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Clinically relevant – Recapitulates human plaque psoriasis: erythema, scaling, thickening, and Th17-mediated inflammation.
Well-characterized endpoints – PASI score (erythema, scaling, thickness), skin histopathology, IL-17A and IL-36 levels, clinical photography.
Mechanism-driven – IMQ activates TLR7/8, inducing IFN-α and IL-23/IL-17 pathway, closely mimicking human disease pathogenesis.
Translational value – Ideal for testing biologics (anti-IL-17, anti-IL-23), JAK inhibitors, and topical therapies.
IND-ready data packages – Studies can be conducted in accordance with GLP principles.
Representative data from our IMQ Induced NHP Psoriasis model:
IMQ Induced Psoriasis Model in NHP

• Efficacy testing of biologics (anti-IL-17, anti-IL-23, anti-TNF), JAK inhibitors, and topical therapies
• Target validation for Th17 pathway and IL-36 signaling
• Biomarker discovery (IL-17A, IL-36, other psoriasis-related mediators)
• Mechanism of action (MOA) studies
• IND-enabling toxicology and safety pharmacology studies
Parameter | Specification |
Species | Cynomolgus macaque (Macaca fascicularis) |
Induction method | Daily topical application of 5% imiquimod (IMQ) cream for 5–14 days |
Study duration | 2–4 weeks (induction + treatment phase) |
Key endpoints | PASI score (erythema, scaling, thickness); skin histopathology (acanthosis, parakeratosis, inflammatory infiltrates); IL-17A and IL-36 levels (ELISA/qPCR); clinical photography |
Data package | Raw data, analysis reports, histology slides, clinical photographs, bioinformatics (optional) |
Q: How does IMQ induce psoriasis-like inflammation?
A: IMQ activates TLR7/8, triggering production of type I IFN-α and downstream activation of the IL-23/Th17 axis, leading to keratinocyte hyperproliferation and psoriatic inflammation.
Q: What are the key similarities with human plaque psoriasis?
A: The model exhibits erythema, scaling, thickening (PASI score), elevated IL-17A and IL-36, and histopathological features (acanthosis, parakeratosis, inflammatory infiltration) identical to human disease.
Q: Can this model be used for IND-enabling studies?
A: Yes. Studies can be conducted in accordance with GLP principles for regulatory submissions (FDA, EMA).
Q: Do you offer customized study protocols (e.g., different dosing frequencies, combination therapies)?
A: Absolutely. Our scientific team tailors IMQ application protocols, treatment schedules, and endpoint analyses to your specific drug candidate.