Source: ClinicalTrials.gov — U.S. National Library of Medicine — A database of privately and publicly funded clinical studies conducted around the world (U.S. National Library of Medicine, public domain).
This page lists clinical trials related to Eosinophilic Disorders from the ClinicalTrials.gov database.
Trial Summary
- Total studies: 50
- Recruiting: 21
- Active, not recruiting: 12
- Completed: 13
- Other: 4
Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.
Recruiting Trials
NCT00001406 — Activation and Function of Eosinophils in Conditions With Blood or Tissue Eosinophilia
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Allergy and Infectious Diseases (NIAID) |
| Enrollment | 800 |
| Study Type | OBSERVATIONAL |
| Conditions | Immune System Diseases; Eosinophilia; Helminthiasis; Hypersensitivity; Parasitic Disease |
This study will investigate how, why and under what conditions eosinophils (a type of white blood cell) become activated and will examine their function in immune reactions. Eosinophil counts often rise in response to allergies, asthma, and parasitic worm infections. They can also go up in uncommon autoimmune conditions and, rarely, in association with tumors. Elevated levels of these cells is …
NCT00091871 — A Longitudinal Study of Familial Hypereosinophilia (FE): Natural History and Markers of Disease Progression
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Allergy and Infectious Diseases (NIAID) |
| Enrollment | 50 |
| Study Type | OBSERVATIONAL |
| Conditions | Eosinophilia; Hypereosinophilic Syndrome |
Eosinophils are a type of white blood cell. Elevated eosinophil levels can damage the heart, nerves, and other organs, in the syndrome known as hypereosinophilic syndrome (HES). Some individuals have a hereditary form of HES known as familial eosinophilia (FE). More research on the causation and mechanisms of HES is needed in order to design more effective and less toxic therapies.
This study …
NCT01137825 — Registry of Older Patients With Cancer
| Status | Recruiting |
| Phase | N/A |
| Sponsor | UNC Lineberger Comprehensive Cancer Center |
| Enrollment | 3000 |
| Study Type | OBSERVATIONAL |
| Conditions | Chronic Myeloproliferative Disorders; Cognitive/Functional Effects; Leukemia; Lymphoma; Lymphoproliferative Disorder |
RATIONALE: Gathering information about older patients with cancer may help the study of cancer in the future.
PURPOSE: This research study is gathering information from older patients with cancer into a registry.
NCT04506593 — Indiana University Gastrointestinal Motility Diagnosis Registry
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Indiana University |
| Enrollment | 5000 |
| Study Type | OBSERVATIONAL |
| Conditions | Eosinophilic Esophagitis; Gastroesophageal Reflux Disease (GERD); Gastroparesis; Functional Vomiting; Irritable Bowel Syndrome (IBS) |
| Interventions |
Develop a registry (list of patients) with accurate clinical motility diagnosis. This registry will help the doctors to identify the patients with specific disease conditions. It will also help in promoting future research in gastroenterology motility disorders
NCT02504853 — Natural History and Genetics of Food Allergy and Related Conditions
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Allergy and Infectious Diseases (NIAID) |
| Enrollment | 1800 |
| Study Type | OBSERVATIONAL |
| Conditions | Food Allergy; Loeys-Dietz Syndrome; Atopic Dermatitis; Eosinophilic Esophagitis |
Background:
- About 15 million Americans have a food allergy. Because there are no cures or effective prevention or treatment for food allergies, researchers want to learn more about them.
Objective:
- To learn more about the causes and effects of food allergy and related conditions.
