Drug Development Services for Erythrodermic Psoriasis
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Drug Development Services for Erythrodermic Psoriasis

Erythrodermic psoriasis (EP) is a severe and rare variant of psoriasis, characterized by extensive inflammatory erythema that can cover more than 90% of the body's surface area. Ace Therapeutics, as a leading contract service provider, is well-equipped to facilitate drug development initiatives targeting this complex dermatological disease.

Introduction to Erythrodermic Psoriasis

Erythrodermic psoriasis can be triggered by factors such as the withdrawal of systemic therapies, infections, or irritants. Clinically, EP manifests as generalized redness, scaling, and systemic symptoms like fever and fatigue. Histologically, it displays classic features of psoriasis, such as epidermal hyperplasia and a significant inflammatory infiltrate.

Current research highlights a unique immune profile associated with EP, characterized by a shift toward a T helper 2 (Th2) response. Elevated levels of cytokines like IL-4 and IL-10 have been documented, suggesting a distinct pathophysiological mechanism that may require targeted therapeutic interventions. Notable therapies in development include biologics targeting IL-17 and IL-23 pathways, which have shown promise in treating various forms of psoriasis.

Fig 1. The classic characteristics of erythrodermic psoriasisFig. 1 Classic features of psoriasis include regular epidermal hyperplasia, hypogranulosis, dilated vessels within the dermal papillae, and numerous neutrophils in the stratum corneum and epidermis. (Potter KA, et al., 2017)

Comprehensive Drug Development Services for Erythrodermic Psoriasis

At Ace Therapeutics, we specialize in providing comprehensive drug development services tailored to erythrodermic psoriasis. We employ a range of advanced methodologies to rigorously evaluate the efficacy and safety of therapeutic candidates.

Target Identification and Validation

We employ bioinformatics and molecular biology techniques to identify and validate therapeutic targets associated with the Th2-dominant immune response in erythrodermic psoriasis.

  • Genomic and Transcriptomic Analysis: Employing RNA sequencing and microarray technologies to analyze gene expression profiles in erythrodermic psoriasis models.
  • Proteomics: Using mass spectrometry to identify and quantify proteins involved in the inflammatory pathways specific to EP.

Preclinical Efficacy Evalution

Our high-throughput screening capabilities support our clients to evaluate a wide array of compounds for their efficacy against validated targets.

  • In Vitro Assays: We perform cellular assays to assess the biological activity of potential drug candidates, focusing on their ability to modulate Th2 cytokine production and other inflammatory markers.
  • Custom Model Development: Developing in vivo models tailored to client needs to better mimic the erythrodermic phenotype, thereby facilitating more relevant testing of candidate compounds.
  • Pathway Analysis: Employing techniques such as western blotting, ELISA, and flow cytometry to elucidate the signaling pathways affected by potential therapeutic agents.

Formulation Development Support

We assist clients in developing formulations that optimize drug delivery and efficacy.

  • Nanoparticle and Liposome Technologies: Developing advanced delivery systems that enhance the bioavailability of therapeutic agents, particularly for topical applications.
  • Stability Testing: Conducting studies to evaluate the long-term stability and integrity of drug formulations under various conditions, which is crucial for maintaining therapeutic efficacy.

Erythrodermic Psoriasis presents significant challenges in drug development, necessitating innovative and targeted therapeutic strategies. Ace Therapeutics is dedicated to providing the necessary preclinical research services that enable our clients to navigate these challenges effectively. Contact us today to learn more about how we can support your drug development projects.

Reference

  1. Potter KA, et al. Erythrodermic psoriasis after discontinuation of ixekizumab. JAAD Case Rep. 2017 Dec 18;4(1):22-23.
All of our services are intended for preclinical research use only and cannot be used to diagnose, treat or manage patients.