【Product for Licensing】The Phase II Small Molecule targeting IL-17 & IL-4Ra solves unmet medical needs in Psoriasis and Atopic Dermatitis

If interested, please contact DrugTimes BD Team at BD@drugtimes.cn

【Product for Licensing】The Phase II Small Molecule targeting IL-17 & IL-4Ra solves unmet medical needs in  Psoriasis and Atopic Dermatitis

Project ID:BP-20240618-OR-060

Product Brief Summary

  • Product Name: 
  • Modality: Small Molecule
  • Target: IL-17 & IL-4Ra
  • Therapeutic Area: Immunology- Psoriasis, Atopic Dermatitis
  • Current Stage: China Phase II
  • Rights Available: China/Global Right
  • Collaboration Mode: License out

Mechanism of action

  • The product decreased IL-1β、IL-6、IL-8、MCP-1、ICAM-1 in HaCaT cells stimulated by TNF-/IFN-γ
  • The product decreased the release of β-hexosaminidase and histamine in BMMCs stimulated by IgE
  • The product decreased protein levels of IL-4、TNF-α and IL-13 in BMMCs stimulated by IgE
  • The product decreased the percentage of IL-17A-producing T cells in murine spleen cells stimulated by Con A.
  • The product cream suppressed IL-17 production and proinflammatory cytokines in the psoriasis-like skin inflammation in IMQ-induced murine model.
  • The effect of blockade IL-17 both in vitro and in vivo can mainly explain why the product has potential to apply on psoriasis.
  • The product can bind to IL-4Rα, affect downstream pathways, and improve atopic dermatitis like symptoms.

Clinical needs for Psoriasis

  • Demand for fast removal of skin lesion
  • Long-term treatment and easy to relapse
  • Worry about medicine safety
  • Conventional therapies not enough

Treatment direction for Psoriasis

  • Rapid removal of lesions
  • Treatment compliance
  • Good safety
  • Control of recurrence

Clinical needs for Atopic Dermatitis

  • Long-term treatment and easy to relapse
  • Intense itch
  • A large number of adolescent patients
  • Worry about medicine safety
  • Conventional therapies not enough

Treatment direction for Atopic Dermatitis

  • Itch control
  • Treatment compliance
  • Good safety
  • Control of recurrence

The features of the candidate for psoriasis

  • Inhibition of IL-17—a pathogenic factor of psoriasis and improvement of skin lesion with the effect not weaker than glucocorticoid
  • Decrease of psoriasis-like symptoms in IMQ-induced relapse murine model
  • Good safety of topical application on skin with the PK characteristics showing high AUC in skin tissue but low in system to meet the demand of long-term treatment on psoriasis patients
  • Focusing on the First-line therapy on mild to moderate psoriasis and combination therapy or sequential therapy on moderate to severe psoriasis

The features of the candidate for Atopic Dermatitis

  • Inhibition of IL-4—a pathogenic factor of atopic dermatitis and improvement of skin lesion
  • Suppression of histamine release and intense itch
  • Good safety of topical application on skin with the PK characteristics showing high AUC in skin tissue but low in system to meet the demand of long-term treatment on Atopic Dermatitis patients
  • Focusing on mild to moderate atopic dermatitis and combination therapy or sequential therapy on moderate to severe atopic dermatitis

Pharmaceutical effects on Psoriasis

  • The product attenuated the psoriasis-like symptoms, including erythema and scaling
  • The product relieved the pathological features of psoriasis-like skin inflammation in IMQ-induced murine model.
  • The product Cream decreased psoriasis-like symptoms in IMQ-induced relapse murine model.
  • The product Cream decreased PASI score, and total pathological score in lesion skin.

Pharmaceutical effects on Atopic Dermatitis

  • The product Cream attenuated the AD-like symptoms in MC903-induced murine model, including dermatitis score, ear thickening, epidermal and dermal hyperplasia
  • The product decreased the number of mast cells in ears, and IgE protein level in serum in mice.
  • The product decreased proinflammatory cytokines, like IL-4, IL-13 and TSLP in lesion ears.

Contact

  • If interested, please contact DrugTimes BD Team at BD@drugtimes.cn. Many thanks!

发布者:qi.yang,转载请首先联系contact@drugtimes.cn获得授权

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