Aquinox Pharmaceuticals has opened Phase 2 KINSHIP study of AQX-1125 in atopic dermatitis
The following alert is from our UpdatesPlus service. This service monitors and analyzes breaking journal articles, clinical trials and R&D news across the inflammatory disease spectrum - to access our most recent issue of UpdatesPlus-Atopic Dermatitis including a full development landscape and clinical  timeline please contact fiona.watts@leaddiscovery.co.uk 
Comments: AQX-1225 has already demonstrated anti-inflammatory activity in preclinical studies, reducing release of various cytokines including GM-CSF, IL-6, TNF alpha, IL-2 and IL-4 from splenocytes. Chemotaxic was also reduced when a range of inflammatory cells and chemotactic agents were probed. In vivo, AQX-1225 has demonstrated efficacy in experimental models of atopic inflammation (passive cutaneous anaphylaxis and OVA-induced asthma models) and neutrophilic inflammation (cigarette smoke-induced pulmonary inflammation). In the clinic, oral AQX-1225 demonstrated a linear PK profile and good safety. In addition, efficacy has been demonstrated in a clinical model of COPD. This model involves administration of LPS to volunteers, which results in neutrophil elevation in the sputum. AQX-1225 reduced neutrophil counts by 62% [company data]. Since this study, Phase 2 studies have opened for interstitial cystitis/bladder pain syndrome and COPD. COPD is the lead indication with this study enrolling 400 patients
    - AQX-1125 is an oral SHIP1 activator that has been shown to reduce immune cell activation and migration
 - SHIP1 is a protein preferentially
          expressed in haematopoietic cells and which inhibits the PI3K
          pathway 
 - The atopic dermatitis study is enrolling 50 adult patients with mild-moderate disease
 - The primary endpoint is change in Total
          Lesion Symptom Score (TLSS) after 12wks.  Data are expected by
          the end of 2015
 
Comments: AQX-1225 has already demonstrated anti-inflammatory activity in preclinical studies, reducing release of various cytokines including GM-CSF, IL-6, TNF alpha, IL-2 and IL-4 from splenocytes. Chemotaxic was also reduced when a range of inflammatory cells and chemotactic agents were probed. In vivo, AQX-1225 has demonstrated efficacy in experimental models of atopic inflammation (passive cutaneous anaphylaxis and OVA-induced asthma models) and neutrophilic inflammation (cigarette smoke-induced pulmonary inflammation). In the clinic, oral AQX-1225 demonstrated a linear PK profile and good safety. In addition, efficacy has been demonstrated in a clinical model of COPD. This model involves administration of LPS to volunteers, which results in neutrophil elevation in the sputum. AQX-1225 reduced neutrophil counts by 62% [company data]. Since this study, Phase 2 studies have opened for interstitial cystitis/bladder pain syndrome and COPD. COPD is the lead indication with this study enrolling 400 patients
![]()  | 
| AQX-1225 has previously demonstrated
        efficacy in the  PCA model, a simple assay of dermal inflammation  | 


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