- |||||||||| cendakimab (CC-93538) / AbbVie, BMS, dectrekumab (QAX576) / Novartis, Dupixent (dupilumab) / Sanofi, Regeneron
Retrospective data, Review, Journal: Efficacy and Safety of Monoclonal Antibodies for the Treatment of Eosinophilic Esophagitis: A Systematic Review and Meta-Analysis of Randomized Controlled Trials. (Pubmed Central) - May 6, 2024 MAbs seem effective and safe in reducing esophageal eosinophil infiltrate, EoE-HSS score, EREFS score, and dysphagia symptoms in patients with EoE. However, further evidence is needed to establish its place in EoE management.
- |||||||||| Review, Journal: The New Therapeutic Frontiers in the Treatment of Eosinophilic Esophagitis: Biological Drugs. (Pubmed Central) - Feb 10, 2024
Despite the undeniable economic impact of biologic therapies, in the near future, there will be room for further reflection about the opportunity to prescribe biologic agents, not only as a last-line therapy in selected cases such as patients with comorbidities involving common pathways. Although recent findings are very encouraging, the road to permanent success in the treatment of EoE is still long, and further studies are needed to determine the long-term effects of mAbs and to discover new potential targets.
- |||||||||| budesonide / Generic mfg.
Journal: Current options and investigational drugs for the treatment of eosinophilic esophagitis. (Pubmed Central) - Feb 26, 2022 These include monoclonal antibodies (including mepolizumab, reslizumab, benralizumab, dectrekumab, cendakimab, and dupilumab), JAK-STAT blockers, and S1PR agonists, among others...Therapies under investigation potentially can target multiple Th2-associated diseases that converge in EoE patients. Therapeutic strategies require a personalized and patient-centered approach to reduce the burden of the disease, and cost-effectiveness analysis to position their use in a complex therapeutic landscape.
- |||||||||| Remicade (infliximab) / Merck (MSD), Mitsubishi Tanabe, J&J, Entyvio (vedolizumab) / Takeda, Xolair (omalizumab) / Roche, Novartis
Journal: Pharmacological treatments for eosinophilic esophagitis: current options and emerging therapies. (Pubmed Central) - Jun 30, 2021 Several additional promising therapies are also discussed.Expert opinion: Several therapeutic targets have shown efficacy and will be approved to treat EoE, especially corticosteroid-sparing options and those for patients with multiple Th2-associated diseases. Personalized therapeutic strategies for initial and maintenance treatments of EoE must be rationally designed, to reduce the burden of disease and answer meaningfully the needs of all stakeholders involved in EoE.
- |||||||||| Eosinophilic Esophagitis Drug Markets, 2028 - Budesonide Oral Suspension, Fluticasone ODT, Mepolizumab, Reslizumab, Benralizumab, Dupilunab, Omalizumab, QAX576, AKOO2, and Losartan - https://t.co/guyiBzPH8C https://t.co/S8GRJErfKm (Twitter) - Apr 19, 2021
- |||||||||| Remicade (infliximab) / Mitsubishi Tanabe, J&J, Xolair (omalizumab) / Roche, Novartis
Review, Journal: Pharmacotherapies for the Treatment of Eosinophilic Esophagitis: State of the Art Review. (Pubmed Central) - Jan 30, 2020 Additionally, anti-allergic targets, immunosuppressives, and monoclonal antibodies (such as mepolizumab, reslizumab, QAX576, RPC4046, dupilumab, omalizumab, and infliximab) that have been evaluated as treatments for EoE are summarized. Finally, several promising therapeutic agents (e.g., sialic acid-binding immunoglobulin-like lectin 8 antibodies, the transforming growth factor-β1 signal blocker losartan, CC chemokine receptor type 3 antagonists, thymic stromal lymphopoietin antibodies, antibodies targeting the α4β7 integrin, anti-interleukin-9 antibodies, and anti-interleukin-15 antibodies) that target specific molecules or cells implicated in the pathogenesis of EoE are proposed.
- |||||||||| QBX-258 / Novartis, dectrekumab (QAX576) / Novartis
Trial completion: Immunotherapy for the Treatment of Breast Cancer Related Upper Extremity Lymphedema (BCRL) (clinicaltrials.gov) - May 30, 2018 P=N/A, N=9, Completed, Finally, several promising therapeutic agents (e.g., sialic acid-binding immunoglobulin-like lectin 8 antibodies, the transforming growth factor-β1 signal blocker losartan, CC chemokine receptor type 3 antagonists, thymic stromal lymphopoietin antibodies, antibodies targeting the α4β7 integrin, anti-interleukin-9 antibodies, and anti-interleukin-15 antibodies) that target specific molecules or cells implicated in the pathogenesis of EoE are proposed. Active, not recruiting --> Completed
- |||||||||| QBX-258 / Novartis, dectrekumab (QAX576) / Novartis
Enrollment closed, Enrollment change, Trial primary completion date: Immunotherapy for the Treatment of Breast Cancer Related Upper Extremity Lymphedema (BCRL) (clinicaltrials.gov) - May 25, 2016 P=N/A, N=9, Active, not recruiting, Trial primary completion date: Jul 2017 --> Jul 2018 Recruiting --> Active, not recruiting | N=22 --> 9 | Trial primary completion date: Jul 2016 --> Jul 2017
- |||||||||| dectrekumab (QAX576) / Novartis
Enrollment change: Efficacy of QAX576 in Asthma (clinicaltrials.gov) - Aug 20, 2013 P2, N=259, Completed, N=19 --> 10 N=486 --> 259
- |||||||||| dectrekumab (QAX576) / Novartis
Enrollment change: SD, IL-13 Production Rate in IPF (clinicaltrials.gov) - Nov 26, 2012 P2, N=52, Completed, Recruiting --> Completed N=31 --> 52
- |||||||||| dectrekumab (QAX576) / Novartis
Trial completion: Efficacy of QAX576 in Asthma (clinicaltrials.gov) - May 1, 2012 P2, N=259, Completed, Active, not recruiting --> Completed Recruiting --> Completed
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