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 Allergy from the ClinicalTrials.gov database.
Trial Summary
- Total studies: 50
- Recruiting: 25
- Active, not recruiting: 7
- Completed: 10
- Other: 8
Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.
Recruiting Trials
NCT00001532 — Role of Genetic Factors in the Development of Lung Disease
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Heart, Lung, and Blood Institute (NHLBI) |
| Enrollment | 3500 |
| Study Type | OBSERVATIONAL |
| Conditions | Cystic Fibrosis; Pulmonary Fibrosis; Tuberous Sclerosis; Asthma; Pulmonary Sarcoidosis |
This study is designed to evaluate the genetics involved in the development of lung disease by surveying genes involved in the process of breathing and examining the genes in lung cells of patients with lung disease.
The study will focus on defining the distribution of abnormal genes responsible for processes directly involved in different diseases affecting the lungs of patients and healthy v…
NCT00605878 — Studies of Skin Microbes in Healthy People and in People With Skin Conditions
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Human Genome Research Institute (NHGRI) |
| Enrollment | 530 |
| Study Type | OBSERVATIONAL |
| Conditions | Eczema; Atopic Dermatitis |
This study will examine microbes (e.g., bacteria, fungi, viruses) that live on human skin and how microbes contribute to health and disease. It will analyze healthy human skin and how the these microorganisms might change in patients with atopic dermatitis (AD), a skin condition also known as eczema.
Healthy volunteers, as well as patients with moderate to severe eczema (AD), between 2 and 40 …
NCT00341237 — Personalized Environment and Genes Study
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Environmental Health Sciences (NIEHS) |
| Enrollment | 25000 |
| Study Type | OBSERVATIONAL |
| Conditions | Diabetes; Heart Disease; Asthma |
Despite the overwhelming focus on genetic and genomic causes of human disease over the past two decades, it has been estimated that genetics is currently known to explain only 20% and 40% of the etiology of common disease. Thus, it is becoming increasingly apparent that human disease is a consequence of both genetic susceptibility and environmental exposures. Importantly, while individuals cann…
NCT01631617 — Effects of Treatments on Atopic Dermatitis
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) |
| Enrollment | 130 |
| Study Type | INTERVENTIONAL |
| Conditions | Eczema; Dermatitis; Skin Diseases, Genetic; Dermatitis, Atopic; Skin Diseases |
| Interventions | ; ; |
Background:
- Atopic dermatitis, or eczema, is a chronic skin disorder. Patients sometimes have infections with S. aureus bacteria. Researchers want to study how eczema treatments affect the number and the type of bacteria on the skin.
Objectives:
- To study the effect of eczema treatments on skin bacteria.
Eligibility:
- Individuals between 2 and 25 years of age who have moderate to sev…
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
NCT05579366 — Rinatabart Sesutecan (Rina-S, PRO1184, GEN1184) for Advanced Solid Tumors (GCT1184-01/ PRO1184-001)
| Status | Recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Genmab |
| Enrollment | 884 |
| Study Type | INTERVENTIONAL |
| Conditions | High Grade Epithelial Ovarian Cancer; High Grade Serous Ovarian Cancer; Primary Peritoneal Carcinoma; Fallopian Tube Cancer; Endometrial Cancer |
| Interventions | ; ; |
This study will test the safety, including side effects, and determine the characteristics of a drug called Rina-S in participants with solid tumors.
Participants will have solid tumor cancer that has spread through the body (metastatic) or cannot be removed with surgery (unresectable).
NCT05689151 — A Study to Learn About Abrocitinib in Adult Patients With Moderate to Severe Atopic Dermatitis.
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Pfizer |
| Enrollment | 183 |
| Study Type | OBSERVATIONAL |
| Conditions | Atopic Dermatitis; Eczema |
| Interventions |
The purpose of this study is to learn about the safety and effects of Abrocitinib in the real-life clinical setting given for the treatment of moderate to severe atopic dermatitis. Atopic dermatitis, or AD, is a long-lasting disease that causes inflammation, redness, and irritation of the skin.
This study is seeking participant who are older than 18 years with moderate-to-severe chronic AD. Pa…
NCT05942300 — CPI-0209 Plus Carboplatin in Patients With Platinum Sensitive Recurrent Ovarian Cancer
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Lan Coffman |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Recurrent Ovarian Cancer |
| Interventions | ; |
This is a clinical trial using CPI-0209 in combination with Carboplatin chemotherapy followed by CPI-0209 maintenance in patients with platinum sensitive, recurrent ovarian cancer.