Eligibility:
- People ages 2 99 who have food allergy and/or a related genetic or other condition
- Their…
NCT03980886 — Characteristics and Inflammatory Markers in Children With Eosinophilic Esophagitis (EoE)
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of California, San Diego |
| Enrollment | 1500 |
| Study Type | OBSERVATIONAL |
| Conditions | Eosinophilic Esophagitis |
Single center observational and specimen banking study for children with eosinophilic esophagitis EoE to gauge natural history and inflammatory markers
NCT05692180 — A Multicentre, Randomised, Double-blind, Parallel Group, Placebo-controlled, Time-to-first Asthma Exacerbation Phase III Efficacy and Safety Study of Benralizumab in Paediatric Patients With Severe Eosinophilic Asthma (DOMINICA)
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | AstraZeneca |
| Enrollment | 200 |
| Study Type | INTERVENTIONAL |
| Conditions | Asthma |
| Interventions | ; |
A study to evaluate the efficacy and safety of benralizumab administered subcutaneously in patients ≥ 6 to < 18 years of age with severe eosinophilic asthma, including a well-documented history of asthma exacerbations and uncontrolled asthma receiving high-dose inhaled corticosteroid (ICS) plus at least one additional controller medication.
NCT07636252 — Ex Vivo Drug Response Profiling and Outcome Prediction in Lung Adenocarcinoma
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Sheba Medical Center |
| Enrollment | 400 |
| Study Type | OBSERVATIONAL |
| Conditions | Lung Adenocarcinoma; Malignant Pleural Effusions (Mpe) |
| Interventions |
This observational study evaluates if ex-vivo lung cancer drug sensitivity testing results correlate with the driver mutations found by genetic sequencing and if it can predict treatment response.
NCT06979323 — Depemokimab Asthma Imaging and Bronchoscopy Sub-Study
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | GlaxoSmithKline |
| Enrollment | 150 |
| Study Type | INTERVENTIONAL |
| Conditions | Asthma |
| Interventions |
Asthma is a chronic condition marked by narrowed and swollen airways due to inflammation leading to recurring symptoms that can vary and worsen unpredictably.\xa0The purpose of this study is to assess how depemokimab, a monoclonal antibody, affects the structure and function of the lungs in asthmatic participants with type 2 inflammation, characterized by an eosinophilic phenotype.
NCT06422078 — A Non-interventional, Prospective Study With Benralizumab
| Status | Recruiting |
| Phase | N/A |
| Sponsor | AstraZeneca |
| Enrollment | 300 |
| Study Type | OBSERVATIONAL |
| Conditions | Asthma, Bronchial |
This is a prospective, non-interventional, single-arm, multicenter study to investigate asthma control, and health-related quality of life (HRQL), lung function and asthma medication intake in severe eosinophilic asthma patients treated with benralizumab in a real-life setting in Germany.
NCT06693531 — A U.S. Registry of Eosinophilic Esophagitis Pediatric, Adolescent and Adult Patients Treated With DUPIXENT® As Standard of Care
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Regeneron Pharmaceuticals |
| Enrollment | 350 |
| Study Type | OBSERVATIONAL |
| Conditions | Eosinophilic Esophagitis (EoE) |
| Interventions |
This observational research study is to better understand patients with eosinophilic esophagitis (EoE) who have recently been prescribed DUPIXENT® (dupilumab).
The purpose of this research study is to look at how DUPIXENT is used in normal care of patients with EoE.
Possible benefits to others include a better understanding of EoE and helping to inform research and clinical trial design leadi…
NCT06512883 — A Trial to Investigate Benralizumab in Children With Eosinophilic Diseases
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | AstraZeneca |
| Enrollment | 14 |
| Study Type | INTERVENTIONAL |
| Conditions | Eosinophilic Granulomatosis With Polyangiitis (EGPA); Hypereosinophilia Syndrome (HES) |
| Interventions |
The main purpose of study is to assess the safety, tolerability, pharmacokinetics (PK), and efficacy of benralizumab.
