TY - JOUR
T1 - RPC4046, a Monoclonal Antibody Against IL13, Reduces Histologic and Endoscopic Activity in Patients With Eosinophilic Esophagitis
AU - HEROES Study Group
AU - Hirano, Ikuo
AU - Collins, Margaret H.
AU - Assouline-Dayan, Yehudith
AU - Evans, Larry
AU - Gupta, Sandeep
AU - Schoepfer, Alain M.
AU - Straumann, Alex
AU - Safroneeva, Ekaterina
AU - Grimm, Michael
AU - Smith, Heather
AU - Tompkins, Cindy ann
AU - Woo, Amy
AU - Peach, Robert
AU - Frohna, Paul
AU - Gujrathi, Sheila
AU - Penenberg, Darryl N.
AU - Li, Caiyan
AU - Opiteck, Gregory J.
AU - Olson, Allan
AU - Aranda, Richard
AU - Rothenberg, Marc E.
AU - Dellon, Evan S.
N1 - Publisher Copyright:
© 2019 AGA Institute
PY - 2019/2
Y1 - 2019/2
N2 - Background & aims: Eosinophilic esophagitis (EoE) is a chronic, esophageal, type 2 inflammatory response associated with increased serum levels of interleukin 13 (IL13), which might contribute to its pathogenesis. RPC4046, a recombinant humanized monoclonal antibody against IL13, prevents its binding to the receptor subunits IL13RA1 and IL13RA2. We performed a phase 2 trial to evaluate the efficacy and safety of RPC4046 in patients with EoE. Methods: We performed a multicenter, double-blind trial of 99 adults with active EoE randomly assigned (1:1:1) to groups given RPC4046 (180 or 360 mg) or placebo once weekly for 16 weeks, from September 2014 through December 2015. Patients were seen at day 1 (baseline) and weeks 2, 4, 8, 12, and 16. They underwent esophagogastroduodenoscopy and biopsies were collected at baseline and week 16. Patients completed a daily dysphagia symptom diary through week 16 and patient-reported outcome data were collected. The primary outcome was change in mean esophageal eosinophil count in the 5 high-power fields (hpfs) with the highest level of inflammation. Results: At week 16, mean changes in esophageal eosinophil count per hpf were a reduction of 94.8 ± 67.3 in patients who received 180 mg RPC4046 (P <.0001) and a reduction of 99.9 ± 79.5 in patients who received 360 mg RPC4046 (P <.0001) compared with a reduction of 4.4 ± 59.9 in patients who received placebo. The 360-mg RPC4046 group, compared with the placebo group, showed significant reductions in validated endoscopic severity score at all esophageal locations (P <.0001), validated histologic grade and stage scores (both P <.0001), and clinician's global assessment of disease severity (P =.0352); they had a numerical reduction in scores from the dysphagia symptom diary (P =.0733). Significant reductions in esophageal eosinophil counts and histologic and endoscopic features were observed in patients with steroid-refractory EoE who received RPC4046. The most common adverse events were headache and upper respiratory tract infection. Conclusions: In a phase 2 trial of patients with EoE, we found RPC4046 (a monoclonal antibody against IL13) to reduce histologic and endoscopic features compared with placebo. RPC4046 was well tolerated. ClinicalTrials.gov no: NCT02098473.
AB - Background & aims: Eosinophilic esophagitis (EoE) is a chronic, esophageal, type 2 inflammatory response associated with increased serum levels of interleukin 13 (IL13), which might contribute to its pathogenesis. RPC4046, a recombinant humanized monoclonal antibody against IL13, prevents its binding to the receptor subunits IL13RA1 and IL13RA2. We performed a phase 2 trial to evaluate the efficacy and safety of RPC4046 in patients with EoE. Methods: We performed a multicenter, double-blind trial of 99 adults with active EoE randomly assigned (1:1:1) to groups given RPC4046 (180 or 360 mg) or placebo once weekly for 16 weeks, from September 2014 through December 2015. Patients were seen at day 1 (baseline) and weeks 2, 4, 8, 12, and 16. They underwent esophagogastroduodenoscopy and biopsies were collected at baseline and week 16. Patients completed a daily dysphagia symptom diary through week 16 and patient-reported outcome data were collected. The primary outcome was change in mean esophageal eosinophil count in the 5 high-power fields (hpfs) with the highest level of inflammation. Results: At week 16, mean changes in esophageal eosinophil count per hpf were a reduction of 94.8 ± 67.3 in patients who received 180 mg RPC4046 (P <.0001) and a reduction of 99.9 ± 79.5 in patients who received 360 mg RPC4046 (P <.0001) compared with a reduction of 4.4 ± 59.9 in patients who received placebo. The 360-mg RPC4046 group, compared with the placebo group, showed significant reductions in validated endoscopic severity score at all esophageal locations (P <.0001), validated histologic grade and stage scores (both P <.0001), and clinician's global assessment of disease severity (P =.0352); they had a numerical reduction in scores from the dysphagia symptom diary (P =.0733). Significant reductions in esophageal eosinophil counts and histologic and endoscopic features were observed in patients with steroid-refractory EoE who received RPC4046. The most common adverse events were headache and upper respiratory tract infection. Conclusions: In a phase 2 trial of patients with EoE, we found RPC4046 (a monoclonal antibody against IL13) to reduce histologic and endoscopic features compared with placebo. RPC4046 was well tolerated. ClinicalTrials.gov no: NCT02098473.
KW - Esophagus
KW - Immune Response
KW - Placebo-Controlled
KW - Randomized
UR - http://www.scopus.com/inward/record.url?scp=85060994694&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85060994694&partnerID=8YFLogxK
U2 - 10.1053/j.gastro.2018.10.051
DO - 10.1053/j.gastro.2018.10.051
M3 - Article
C2 - 30395812
AN - SCOPUS:85060994694
SN - 0016-5085
VL - 156
SP - 592-603.e10
JO - Gastroenterology
JF - Gastroenterology
IS - 3
ER -