NCT06311682 — A Trial to Evaluate the Efficacy and Safety of Tralokinumab in Combination With Topical Corticosteroids in Children and Infants With Moderate-to-severe Atopic Dermatitis
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | LEO Pharma |
| Enrollment | 195 |
| Study Type | INTERVENTIONAL |
| Conditions | Atopic Dermatitis |
| Interventions | ; |
The purpose of this trial is to test whether treatment with tralokinumab (administered subcutaneous injections [SC]) in combination with topical corticosteroids (TCS) is safe and effective to treat moderate-to-severe atopic dermatitis (AD) in children and infants. This will be judged by a range of assessments that rate the severity and extent of atopic dermatitis and its symptoms, as well as …
NCT07005154 — A Phase 2 Study to Evaluate the Effects of ASP5541 in Participants With Prostate Cancer
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Astellas Pharma Global Development, Inc. |
| Enrollment | 218 |
| Study Type | INTERVENTIONAL |
| Conditions | Prostate Cancer; Metastatic Castration-Resistant Prostate Cancer; Metastatic Hormone Sensitive Prostate Cancer |
| Interventions | ; ; |
Hormone therapy, or androgen deprivation therapy (ADT) is a standard way to treat prostate cancer. It works by reducing the amount of the main male sex hormone, testosterone in the body. Androgen receptor pathway inhibitors (ARPIs) are another type of hormone therapy. They either slow down how much testosterone is made or block testosterone from reaching the prostate cancer cells. Abiraterone a…
NCT07690345 — Fungal Status and Prognosis in ABPA
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Qianfoshan Hospital |
| Enrollment | 114 |
| Study Type | OBSERVATIONAL |
| Conditions | ABPA; Allergic Bronchopulmonary Aspergillosis; Allergic Bronchopulmonary Aspergillosis (ABPA); Colonization |
This multicenter bidirectional cohort study aims to investigate the clinical characteristics and prognostic outcomes of patients with allergic bronchopulmonary aspergillosis (ABPA) stratified by fungal microbiological status in sputum or bronchoalveolar lavage fluid (BALF).
Patients diagnosed with ABPA according to the ISHAM 2024 criteria will be classified into fungal-positive and fungal-nega…
NCT07406282 — A Study to Learn About Real-world Utilization and Outcomes of Darolutamide and Other Androgen Receptor Pathway Inhibitors (ARPIs) for Newly Diagnosed Metastatic Hormone-sensitive Prostate Cancer (de Novo mHSPC) in US Urology Clinics
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Bayer |
| Enrollment | 1400 |
| Study Type | OBSERVATIONAL |
| Conditions | Prostatic Neoplasms; Metastatic Hormone-Sensitive Prostate Cancer |
| Interventions | ; ; |
Prostate cancer is the most common non-skin cancer among men in the United States. For some men, the cancer has already spread to other parts of the body at the time of diagnosis; this is called metastatic hormone-sensitive prostate cancer (mHSPC). Treatment for mHSPC has advanced significantly, with new standards of care involving androgen deprivation therapy (ADT) combined with drugs known as…
NCT07219173 — A Study to Evaluate Brenipatide Compared With Placebo in Adult Participants With Uncontrolled Moderate to Severe Asthma
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Eli Lilly and Company |
| Enrollment | 531 |
| Study Type | INTERVENTIONAL |
| Conditions | Asthma |
| Interventions | ; ; |
The purpose of this study is to assess the safety and efficacy of brenipatide at different dose levels compared with placebo in participants with moderate-to-severe asthma.
Study participation will last approximately 65 weeks, including screening, treatment, and follow-up periods.