NCT06972147 — Prevalence and Description of FIRE (Food Induced Immediate Response of the Esophagus) in the Pediatric Population With Eosinophilic Esophagitis
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University Hospital, Angers |
| Enrollment | 40 |
| Study Type | OBSERVATIONAL |
| Conditions | Eosinophilic Esophagitis |
A new clinical entity of eosinophilic esophagitis, Food Induced Immediate Response of the Esophagus or FIRE, has been described since 2020. Diagnostic criteria are not clearly established. Specific questioning is necessary for differential diagnosis, such as the oro-pharyngeal syndrome notably described in pollinics, or a mechanical blockage strictly speaking linked to esophagitis. The aim is t…
NCT06862206 — This is a Non-interventional, Study to Assess Demographic Characteristics and Patient Reported Outcomes in China Patients With SEA Treated With Benralizumab
| Status | Recruiting |
| Phase | N/A |
| Sponsor | AstraZeneca |
| Enrollment | 1000 |
| Study Type | OBSERVATIONAL |
| Conditions | Chronic Obstructive Pulmonary Disease |
| Interventions |
The objective of this study is to collect empirical data that elucidates the clinical profile and therapeutic efficacy of benralizumab among the patients aged 12 years and above, with severe eosinophilic asthma. The study will focus on the early treatment response, treatment outcomes and the change in asthma control of benralizumab therapy in a real-world setting in China. This study will also …
NCT07614633 — Natural History of Eosinophilic Esophagitis in Adult and Pediatric Population
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Fondazione IRCCS Policlinico San Matteo di Pavia |
| Enrollment | 200 |
| Study Type | OBSERVATIONAL |
| Conditions | Eosinophilic Esophagitis (EoE) |
Eosinophilic esophagitis (EoE) is a Th2-mediated disease induced by ingestion of ambiental and alimentary allergens. Incidence of EoE is increasing in recent years. Young male subjects are more often affected by EoE. Esophageal eosinophilic infiltrate causes different symptoms of esophageal dysfunction (i.e. dysphagia, food impaction, chest pain, heartburn). In pediatric population symptoms are…
NCT07190209 — Efficacy, Safety, and Tolerability Study of Lunsekimig Compared With Placebo in Adult Participants With Inadequately Controlled Chronic Obstructive Pulmonary Disease (COPD) Characterized by an Eosinophilic Phenotype
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Sanofi |
| Enrollment | 942 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Obstructive Pulmonary Disease |
| Interventions | ; |
This is a parallel, Phase 2b/Phase 3, 3-arm study to investigate the efficacy, safety, and tolerability of subcutaneous (SC) treatment with lunsekimig compared with placebo in adult participants (aged 40 to 80 years, inclusive) with inadequately controlled Chronic obstructive pulmonary disease (COPD) characterized by an eosinophilic phenotype.
Participation to the study consists of 3 periods: …
NCT07190222 — Efficacy, Safety, and Tolerability Study of Lunsekimig Compared With Placebo in Adult Participants With Inadequately Controlled Chronic Obstructive Pulmonary Disease (COPD), Characterized by an Eosinophilic Phenotype
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Sanofi |
| Enrollment | 942 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Obstructive Pulmonary Disease |
| Interventions | ; |
This is a parallel, Phase 2b/Phase 3, 3-arm study to investigate the efficacy, safety, and tolerability of subcutaneous (SC) treatment with lunsekimig compared with placebo in adult participants (aged 40 to 80 years, inclusive) with inadequately controlled Chronic obstructive pulmonary disease (COPD) characterized by an eosinophilic phenotype.
Participation to the study consists of 3 periods: …
NCT07112378 — A Study of Dupilumab in Small Children With an Allergic Condition of the Esophagus (Food Pipe): Eosinophilic Esophagitis
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Regeneron Pharmaceuticals |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Eosinophilic Esophagitis (EoE) |
| Interventions |
This study is researching an experimental drug called dupilumab (called “study drug”). The study is focused on children with active eosinophilic esophagitis (EoE; an inflammatory disease of the esophagus) which impacts feeding and nourishment.
The aim of the study is to see how safe, tolerable, and effective the study drug is when given for 24 weeks to children with active EoE.
The study is l…
NCT07214753 — A Real-life Observational Study in Severe Eosinophilic Asthma Adult Participant Treated With Benralizumab in Italy
| Status | Recruiting |
| Phase | N/A |
| Sponsor | AstraZeneca |
| Enrollment | 335 |
| Study Type | OBSERVATIONAL |
| Conditions | Severe Eosinophilic Asthma |
| Interventions |
This is an observational, multicenter, prospective study on patients with severe eosinophilic asthma treated with benralizumab aimed at evaluating the achievement of partial and complete clinical remission.
