Biomarkers
TYPICAL APPLICATIONS

What this model can support.

01

Anti-inflammatory efficacy

Evaluate candidate activity in a selected induced atopic-dermatitis mouse model.

02

Topical or systemic dosing

Align route and formulation with the intended product profile when technically appropriate.

03

Skin tissue analysis

Collect protocol-defined skin samples for histology, molecular analysis, or other downstream work.

04

PK/PD & biomarkers

Integrate exposure, pharmacodynamic, and inflammatory biomarker measurements when required.

COMMON READOUTS

Readouts selected around the study question.

Endpoints are finalized with the selected model, species or strain, treatment design, and partner laboratory before study placement.

Skin phenotype

Protocol-defined skin-disease and treatment-response assessments.

Histopathology

Skin tissue collection and histology according to the selected protocol.

Biomarkers

Inflammatory or mechanism-linked biomarker measurements selected for the program.

Exposure

Systemic or selected tissue exposure when PK/PD work is incorporated.

Exact induction regimen, mouse strain, treatment window, skin assessment, pathology, and biomarker package are confirmed during technical review.

STUDY DESIGN

Key factors aligned before execution.

  • OXA, DNCB, FITC, or MC903 model format
  • Candidate mechanism
  • Topical or systemic dosing strategy
  • Treatment timing and duration
  • Skin assessment and histology plan
  • PK/PD and biomarker requirements

Discuss Your Program

Share the compound, mechanism, development question, preferred model, and intended endpoints. We can review fit, feasibility, and the appropriate partner-laboratory route for a Atopic Dermatitis study.Required fields are marked with an asterisk(*).

What are you developing?
What should the study help evaluate?

Briefly describe what you are developing, what you want to evaluate, what material you have available, and any timeline or study requirements.

Your contact