NCT07213804 — A Three-Part Phase 3 Study of Sofetabart Mipitecan in Participants With Platinum-Resistant (Part A) and Platinum-Sensitive (Parts B and C) Ovarian Cancer
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Eli Lilly and Company |
| Enrollment | 1630 |
| Study Type | INTERVENTIONAL |
| Conditions | Ovarian Neoplasms; Fallopian Tube Neoplasms; Peritoneal Neoplasms; Neoplasm Metastasis |
| Interventions | ; ; |
This is a clinical study that has three parts. It is testing a potential new medicine called Sofetabart Mipitecan (Sofe-M) for people with certain types of ovarian, peritoneal, and fallopian tube cancers. Part A enrolls participants with platinum-resistant cancer, meaning their disease progressed during or within six months of platinum-based chemotherapy. Parts B and C enroll participants with …
NCT07288138 — A Study of a Thyroid Hormone Receptor Beta Isoform (THRβ) Agonist and an Semicarbazide Sensitive Amine Oxidase (SSAO) Inhibitor, Alone and in Combination, in Adults With Presumed Metabolic Dysfunction-associated Steatohepatitis (MASH)
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Eccogene |
| Enrollment | 160 |
| Study Type | INTERVENTIONAL |
| Conditions | Metabolic Dysfunction-associated Steatohepatitis |
| Interventions | ; ; |
The primary objective of this trial is to evaluate the dose-dependent and comparative effects of ECC4703 (low and high dose), ECC0509 (low and high dose), and their combination on hepatic fat reduction as assessed by change in magnetic resonance imaging proton density fat fraction (MRI-PDFF) at Week 12.
NCT07602192 — Quantitative Chest CT and Multi-Omics to Distinguish Asthma From COPD and Predict Treatment Response
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Korea University Guro Hospital |
| Enrollment | 200 |
| Study Type | OBSERVATIONAL |
| Conditions | Asthma (Diagnosis); COPD (Chronic Obstructive Pulmonary Disease) |
This study aims to improve the diagnosis and treatment prediction of asthma and chronic obstructive pulmonary disease (COPD) by combining quantitative chest computed tomography (CT) imaging with multi-omics data.
Adults with asthma or COPD will be enrolled and undergo routine clinical evaluations, pulmonary function tests, blood tests, and chest CT scans. Additional samples, such as sputum and…
NCT07223697 — A Long Term Extension Study to Evaluate the Safety and Efficacy of Afimkibart (RO7790121) in Participants With Atopic Dermatitis
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Hoffmann-La Roche |
| Enrollment | 120 |
| Study Type | INTERVENTIONAL |
| Conditions | Atopic Dermatitis |
| Interventions |
This study will assess long-term safety and efficacy of Afimkibart (also known as RO7790121) in participants with Atopic Dermatitis (AD) who participated in previous afimkibart clinical trials.
NCT07605078 — Associations Between Household Mold Levels and Physical and Mental Health: A Mold and Mycotoxin Testing Research Registry
| Status | Recruiting |
| Phase | N/A |
| Sponsor | OvationLab |
| Enrollment | 2500 |
| Study Type | OBSERVATIONAL |
| Conditions | Mold Illness; Mold or Dust Allergy |
| Interventions |
The primary purpose of this study is to evaluate cross-sectional associations between mold exposures identified with The Dust Test and self-reported physical health, emotional health, and medical diagnoses. In addition, associations between mold exposures and mycotoxin levels among users who have done mycotoxin lab testing will also be evaluated.
NCT07592585 — Phase III Clinical Study of VC005 in Adult and Adolescents With Mild to Moderate Atopic Dermatitis
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Jiangsu vcare pharmaceutical technology co., LTD |
| Enrollment | 360 |
| Study Type | INTERVENTIONAL |
| Conditions | Atopic Dermatitis |
| Interventions | ; |
A multicenter, randomized, double-blind, vehicle controlled phase III clinical study to evaluate the efficacy and safety of VC005 in adults and adolescents with mild to moderate atopic dermatitis
NCT07687524 — LOVING (Learning About Our Behavior is Valuable for Increasing Nurturing Relationships and Healthy Growth) RCT
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National University of Singapore |
| Enrollment | 624 |
| Study Type | INTERVENTIONAL |
| Conditions | Child Development; Child Behavioral Problems; Parent Child Relationship |
| Interventions | ; ; |
The LOVING study is a randomized controlled trial designed to determine whether adaptations to an internationally recognized parenting program that enhances sensitive caregiving likewise improves sensitive caregiving in Singapore and, in turn, downstream child outcomes in emotional, behavioral, and cognitive development during the early childhood years.