NCT07323654 — A Study of KT-621 Administered Orally to Adult Participants With Moderate to Severe Eosinophilic Asthma
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Kymera Therapeutics, Inc. |
| Enrollment | 264 |
| Study Type | INTERVENTIONAL |
| Conditions | Eosinophilic Asthma |
| Interventions | ; |
This Phase 2b study is designed to evaluate the safety and efficacy of KT-621 in participants with uncontrolled moderate to severe eosinophilic asthma.
The main goals of this study are to investigate how effective KT-621 is at treating uncontrolled moderate to severe eosinophilic asthma, the safety and tolerability of KT-621, and how KT-621 behaves in the body.
NCT07027826 — The Esophageal String Test as a Diagnostic Screening Tool for Eosinophilic Esophagitis Among Africans With Dysphagia in Mali and the United States
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Allergy and Infectious Diseases (NIAID) |
| Enrollment | 70 |
| Study Type | INTERVENTIONAL |
| Conditions | Dysphagia; Eosinophilic Esophagitis |
| Interventions |
Background:
Eosinophilic esophagitis (EoE) is a disease that causes inflammation in the esophagus. The esophagus is the tube that moves food from the mouth to the stomach. Diagnosing EoE currently requires a specialized tool called an endoscope. The esophageal string test (EST) is another test; the EST collects fluid from the upper digestive tract. An EST is simpler and cheaper than an endosco…
Active, Not Recruiting
NCT00544115 — Donor Peripheral Stem Cell Transplant in Treating Patients With Advanced Hematologic Cancer or Other Disorders
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | City of Hope Medical Center |
| Enrollment | 260 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Myeloproliferative Disorders; Graft Versus Host Disease; Leukemia; Lymphoma; Multiple Myeloma and Plasma Cell Neoplasm |
| Interventions | ; ; |
RATIONALE: Giving chemotherapy and total-body irradiation before a donor peripheral stem cell transplant helps stop the growth of cancer or abnormal cells. It also helps stop the patient’s immune system from rejecting the donor’s stem cells. When the healthy stem cells from a donor are infused into the patient they may help the patient’s bone marrow make stem cells, red blood cells, white blood…
NCT03822325 — Inflammatory Mediators as Potential Non-Invasive Biomarkers in Subjects With Eosinophilic Esophagitis
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Ann & Robert H Lurie Children’s Hospital of Chicago |
| Enrollment | 88 |
| Study Type | OBSERVATIONAL |
| Conditions | Eosinophilic Esophagitis |
The investigators seek to assess esophageal inflammation or lack of it in response to treatment with a novel non-invasive method that would measure eosinophil-associated inflammatory mediators in the blood and urine to determine the presence of active Eosinophilic Esophagitis. For these purposes, the investigators will correlate esophageal inflammatory mediators measured in blood and urine with…
NCT05176262 — A Prospective Study of the Four Food Elimination Diet for Treatment of Eosinophilic Esophagitis
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Ann & Robert H Lurie Children’s Hospital of Chicago |
| Enrollment | 64 |
| Study Type | OBSERVATIONAL |
| Conditions | Eosinophilic Esophagitis |
This study is to observe the efficacy of the four food elimination diet.
NCT05176249 — Prospective Database for Eosinophilic Esophagitis (EoE) of Pediatric Population
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Ann & Robert H Lurie Children’s Hospital of Chicago |
| Enrollment | 300 |
| Study Type | OBSERVATIONAL |
| Conditions | Eosinophilic Esophagitis |
Eosinophilic Esophagitis (EoE) is a chronic, immune-mediated allergic inflammatory disorder that is being diagnosed with increased frequency. Compelling evidence suggests the etiopathogenesis is allergic and the immune response is triggered by food antigens in most children afflicted with this condition. The literature characterization of EoE is descriptive and retrospective thus far. Our aim i…
NCT05083156 — Cow’s Milk Elimination for Treatment of Eosinophilic Esophagitis
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Ann & Robert H Lurie Children’s Hospital of Chicago |
| Enrollment | 54 |
| Study Type | OBSERVATIONAL |
| Conditions | Eosinophilic Esophagitis |
| Interventions |
The investigators seek to assess the efficacy of removing cow’s milk from an EoE patient’s diet. This will be determined by esophageal inflammation and clinical and histological response to the milk elimination treatment.
