EUCTR2019-003261-18-DK进行中（未招募）1 期
The effects of allergen immunotherapy on anti-viral immunity in patients with allergic asthma - VITA
未提供0 个研究点目标入组 40 人开始时间: 2019年9月12日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 入组人数
- 40
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •Written informed consent
- •Age >18 through < 70, inclusive at the time of V1
- •A historic verified diagnosis of asthma as defined by ³1 positive of following tests:
- •Reversibility to ß2-agonist
- •Positive mannitol challenge test
- •Positive methacholine test
- •Positive peak-flow variation test
- •Positive eucapnic voluntary hyperventilation test
- •Exercise test
- •Symptoms of HDM induced rhinitis and/or conjunctivitis
- •³1 self-reported worsening of asthma symptoms in relations to viral infection within last 12 months
- •³1 present or historical marker of Th2 asthma:
- •FeNO > 25 ppb at V0
- •Blood eosinophils > 0,3 x 109/L
- •Sputum eosinophils > 3%
- •A FEV1value of = 70% at V0
- •ACQ-6 > 1 (partly controlled) at V0
- •A stable asthma controller regimen with ICS (±LABA) for at least 4 weeks prior to V0
- •Sensitisation to HDM defined by =1 of following:
- •Positive skin prick test for either: Dermatophagoides pteronyssinus or Dermatophagoides farina
- •IgEHDM > 0.7 x103IU/L
- •Subjects must demonstrate acceptable inhaler and spirometry techniques during screening (as evaluated and in the opinion of study site staff)
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 35
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 5
排除标准
- •Any of the following would exclude the subject from participation in the study:
- •1. Oral corticosteroids (any dose for more than 3 days) 8 weeks prior to V1 and during run-in.
- •2. Acute upper or lower respiratory infections requiring antibiotics or antiviral medications 6 weeks prior to V0 and during run-in.
- •3. Severe oral conditions such as but not limited to:
- •Oral ulcers
- •Oral lichen planus
- •Oral mycosis
- •4. Current smokers
- •5. Any of the following concomitant allergies:
- •Birch, Cat, Dog, Horse
- •Ever in treatment with any AIT
- •7. Previous medical history or evidence of an uncontrolled intercurrent illness that in the opinion of the investigator may compromise the safety of the subject in the study or interfere with evaluation of the investigational product or reduce the subject’s ability to participate in the study. Subjects with well-controlled comorbid disease (eg, hypertension, hyperlipidaemia, gastroesophageal reflux disease) on a stable treatment regimen for 15 days prior to Visit 0 are eligible.
- •Any concomitant respiratory disease that in the opinion of the investigator and/or medical monitor will interfere with the evaluation of the investigational product or interpretation of subject safety or study results (eg, chronic obstructive pulmonary disease, cystic fibrosis, pulmonary fibrosis, bronchiectasis, allergic bronchopulmonary aspergillosis, Churg-Strauss syndrome, alpha-1-antitrypsin deficiency, Wegeners granulomatosis, Sarcoidosis).
- •Any clinically relevant abnormal findings in haematology or clinical chemistry (laboratory results from Visit 1), physical examination, vital signs during the screening, which in the opinion of the investigator, may put the subject at risk because of his/her participation in the study, or may influence the results of the study, or the subject’s ability to participate in the study.
- •Evidence of active liver disease, including jaundice, alanine transaminase, bilirubin, greater than twice the upper limit of normal (laboratory results from Visit 0).
- •History of cancer:
- •a. Subjects who have had basal cell carcinoma or in situ carcinoma of the cervix are eligible to participate in the study provided that curative therapy was completed at least 12 months prior to Visit 1.
- •b. Subjects who have had other malignancies are eligible provided that curative therapy was completed at least 5 years prior to Visit 1.
- •A helminth parasitic infection diagnosed within 24 weeks of Visit 1 that has not been treated or has not responded to standard of care therapy.
- •Known history of active tuberculosis (TB). Subjectsmay be enrolled if they have ALL of the following:
- •No symptoms of TB: productive, prolonged cough (> 3 weeks); coughing up blood; fever; night sweats; unexplained appetite loss; unintentional weight loss.
- •No known exposure to a case of active TB after most recent prophylaxis (prophylaxis required only if positive).
- •No evidence of active TB on chest radiograph within 3 months prior to the first dose of investigational product.
- •Positive hepatitis B surface antigen, or hepatitis C virus antibody serology at screening, or a positive medical history for hepatitis B or C. Subjects with a history of hepatitis B vaccination without history of hepatitis B are allowed to enrol.
- •A positive human immunodeficiency virus (HIV) test at screening or subject taking antiretroviral medications, as determined by medical history and/or subject’s verbal report.
- •History of any known primary immunodeficien
研究者
相似试验
已完成
4 期
The Effect of Allergen Immunotherapy on Anti-viral Immunity in Patients With Allergic AsthmaAllergic Asthma Due to Dermatophagoides PteronyssinusNCT04100902Bispebjerg Hospital39
已完成
不适用
on-interventional study of Allergy immunotherapy in adult patients with House dust mite allergyAsthmaHouse dust mite allergyJ30.3J45Other allergic rhinitisDRKS00009983ALK-Abelló Arzneimittel GmbH1,525
已完成
不适用
The efficacy of the combination of allergen vaccination and vitamin D3 in the reduction of allergen-specific nasal responses. A placebo controlled trial.RespiratoryVasomotor and allergic rhinitisRhinitisISRCTN42318360Academic Medical Centre (AMC) (Netherlands)90
招募中
3 期
Comparison of immunotherapy with aeroallergens and drug treatment in patients with allergic rhinitisAllergic rhinitis.Allergic rhinitis, unspecifiedJ30.9IRCT20171030037093N15Shahre-kord University of Medical Sciences120
已完成
不适用
Effect of antiviral therapy in patients with acute respiratory distress syndrome after CAP (community acquired pneumonia) and H1N1 infection on health-related quality of life (HRQoL) and cognitive performanceacute respiratory distress syndromeJ80Adult respiratory distress syndromeDRKS00011913Charité Universitätsmedizin Berlin Klinik für Anästhesiologie m. S. Intensivmedizin Campus Benjamin Franklin42