Research shows that sensitive caregiving…
NCT07598383 — A Multicenter, Randomized, Double-blind, Vehicle Controlled Phase II Clinical Study to Evaluate the Efficacy and Safety of VC005 Gel in Adult Subjects With Mild to Moderate Atopic Dermatitis
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Jiangsu vcare pharmaceutical technology co., LTD |
| Enrollment | 120 |
| Study Type | INTERVENTIONAL |
| Conditions | Atopic Dermatitis |
| Interventions | ; |
This is a multicenter, randomized, double-blind, vehicle controlled phase II clinical study to evaluate the efficacy and safety of VC005 gel in adult subjects with mild to moderate atopic dermatitis
NCT07619820 — A Phase 1b Study to Evaluate the PK of CSL300 (Clazakizumab) in Chinese Subjects With End Stage Kidney Disease (ESKD)
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | CSL Behring |
| Enrollment | 24 |
| Study Type | INTERVENTIONAL |
| Conditions | End Stage Kidney Disease (ESKD) |
| Interventions | ; |
This is a phase 1b, partial-blind (Sponsor unblinded), randomized, multicenter, placebo-controlled study. The primary objective of this study is to evaluate the pharmacokinetics (PK) of CSL300 after single and multiple doses in Chinese participants with end stage kidney disease (ESKD) undergoing dialysis.
NCT07546981 — Efficacy and Safety of CHF 5993 100/6/12.5 μg HFA-152a pMDI in Patients With Asthma Uncontrolled on Medium Doses of Inhaled Corticosteroids in Combination With Long-acting ß2-agonists
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Chiesi Farmaceutici S.p.A. |
| Enrollment | 554 |
| Study Type | INTERVENTIONAL |
| Conditions | Asthma |
| Interventions | ; |
This is a study comparing CHF 5993 pMDI HFA-152a with CHF 1535 pMDI HFA-134a in Chinese patients with asthma uncontrolled on medium doses of ICS+LABA.
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…
NCT07262983 — Evaluating the Safety and Tolerability of Baricitinib in Patients With Job Syndrome With Lupus-Like Disease and/or Atopic Dermatitis
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | National Institute of Allergy and Infectious Diseases (NIAID) |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Hyper IgE Syndrome From STAT3 Mutation; Job s Syndrome; HIES; Lupus; Atopic Dermatitis |
| Interventions |
Background:
Autosomal dominant hyper-IgE syndrome (HIES), also called Job syndrome, is a genetic disorder that affects the immune system. It can cause skin and lung infections and problems with blood vessels, connective tissues, and bones. People with HIES often have lupus-like disease or atopic dermatitis (skin rash). Researchers want to know if a drug approved to treat other immune system di…
Active, Not Recruiting
NCT00719719 — Cause of Unexplained Anaphylaxis
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | National Institute of Allergy and Infectious Diseases (NIAID) |
| Enrollment | 115 |
| Study Type | OBSERVATIONAL |
| Conditions | Idiopathic Anaphylaxis; Drug Anaphylaxis; Venom Anaphylaxis; Food Anaphylaxis |
This study will explore the possible cause of unexplained, or idiopathic, anaphylaxis. Anaphylaxis is a rapid, life-threatening, severe reaction that occurs suddenly after contact with an allergy-causing substance, usually a particular food, drug or stinging insect. The allergen triggers mast cells to release several substances, including histamine. Histamine is responsible for many of the symp…
NCT01759186 — Airway Redox and Gender Determinants in Severe Asthma
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | The Cleveland Clinic |
| Enrollment | 300 |
| Study Type | OBSERVATIONAL |
| Conditions | Asthma |
The investigators will study the biologic and chemical differences that cause the greater incidence, and severity of asthma in women as compared to men. Severe asthma affects boys more than girls, while severe asthma in adults is predominantly a disease of women. The investigators aim to identify the processes that occur in the body that are behind the onset of severe asthma in young women duri…
NCT05794906 — A Study to Compare Darolutamide Given With Androgen Deprivation Therapy (ADT) and Placebo Given With ADT in Men With Hormone Sensitive Prostate Cancer and Raise of Prostate Specific Antigen (PSA) Levels After Local Therapies
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | Bayer |
| Enrollment | 985 |
| Study Type | INTERVENTIONAL |
| Conditions | Biochemically Recurrent Prostate Cancer |
| Interventions | ; ; |
Researchers are looking for a better way to treat men at high-risk of biochemical recurrence (BCR) of prostate cancer.