NCT03953300 — Benralizumab Airway Remodeling Study in Severe Eosinophilic Asthmatics
| Status | Active, not recruiting |
| Phase | Phase 4 |
| Sponsor | AstraZeneca |
| Enrollment | 75 |
| Study Type | INTERVENTIONAL |
| Conditions | Asthma |
| Interventions | ; |
The purpose of the study is to evaluate effect of benralizumab on structural and lung function changes in severe eosinophilic asthmatics.
Changes will be assessed over 48 week treatment period in patients with persistent symptoms despite standard therapy of inhaled corticosteroids (ICS) plus long acting B2-agonist (LABA) with or without additional controller medication.
Patients who complete …
NCT05263934 — Efficacy and Safety of Depemokimab Compared With Mepolizumab in Adults With Relapsing or Refractory Eosinophilic Granulomatosis With Polyangiitis (EGPA)
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | GlaxoSmithKline |
| Enrollment | 163 |
| Study Type | INTERVENTIONAL |
| Conditions | Eosinophilic Granulomatosis With Polyangiitis |
| Interventions | ; ; |
This study aims to investigate the efficacy and safety of depemokimab compared with mepolizumab in adults with relapsing or refractory EGPA receiving SoC therapy.
NCT05731128 — A Study to Investigate the Efficacy and Safety of Dupilumab Therapy Compared With Placebo in Participants Aged ≥18 Years With Moderately to Severely Active Ulcerative Colitis With an Eosinophilic Phenotype (LIBERTY-UC SUCCEED (Study in UC for Clinical Efficacy Evaluation of Dupilumab))
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | Sanofi |
| Enrollment | 68 |
| Study Type | INTERVENTIONAL |
| Conditions | Colitis Ulcerative |
| Interventions | ; |
The protocol of this Phase 2 clinical trial consists of a double-blind, placebo-controlled, parallel-group, multicenter study to evaluate the efficacy and safety of dupilumab in participants with moderately to severely active Ulcerative Colitis (UC) with an eosinophilic phenotype.
Screening period: 2 to up to 4 weeks
Treatment period:
52-week investigational medicinal product (IMP) intervent…
NCT05831176 — A Study to Learn How Well Dupilumab Works in Adult and Adolescent Participants With Eosinophilic Gastritis With or Without Eosinophilic Duodenitis and the Side Effects it May Have
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | Regeneron Pharmaceuticals |
| Enrollment | 22 |
| Study Type | INTERVENTIONAL |
| Conditions | Eosinophilic Gastritis (EoG); Eosinophilic Duodenitis (EoD); Eosinophilic Gastrointestinal Disease (EGID); Eosinophilic Gastroenteritis |
| Interventions |
This study is researching an experimental drug called dupilumab. The study is focused on participants with active eosinophilic gastritis (EoG) with or without eosinophilic duodenitis (EoD). Participants with EoD only are not eligible for enrollment. EoG and EoD are uncommon, persistent, allergic/immune diseases in which eosinophils (a type of white blood cell) gather in large numbers in the sto…
NCT06046222 — Trial of Efficacy and Safety of NS-229 Versus Placebo in Patients With Eosinophilic Granulomatosis With Polyangiitis
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | NS Pharma, Inc. |
| Enrollment | 45 |
| Study Type | INTERVENTIONAL |
| Conditions | Eosinophilic Granulomatosis With Polyangiitis; Churg-Strauss Syndrome |
| Interventions | ; |
This study will enroll male and female subjects who are 18 years of age or older with Eosinophilic Granulomatosis With Polyangiitis.
NCT06851559 — A Study in Adult Participants With EoE to Evaluate Vonoprazan 20 mg Compared to Placebo After 12 Weeks and to Evaluate Vonoprazan 20 mg Up to 24 Weeks
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | Phathom Pharmaceuticals, Inc. |
| Enrollment | 95 |
| Study Type | INTERVENTIONAL |
| Conditions | Eosinophilic Esophagitis |
| Interventions | ; |
The primary objective of this study is to assess the efficacy of vonoprazan 20 mg once daily (QD) compared to placebo QD in the number of participants with a peak eosinophilic histologic response <15 eosinophils per high-power field (eos/hpf) after 12 weeks of therapy.
