PrecISE (Precision Interventions for Severe and/or Exacerbation-Prone Asthma) Network Study
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 395
- 试验地点
- 29
- 主要终点
- The Juniper Asthma Control Questionnaire (ACQ-6)
研究概览
简要总结
The primary objective of this study is to evaluate several interventions given to participants with severe asthma. Interventions are administered in a crossover manner with 16-week treatment periods followed by 8 to 16 week washout.
详细描述
PrecISE is a clinical study sponsored by the U.S. National Heart, Lung, and Blood Institute (NHLBI) to investigate several treatments for severe asthma. PrecISE will enroll 600 adults and teenagers (ages 12 years and older) with severe asthma who have symptoms that are not well-controlled on high dose of inhaled corticosteroids including those who have frequent asthma attacks. Each person who agrees to enroll in the PrecISE study will receive several treatments for research purposes based on their type of severe asthma.
The goal of PrecISE is to understand how to treat different types of severe asthma, by using precision medicine. Precision medicine is an approach that targets treatments to defined subgroups of patients who share similar characteristics, for example, patients with a certain genetic variation or patients with high number of blood eosinophils.
Researchers from over 30 locations across the US are involved in PrecISE.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 主要目的
- Treatment
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 12 Years 至 —（Child, Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Provision of signed and dated informed consent form
- •Started willingness to comply with all study procedures and availability for the duration of the study
- •Male or female, age ≥ 12 years
- •No change in asthma medications for the past 2 months and use of medium or high dose inhaled corticosteroids (ICS) (defined by Table 1A) + an additional asthma controller/biologic (defined in Tables 1B and 1C). Participants entered into the run-in on medium dose ICS will be switched to high dose ICS. They must meet all entry criteria at the time of randomization including the criteria for uncontrolled asthma as assessed by symptoms during the two weeks prior to the randomization.
- •Baseline poor or uncontrolled asthma, defined as meeting at least one of the following:
- •FEV1 <80% predicted (for adults ≥18) or FEV1<90% (pediatric participants <18) AND with 12% bronchodilator reversibility
- •Poor symptom control - Asthma Control Questionnaire ( ACQ-6) Score ≥1.5
- •≥1 exacerbation defined as a documented burst of systemic corticosteroids (>3 days for adults and adolescents or >1 day for adolescents treated with dexamethasone) in prior year for those not receiving chronic OCS or an increase in >50% of baseline corticosteroid dose for ≥3 days in those receiving chronic OCS.
- •For patients on a biologic agent, at least one asthma exacerbation must have occurred at least 2 months after the initiation of the biologic agent. The definition of acceptable documentation for asthma exacerbations can be found in Section 6.5.
- •Evidence of asthma demonstrated by either bronchodilator reversibility or methacholine responsiveness either during the run-in or by historical evidence of either criterion if testing was performed under the same standards of the PrecISE Network at a PrecISE recruitment center. These criteria are defined as:
- •An increase in FEV1 ≥12% (and 200 ml) after up to 8 puffs of albuterol OR
- •Positive methacholine defined as PC20 ≤16 mg/ml, or PD20 ≤400 mcg/ml
- •Agreement to adhere to Lifestyle Considerations (see Section 5.4) throughout study duration
- •Owns a device compatible with the eDiary system used for CompEx, that is, an iOS 11+ device such as iPhone, iPad or iPod, or a smartphone or tablet running on Android 5.0+
排除标准
- •Current participation in an interventional trial (e.g. drugs, diets, etc.)
- •Enrollment in a clinical trial where the study medication was administered within the past 60 days or within 5 half-lives (whichever is greater)
- •Physician diagnosis of other chronic pulmonary disorders associated with asthma-like symptoms, including, but not limited to, cystic fibrosis (CF), chronic obstructive pulmonary disease (COPD), chronic bronchitis, emphysema, severe scoliosis or chest wall deformities that affect lung function, or congenital disorders of the lungs or airways
- •Receiving one or more immune-modulating therapies for diseases other than asthma
- •Receiving methotrexate, mycophenolate (CellCept®), or azathioprine (Imuran®)
- •Receiving aero allergen immunotherapy and not on at least 3 months of maintenance allergen immunotherapy
- •Underwent a bronchial thermoplasty within the last two years
- •Born before 35 weeks of gestation
- •Uncontrolled hypertension, defined as systolic blood pressure >160 mm/Hg, or diastolic blood pressure >100 mm/Hg
- •History of malignancy except non-melanoma skin cancer within the last five years
- •History of smoking
- •If <30 years old: Smoked for ≥5 pack-years*
- •Can still be enrolled if <30, smoked <5 5 pack years and none in past year, and normal (negative) urine cotinine
- •If 30-39 years old: Smoked for ≥10 pack years
- •Can still be enrolled if ≥30, smoked <10 pack years and none in past year, provided participant demonstrates a normal (negative) urine cotinine
- •If ≥40 years old: Smoked ≥15 pack years
- •Can still be enrolled if ≥40 years old, smoked <15 pack years and none in the last year, provided participant demonstrates normal (negative) urine cotinine. Patients with a smoking history of ≥10 to <15 pack years will also need to demonstrate a normal Diffusing Capacity for Carbon Monoxide (DLCO) (>70% predicted) * Smoking equivalent pack years. One pack of cigarettes a day for 1 year is equivalent to:
- •1 cigar or pipe per day for 1 year
- •Smoked hookah or shisha =1 session per day for 1 year
- •Vaped e-cigarettes =0.5 mLs e-liquid per day for 1 year, or =1 cartridge/tank/pod per day for 1 year
- •1 use of marijuana per day for 1 year
- •Active use of any inhalant >1 time per month in the past year
- •Active smoking of conventional tobacco, inhaling of marijuana or other drugs, or vaping of e-cigarettes or vape pods >1 time per month in the past year
- •Any form of tobacco qualifies, such as: 1 cigarette, 1 hookah or shisha sessions, 1 cigar, 1 pipe, etc.