BCR means that in men who had prostate cancer and were treated by either surgery and/ or radiation therapy, the blood level of a specific protein called PSA rises. PSA is a marker of prostate cancer cells activity. The PSA increase means that the cancer has come back even thou…
NCT05851443 — A Study to Evaluate the Efficacy and Safety Study of Povorcitinib in Participants With Inadequately Controlled Moderate to Severe Asthma
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | Incyte Corporation |
| Enrollment | 247 |
| Study Type | INTERVENTIONAL |
| Conditions | Moderate to Severe Asthma |
| Interventions | ; ; |
The study is being conducted to evaluate the effect of 3 dosing regimens of povorcitinib on pulmonary function
NCT06874114 — An Observational Study to Learn More About Treatment Patterns and Factors Determining the Choice of Treatment in Canadian Men With Metastatic Hormone Sensitive Prostate Cancer in Routine Medical Care
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Bayer |
| Enrollment | 700 |
| Study Type | OBSERVATIONAL |
| Conditions | Metastatic Hormone-sensitive Prostate Cancer |
This is an observational study in which only data are collected from adult Canadian men with metastatic hormone sensitive prostate cancer (mHSPC) are studied. Participants will not receive any advice on treatment or any changes to the healthcare.
Metastatic hormone sensitive prostate cancer is a cancer of the prostate gland, a male reproductive gland found below the bladder. Metastatic means t…
NCT06853626 — One-hoUr Troponin Using a High-sensitivity Point-Of-Care Assay in Emergency Primary Care
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | University of Oslo |
| Enrollment | 2500 |
| Study Type | INTERVENTIONAL |
| Conditions | Acute Myocardial Infarction (AMI); Chest Pain; Acute Coronary Syndromes (ACS); Non-cardiac Chest Pain; Troponin |
| Interventions |
Acute chest pain is a prevalent medical emergency in primary emergency care settings. Triage of chest pain prior to hospital admission presents significant challenges due to the absence of sufficiently sensitive diagnostic tools. Clinical signs, symptoms, risk assessment scores, or a normal electrocardiogram (ECG) can reliably exclude acute myocardial infarction (MI). This diagnostic uncertaint…
NCT07344779 — A Study to Learn How Men With Advanced Prostate Cancer Respond to Treatment With Darolutamide and Hormone Therapy, With or Without Chemotherapy, in Real-world Medical Practice
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Bayer |
| Enrollment | 1600 |
| Study Type | OBSERVATIONAL |
| Conditions | Metastatic Hormone-Sensitive Prostate Cancer |
| Interventions | ; ; |
This is an international, prospective, open-label, multicenter, multi-cohort, non-interventional observational study designed to describe the real-world effectiveness and safety of darolutamide in combination with androgen deprivation therapy (ADT), with or without docetaxel, in patients with metastatic hormone-sensitive prostate cancer (mHSPC). The study aims to enroll approximately 1,600 male…
Not Yet Recruiting
NCT07688772 — A Clinical Study Evaluating the Efficacy and Safety of SHR-1819 Injection in Patients With Seasonal Allergic Rhinitis
| Status | Not yet recruiting |
| Phase | Phase 3 |
| Sponsor | Guangdong Hengrui Pharmaceutical Co., Ltd |
| Enrollment | 196 |
| Study Type | INTERVENTIONAL |
| Conditions | Seasonal Allergic Rhinitis |
| Interventions | ; |
This study is a multicenter, randomized, double-blind, placebo-controlled Phase III clinical trial aimed at evaluating the efficacy, safety, pharmacokinetics (PK), pharmacodynamics (PD), and immunogenicity of SHR-1819 injection in patients with Seasonal Allergic Rhinitis (SAR).
NCT07564141 — Study to Assess the Efficacy and Safety of Rina-S With or Without Bevacizumab Compared to Investigator’s Choice of Platinum-based Chemotherapy With or Without Bevacizumab as Second-line Treatment in Participants With Recurrent Platinum-sensitive Ovarian Cancer
| Status | Not yet recruiting |
| Phase | Phase 3 |
| Sponsor | Genmab |
| Enrollment | 688 |
| Study Type | INTERVENTIONAL |
| Conditions | Platinum-Sensitive Ovarian Cancer; Ovarian Cancer |
| Interventions | ; ; |
This Phase 3 study will be conducted in different countries around the world with up to about 688 participants.