NCT07649486 — Association Between Disease Severity and Clinical, Histopathological, and Eosinophilic Markers in Patients With Bullous Pemphigoid (BP-EPIC)
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Istanbul Training and Research Hospital |
| Enrollment | 50 |
| Study Type | OBSERVATIONAL |
| Conditions | Bullous Pemphigoid (BP) |
Bullous pemphigoid is an autoimmune subepidermal blistering disease characterized by eosinophilic inflammation and variable disease severity. This retrospective observational study aims to evaluate the relationship between disease severity and histopathological features, serum IgE levels, peripheral eosinophil counts, and the expression of eosinophilic cationic protein (ECP) and periostin in sk…
Not Yet Recruiting
NCT07670338 — Xuan Yin Ning Plus Bevacizumab for Malignant Pleural Effusion
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Shanghai Chest Hospital |
| Enrollment | 308 |
| Study Type | INTERVENTIONAL |
| Conditions | Malignant Pleural Effusions (Mpe) |
| Interventions | ; |
The goal of this clinical trial is to determine whether the Xuanyin Ning Formula combined with intrapleural injection of bevacizumab via chest tube drainage is effective in treating malignant pleural effusion. It will also evaluate the safety of this combination therapy. The main questions it aims to answer include:
Does the Xuanyin Ning Formula combined with intrapleural injection of bevacizu…
NCT07671001 — A Study of Depemokimab in Participants of 6 to 11 Years of Age
| Status | Not yet recruiting |
| Phase | Phase 3 |
| Sponsor | GlaxoSmithKline |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Asthma |
| Interventions |
This study is aimed at assessing depemokimab as an add-on medicine for the treatment of asthma with type-2 inflammation in participants of 6 to 11 years of age. This study will test how the body processes depemokimab, how the drug works in the body, and its safety and tolerability.
NCT07654842 — Fasenra: An Asthma Study
| Status | Not yet recruiting |
| Phase | Phase 4 |
| Sponsor | Endeavor Health |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | Eosinophilic Asthma; Severe Asthma; Severe Eosinophilic Asthma; Asthma |
| Interventions | ; |
The goal of this observational study is to learn more about the effectiveness of benralizumab (Fasenra, 30 mg every 8 weeks) in maintaining asthma control in people with severe eosinophilic asthma.
Participants will have electronic medication monitors fitted to their usual maintenance inhaler, as well as a study-provided anti-inflammatory rescue inhaler, albuterol-budesonide (AirSupra). These …
NCT07649369 — A Phase II Study to Evaluate JMKX000197 Injection Versus Cisplatin in the Treatment of Malignant Pleural Effusion
| Status | Not yet recruiting |
| Phase | Phase 2 |
| Sponsor | Shanghai Jeyou Pharmaceutical Co., Ltd. |
| Enrollment | 120 |
| Study Type | INTERVENTIONAL |
| Conditions | Malignant Pleural Effusions (Mpe) |
| Interventions | ; |
This study aims to evaluate the efficacy and safety of intrapleural JMKX000197 compared with intrapleural cisplatin in patients with malignant pleural effusion.
Completed Trials
NCT01164241 — Natural History of Severe Allergic Inflammation and Reactions
| Status | Completed |
| Phase | N/A |
| Sponsor | National Institute of Allergy and Infectious Diseases (NIAID) |
| Enrollment | 945 |
| Study Type | OBSERVATIONAL |
| Conditions | PGM3 Deficiency; Eosinophilic and/or Atopic Dermatitis; OSMR Deficiency; Primary Localized Cutaneous Amyloidosis; Hereditary Alpha-tryptasemia |
Background:
- Allergic inflammation is central to allergy-related diseases and disorders, such as asthma, food allergies, and atopic dermatitis. Atopic dermatitis, commonly called eczema is a chronic, noncontagious skin condition, usually starting in the first years of life, which causes itching and scaling of an individual s skin. Because atopic dermatitis is a common condition in children w…
NCT00852943 — Screening Protocol for Genetic Diseases of Allergic Inflammation
| Status | Completed |
| Phase | N/A |
| Sponsor | National Institute of Allergy and Infectious Diseases (NIAID) |
| Enrollment | 824 |
| Study Type | OBSERVATIONAL |
| Conditions | Eosinophilic Disease; Immune Deficiency; HaTS; Urticaria Anaphylaxis; Elevated IgE Level |
Background:
- Mast cells are responsible for most symptoms of allergic reactions. In some allergic diseases, it is unusually easy to cause mast cells to release their contents and cause allergic reactions. In other cases, mast cells grow abnormally and, in rare cases, can result in tumors. Mast cells also control other parts of the immune system.
