Ongoing trials with biological drugs for EGIDs
Monoclonal Antibody | Target | Clinicaltrials.gov ID | Design | Indication | Dose | Primary outcome |
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Mepolizumab | IL-5 | NCT03656380 | Placebo-controlled, phase 2 RCT | EoE | 300 mg s.c. monthly for 6 months or placebo | Mean change in dysphagia from baseline to 3 months post-treatment assessed by EEsAI |
Benralizumab | IL5Rα | NCT03473977 | Placebo-controlled, phase 2/3 RCT | EGE | 30 mg s.c. every 4 weeks or placebo | At week 12 % of patients in histological remission (< 30 eos/HPF) |
Dupilumab | IL-4Rα | NCT03678545 | Placebo-controlled, phase 2 RCT | EGE | 600 mg s.c. initial dose and 300 mg s.c. subsequent doses every two weeks for 6 injections | At week 12 relative change from baseline of the peak eosinophil counts in the 5 most eosinophil dense HPFs in the gastric antrum and/or body |
Lirentelimab (AK002) | Siglec-8 | NCT04322708 | Placebo-controlled, phase 2/3 RCT | EoE | 1 mg/kg, 3 mg/kg or placebo monthly for 6 doses | At week 24 proportion of patients achieving esophageal intraepithelial eosinophil count of ≤ 6 eos/HPF and mean absolute change DSQ score from baseline to week 23–24 |
Lirentelimab (AK002) | Siglec-8 | NCT04322604 | Placebo-controlled, phase 3 RCT | EGE | 1 mg/kg followed by 5 monthly doses of 3 mg/kg or placebo | At week 24 proportion of patients achieving eosinophil count ≤ 4 cells per HPF in 5 gastric HPF and/or eosinophil count ≤ 15 cells per HPF in 3 duodenal HPF; mean absolute change in 6 symptoms total symptom as measured by the PRO questionnaire |
Siglec-8: sialic acid-binding immunoglobulin-like lectin 8
FL: Conceptualization, Investigation, Writing—original draft, Writing—review & editing. AC: Writing—review & editing, Writing—original draft, Supervision. All authors read and approved the submitted version, and have reviewed, discussed, and agreed to their individual contributions ahead of this time.
The authors declare that they have no conflicts of interest.
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© The Author(s) 2023.