The purpose of this study is to evaluate how well Rina-S works against ovarian cancer in combination with or without bevacizumab and how it compares to an investigator’s choice of platinum-based chemotherapy with or without bevacizumab.
Participants will receive either:
- Rina-S mo…
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 …
NCT05713799 — Trial of the Combination of Alpha-Lipoic Acid and Mirabegron in Women and in Men With Obesity
| Status | Not yet recruiting |
| Phase | Phase 2 |
| Sponsor | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Insulin Resistance; Obesity |
| Interventions | ; ; |
Background:
Obesity and related illnesses cause at least 2.8 million deaths each year worldwide. Few treatments exist for obesity that are safe and widely available. A study drug (mirabegron [MG]) combined with a supplement (alpha-lipoic acid [ALA]) may help.
Objective:
To learn how MG and ALA can help the body process food.
Eligibility:
People aged 18 to 65 years with a body mass inde…
NCT06960759 — Mechanisms of Change in Behavioral Cough Suppression Therapy for Refractory Chronic Cough
| Status | Not yet recruiting |
| Phase | Phase 2 |
| Sponsor | University of Montana |
| Enrollment | 135 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Cough (CC); Refractory Chronic Cough; Unexplained Chronic Cough |
| Interventions | ; |
This study is testing new ways to help people who have chronic cough that has not improved with typical treatments. One approach is called behavioral cough suppression (BCS) therapy, which teaches people techniques to stop themselves from coughing. Another approach uses a natural substance thought to help reduce the body’s sensitivity to cough triggers.
In this study, we will test two treatmen…
NCT07686484 — A Trial of HRS-3095 in Healthy Volunteers
| Status | Not yet recruiting |
| Phase | Early Phase 1 |
| Sponsor | Atridia Pty Ltd. |
| Enrollment | 36 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Spontaneous Urticaria |
| Interventions | ; ; |
The purpose of this study is to assess safety, PK, Pharmacodynamic profile of a single dose of HRS-3095 in healthy participants
NCT07687797 — Partially Hydrolysed Whey Based Formula in Differentiation Between Non IgE Gastrointestinal Cow’s Milk Protein Allergy and Milk Intolerance
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Ain Shams University |
| Enrollment | 100 |
| Study Type | INTERVENTIONAL |
| Conditions | Cow Milk Protein Allergy; Cow Milk Intolerance |
| Interventions | ; |
Partially hydrolysed whey based formula in differentiation between non IgE gastrointestinal cow’s milk protein allergy and milk intolerance
NCT07504588 — Sacituzumab Govitecan With Bevacizumab Compared to Usual Chemotherapy (Carboplatin, Pegylated Liposomal Doxorubicin and Bevacizumab) for Treating Recurrent Platinum-Sensitive Ovarian Cancer After PARP Inhibitor Maintenance Therapy
| Status | Not yet recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 87 |
| Study Type | INTERVENTIONAL |
| Conditions | Recurrent Platinum-Sensitive Fallopian Tube Endometrioid Adenocarcinoma; Recurrent Platinum-Sensitive Fallopian Tube High Grade Serous Adenocarcinoma; Recurrent Platinum-Sensitive Ovarian High Grade Endometrioid Adenocarcinoma; Recurrent Platinum-Sensitive Ovarian High Grade Serous Adenocarcinoma; Recurrent Platinum-Sensitive Primary Peritoneal Endometrioid Adenocarcinoma |
| Interventions | ; ; |
This phase II trial compares the effect of sacituzumab govitecan and bevacizumab to standard care (carboplatin, pegylated liposomal doxorubicin, and bevacizumab) in patients with ovarian cancer that has come back after an initial response to platinum therapy (platinum-sensitive), that has progressed after poly (adenosine diphosphate-ribose) polymerase (PARP) inhibitor maintenance therapy (recur…
Completed Trials
NCT00001888 — Sample Collections From the Airways of Asthmatic Patients
| Status | Completed |
| Phase | N/A |
| Sponsor | National Heart, Lung, and Blood Institute (NHLBI) |
| Enrollment | 574 |
| Study Type | OBSERVATIONAL |
| Conditions | Asthma |
Fiberoptic bronchoscopy is a procedure which involves passing a pencil-thin tube into the lung in order to collect fluid and cells from the airways. Fiberoptic bronchoscopy can collect cells from the walls of airways by gently brushing them (bronchial brushing). In addition, squirting small amounts of sterile water in to the airway and gently suctioning it back into the bronchoscope (bronchoalv…
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…
NCT02745613 — Type 2 Diabetes Affect Exercise Induced Improvement in Insulin Sensitivity
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Texas, El Paso |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Insulin Sensitivity/Resistance |
| Interventions |
This study investigates whether: (i) a family history of type 2 diabetes affects exercise induced improvements in insulin sensitivity. (ii) being prediabetic affects exercise induced improvements in glycemic control. (iii) sex differences affect exercise induced improvements in glycemic control.
