TY - JOUR
T1 - Intravenous anti-IL-13 mAb QAX576 for the treatment of eosinophilic esophagitis
AU - Rothenberg, Marc E.
AU - Wen, Ting
AU - Greenberg, Allison
AU - Alpan, Oral
AU - Enav, Benjamin
AU - Hirano, Ikuo
AU - Nadeau, Kari
AU - Kaiser, Sergio
AU - Peters, Thomas
AU - Perez, Antonio
AU - Jones, Ieuan
AU - Arm, Jonathan P.
AU - Strieter, Robert M.
AU - Sabo, Ronald
AU - Gunawardena, Kulasiri A.
N1 - Funding Information:
Supported by Novartis Pharma AG ( ClinicalTrials.gov Identifier: NCT01022970 ).
Publisher Copyright:
© 2014 American Academy of Allergy, Asthma & Immunology.
PY - 2015/2/1
Y1 - 2015/2/1
N2 - Background Eosinophilic esophagitis (EoE) is a chronic allergic disease with limited treatment options. Objective We evaluated QAX576, an mAb against IL-13, in the treatment of patients with EoE. Methods Patients (18-50 years) with proton pump inhibitor-resistant esophageal eosinophilia received intravenous QAX576 (6 mg/kg) or placebo (2:1) at weeks 0, 4, and 8 and were followed for 6 months. The primary end point was the responder rate for a greater than 75% decrease in peak eosinophil counts at week 12. Efficacy was to be declared if the lower 90% confidence limit for the proportion of responders on QAX576 was 35% or greater. Secondary end points included changes in esophageal eosinophil counts, symptoms assessed by questionnaire scores, and quantification of a series of biomarkers. Results Twenty-three patients completed the study up to week 12, and 18 continued to the end of the study. For the proximal and distal esophageal biopsies combined, the responder rate was 12.5% (90% confidence limit, 1% to 43%) with placebo, compared to 40.0% (90% confidence limit, 22% to 61%) with QAX576. Although the primary end point was not met, the mean esophageal eosinophil count decreased by 60% with QAX576 versus an increase of 23% with placebo (P =.004), and the decrease was sustained up to 6 months. There was a trend for improved symptoms, particularly dysphagia. QAX576 improved expression of EoE-relevant esophageal transcripts, including eotaxin-3, periostin, and markers of mast cells and barrier function, for up to 6 months after treatment. QAX576 was well tolerated. Conclusions QAX576 significantly improved intraepithelial esophageal eosinophil counts and dysregulated esophageal disease-related transcripts in adults with EoE in a sustained manner.
AB - Background Eosinophilic esophagitis (EoE) is a chronic allergic disease with limited treatment options. Objective We evaluated QAX576, an mAb against IL-13, in the treatment of patients with EoE. Methods Patients (18-50 years) with proton pump inhibitor-resistant esophageal eosinophilia received intravenous QAX576 (6 mg/kg) or placebo (2:1) at weeks 0, 4, and 8 and were followed for 6 months. The primary end point was the responder rate for a greater than 75% decrease in peak eosinophil counts at week 12. Efficacy was to be declared if the lower 90% confidence limit for the proportion of responders on QAX576 was 35% or greater. Secondary end points included changes in esophageal eosinophil counts, symptoms assessed by questionnaire scores, and quantification of a series of biomarkers. Results Twenty-three patients completed the study up to week 12, and 18 continued to the end of the study. For the proximal and distal esophageal biopsies combined, the responder rate was 12.5% (90% confidence limit, 1% to 43%) with placebo, compared to 40.0% (90% confidence limit, 22% to 61%) with QAX576. Although the primary end point was not met, the mean esophageal eosinophil count decreased by 60% with QAX576 versus an increase of 23% with placebo (P =.004), and the decrease was sustained up to 6 months. There was a trend for improved symptoms, particularly dysphagia. QAX576 improved expression of EoE-relevant esophageal transcripts, including eotaxin-3, periostin, and markers of mast cells and barrier function, for up to 6 months after treatment. QAX576 was well tolerated. Conclusions QAX576 significantly improved intraepithelial esophageal eosinophil counts and dysregulated esophageal disease-related transcripts in adults with EoE in a sustained manner.
KW - IL-13
KW - QAX576
KW - T2 cells
KW - barrier function
KW - cytokine
KW - eosinophilic esophagitis
KW - mAb
KW - mast cell
KW - randomized clinical trial
KW - targeted therapy
KW - transcriptome
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U2 - 10.1016/j.jaci.2014.07.049
DO - 10.1016/j.jaci.2014.07.049
M3 - Article
C2 - 25226850
AN - SCOPUS:84922379477
SN - 0091-6749
VL - 135
SP - 500
EP - 507
JO - Journal of Allergy and Clinical Immunology
JF - Journal of Allergy and Clinical Immunology
IS - 2
ER -