- Understanding why mast cells behave abnormall…
NCT01988285 — Risk Factors and Biomarkers for Diagnosis and Treatment of EoE
| Status | Completed |
| Phase | N/A |
| Sponsor | University of North Carolina, Chapel Hill |
| Enrollment | 800 |
| Study Type | OBSERVATIONAL |
| Conditions | Eosinophilic Esophagitis |
| Interventions | ; |
Purpose: To validate our previously developed model of risk factors for diagnosis of eosinophilic esophagitis (EoE), and to assess the utility of serum levels of biomarkers in diagnosis and monitoring of treatment of EoE. Participants: Up to a total of 800 participants (approximately 400 with EoE and 400 without EoE) who are referred for upper endoscopy. Procedures: This is a prospective cohort…
NCT02581514 — Eosinophilia Diagnosis
| Status | Completed |
| Phase | N/A |
| Sponsor | University Hospital, Limoges |
| Enrollment | 53 |
| Study Type | INTERVENTIONAL |
| Conditions | Hypereosinophilic Syndrome |
| Interventions |
Eosinophilia, defined by a blood eosinophil granulocytes rate greater than 500 / mm3, is frequently encountered in internal medicine.
Its causes are varied: atopy, drug allergies, parasitic infections, autoimmune diseases and solid neoplasias. Over 200 etiologies have been reported, some difficult to diagnose and can be life-threatening Eosinophilia can be a diagnostic dilemma, as the etiologi…
NCT03976310 — CT Air-trapping for the Early Identification of Benralizumab Responders Among Eosinophilic Asthma Patients
| Status | Completed |
| Phase | N/A |
| Sponsor | University Hospital, Montpellier |
| Enrollment | 59 |
| Study Type | INTERVENTIONAL |
| Conditions | Asthma |
| Interventions | ; |
BenraliScan aims to obtain thoracic computed tomography imaging data to predict the future level of patient response to a monoclonal antibody. Because the clinical responses under study can take many months to manifest, early identification of patients most-likely to benefit from treatment and treatment rule-out for others will save considerable time for everybody involved.
The primary objecti…
NCT04718389 — A Study of GSK3511294 (Depemokimab) Compared With Mepolizumab or Benralizumab in Participants With Severe Asthma With an Eosinophilic Phenotype
| Status | Completed |
| Phase | Phase 3 |
| Sponsor | GlaxoSmithKline |
| Enrollment | 1717 |
| Study Type | INTERVENTIONAL |
| Conditions | Asthma |
| Interventions | ; ; |
This study will assess whether switching participants who have benefitted from mepolizumab or benralizumab to GSK3511294 (Depemokimab) is non-inferior to maintaining current treatment on the annualized rate of clinically significant exacerbations in participants with severe asthma with an eosinophilic phenotype. Throughout the study, all participants will continue their non-biologic Baseline st…
NCT04965636 — Study in Pediatrics With HypEREosinophilic Syndrome (SPHERE)
| Status | Completed |
| Phase | Phase 3 |
| Sponsor | GlaxoSmithKline |
| Enrollment | 16 |
| Study Type | INTERVENTIONAL |
| Conditions | Hypereosinophilic Syndrome |
| Interventions |
The purpose of this study is to investigate the efficacy and safety of mepolizumab in children and adolescents with hypereosinophilic syndrome (HES) who are receiving standard of care (SoC) therapy.