NCT03152669 — The Extended Salford Lung Study (“Ex-SLS”) Data Access Project
| Status | Completed |
| Phase | N/A |
| Sponsor | GlaxoSmithKline |
| Enrollment | 1183 |
| Study Type | OBSERVATIONAL |
| Conditions | Asthma |
The Salford Lung Study (SLS) subjects represent a group of COPD and asthma patients whose disease is extremely well-characterised over a short time period. Subjects in the SLS originally consented for information relevant to the study to be shared with the sponsor (GSK). These data were limited to three years prior to randomisation and the twelve-month interventional treatment period. Broadened…
NCT07687251 — Impact of Primary Nursing on Nursing-sensitive Outcomes in Inpatients Units: a Multicentre Pre-Post Study
| Status | Completed |
| Phase | N/A |
| Sponsor | Università degli Studi del Piemonte Orientale Amedeo Avogadro |
| Enrollment | 1708 |
| Study Type | INTERVENTIONAL |
| Conditions | Accidental Falls; Cross Infection (Hospital-Acquired Infections); Acute Care Unit |
| Interventions |
The aim of this quasi-experimental before-after study is to evaluate whether the implementation of the Primary Nursing (PN) pattern of care improves nursing-sensitive outcomes in adult inpatients and nurse-related outcomes across hospital wards in Northern Italy.
The main questions it aims to answer are:
- What is the impact of the PN on inpatients’ nursing-sensitive outcomes, including heal…
NCT04792697 — Experimental Manipulation of Sleep and Circadian Rhythms and the Role Played on Reward Function in Teens
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Pittsburgh |
| Enrollment | 115 |
| Study Type | INTERVENTIONAL |
| Conditions | Delayed Sleep Phase Syndrome |
| Interventions | ; ; |
Adolescence is a time of heightened reward sensitivity and greater impulsivity. On top of this, many teenagers experience chronic sleep deprivation and misalignment of their circadian rhythms due to biological shifts in their sleep/wake patterns paired with early school start times. Many studies find that this increases the risk for substance use (SU). However, what impact circadian rhythm and …
NCT04258332 — CARDIA-Salt Sensitivity of Blood Pressure (SSBP)
| Status | Completed |
| Phase | N/A |
| Sponsor | Vanderbilt University Medical Center |
| Enrollment | 281 |
| Study Type | INTERVENTIONAL |
| Conditions | Salt Sensitivity of Blood Pressure; Hypertension |
| Interventions | ; |
Salt sensitivity of blood pressure (SSBP) is defined as the change in blood pressure (BP) in relation to change in salt intake. An increase in BP from low- to high-salt diet is common and associated with an increased risk of cardiovascular morbidity and mortality, even among normotensive individuals. Yet, the pathophysiology of SSBP is not well understood. The prevailing paradigm is that abnorm…
NCT05509569 — A Survey of Icatibant in Pediatric Participants With Hereditary Angioedema
| Status | Completed |
| Phase | N/A |
| Sponsor | Takeda |
| Enrollment | 32 |
| Study Type | OBSERVATIONAL |
| Conditions | Hereditary Angioedema (HAE) |
| Interventions |
This study is a survey in Japan of Icatibant subcutaneous injection 30 mg syringe used to treat children or teenagers with acute attacks of hereditary angioedema (HAE). The study sponsor will not be involved in how the participants are treated but will provide instructions on how the clinics will record what happens during the study.
The main aim of the study is to check for side effects relat…
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 …