NCT05774184 — A Study of CDX-0159 in Patients With Eosinophilic Esophagitis
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | Celldex Therapeutics |
| Enrollment | 86 |
| Study Type | INTERVENTIONAL |
| Conditions | Eosinophilic Esophagitis |
| Interventions | ; |
The purpose of this study is to assess the efficacy and safety of barzolvolimab in adult Eosinophilic Esophagitis patients.
NCT06501274 — Capsule Sponge Study in Eosinophilic Oesophagitis
| Status | Completed |
| Phase | N/A |
| Sponsor | East and North Hertfordshire NHS Trust |
| Enrollment | 143 |
| Study Type | INTERVENTIONAL |
| Conditions | Eosinophilic Esophagitis |
| Interventions |
Open pragmatic, descriptive single site study in adult patients with non-stenotic eosinophilic oesophagitis.
To assess the clinical value of Capsule sponge in the assessment of treatment response in patients with known non-stenosing eosinophilic oesophagitis, as an alternative to gastroscopy in a real world setting.
To assess patient preference for Capsule sponge or gastroscopy. All patients …
NCT06488703 — Retrospective Analysis of Systemic Glucocorticoid Mediated Long-term Effects, Patient Pathways and Economic Burden Across Multiple Indications
| Status | Completed |
| Phase | N/A |
| Sponsor | GlaxoSmithKline |
| Enrollment | 107032 |
| Study Type | OBSERVATIONAL |
| Conditions | Asthma |
Glucocorticoids are important in the treatment of many inflammatory, allergic, immunologic, and malignant disorders. However, the adverse effects of systemic corticosteroids are one of the most common causes of iatrogenic conditions associated with chronic inflammatory diseases. Limited data are available about long-term- Systemic (cortico)steroids / systemic glucocorticoids (SCS) related side …
NCT07093008 — Comparing the Availability of AQ280 in the Body After Single Oral Doses of a Capsule Formulation Versus a Tablet for Oral Suspension Formulation
| Status | Completed |
| Phase | Phase 1 |
| Sponsor | AQILION AB |
| Enrollment | 9 |
| Study Type | INTERVENTIONAL |
| Conditions | Eosinophilic Esophagitis |
| Interventions | ; ; |
This is a Phase 1, investigator- and participant-blinded, placebo-controlled, randomized, crossover study to compare bioavailability of AQ280 following single oral doses of a capsule formulation versus a tablet for oral suspension formulation in healthy participants.
NCT07592104 — Effectiveness on Sino-Nasal Symptoms Of Mepolizumab 300
| Status | Completed |
| Phase | N/A |
| Sponsor | Fondazione Policlinico Universitario Agostino Gemelli IRCCS |
| Enrollment | 52 |
| Study Type | OBSERVATIONAL |
| Conditions | Sinus Disease; EGPA - Eosinophilic Granulomatosis With Polyangiitis; Chronic Rhinosinusitis (CRS) With and Without Nasal Polyps |
| Interventions |
OBJECTIVES The primary objective of this study is evaluating the reduction of dimension of nasal polyps measured with Nasal Polyp Endoscopic Score (NPS) The secondary objective is to evaluate the improvement in nasal symptoms and quality of life in the patient measured through symptom questionnaires, the improvements in terms of smell dysfunction and symptomatology related to eosinophilic otiti…
NCT07591753 — Long-Term Safety and Effectiveness of Mepolizumab 300 mg in Europe (Mepo LTF Study)
| Status | Completed |
| Phase | N/A |
| Sponsor | European EGPA Study Group |
| Enrollment | 591 |
| Study Type | OBSERVATIONAL |
| Conditions | Eosinophilic Granulomatosis With Polyangiitis (Churg-Strauss) (EGPA) |
| Interventions |
This observational study aims to evaluate the long-term effectiveness and safety of mepolizumab 300 mg/4 weeks in adults with eosinophilic granulomatosis with polyangiitis (EGPA) in the European real-life setting.
The main questions it aims to answer are:
- How effective is mepolizumab 300 mg/4 weeks over long-term follow-up in patients with EGPA?
- How safe is mepolizumab 300 mg/4 weeks duri…