- •Any electronic (e)-device included: e-cigarette e-cig, mod, vape pen, JUUL vaping device, e-cigar, e-hookah, e-pipe, vape pods, etc.
- •Any form of inhaled marijuana, including smoking marijuana leaves or inhaling THC (tetrahydrocannabinol) via e-cigarette or device
- •Substance abuse within the last year
- •Unwillingness to practice medically acceptable birth control or complete abstinence during the study, current pregnancy, or lactation. Medically acceptable birth control/abstinence is defined as:
- •Career, lifestyle, or sexual orientation precludes intercourse with a male partner
- •For those in a monogamous relationship that precludes sexual activity with other partners, one of the sexual partners has been sterilized by vasectomy (in males) or hysterectomy and/or bilateral salpingo-oophorectomy (in females)
- •Use of highly effective methods of birth control defined as those, alone or in combination, that result in a low failure rate (i.e. less than 1% per year) when used consistently and correctly. Contraception should be used for at least 1 month prior to screening, throughout study participation and for an additional 16 weeks after the end of the final test treatment.
- •Pregnancy tests will be given to each female participant prior to study enrollment and at each clinic visit
- •Each male participant will agree to inform his sexual partner(s) of the potential for harm to an unborn child. If a sexual partner becomes pregnant while he is participating in the study, he will notify study staff within 24 hours of receiving medical confirmation. His partner will be advised to promptly notify her doctor
- •Any pregnancy (of a participant or a partner) will be monitored for adverse events with respect to pregnancy outcome until one month after birth.
- •Requirement for daily systemic corticosteroids above 10 mg of prednisone (or equivalent) per day for the past 2 months
- •Respiratory infection within 1 month of screening
- •Intubation for asthma in the last 12 months
- •Use of warfarin, current or last 30 days
- •Any clinically significant abnormal findings in the history, physical examination, vital signs, electrocardiogram, hematology or clinical chemistry during run-in period, which in the opinion of the site investigator, may put the participant at risk because of his/her participation in the study, or may influence the results of the study, or the participant's ability to complete the entire duration of the study
- •Additional exclusions for specific interventions (and not for others) are listed in the Appendices I-VI, Section 5.2
- •Safety Exclusion Criteria:
- •Participants who meet the following criteria will be excluded from the study:
- •Hemoglobin <10 g/dL
- •Absolute Neutrophil Count (ANC) <1000/µl for black participants, <1500/µl for other participants
- •Lymphocytes <500/µl
- •Platelet count <100,000/µl
- •Alanine Transaminase (ALT)/Aspartate Aminotransferase (AST) >2x upper limits of normal (ULN)
- •Bilirubin ≥2x ULN
- •Estimated glomerular filtration rate (eGFR) <60 ml/min/1.73 sq m
- •Positive Human Immunodeficiency Virus, Types 1 & 2 (HIV 1&2) Ab/Ag immunoassay followed by a confirmatory positive test (Geenius™ HIV-1/HIV-2 antibody differentiation immunoassay)
- 另有 14 项未显示
研究组 & 干预措施
Medium Chain Triglycerides (MCT)
Participants in this arm will receive Medium Chain Triglycerides (MCT) powder packets (10 g each) at each treatment visit at any point in the study. Participants will mix 1-2 packets of MCT supplement powder into liquids or semi-solid food and ingest 3 times a day during the 16-week treatment period. Participants will be randomized to the treatment sequence and will receive either the active MCT or the matching placebo first or vice versa.
干预措施: MCT (Drug)
Medium Chain Triglycerides (MCT)
Participants in this arm will receive Medium Chain Triglycerides (MCT) powder packets (10 g each) at each treatment visit at any point in the study. Participants will mix 1-2 packets of MCT supplement powder into liquids or semi-solid food and ingest 3 times a day during the 16-week treatment period. Participants will be randomized to the treatment sequence and will receive either the active MCT or the matching placebo first or vice versa.
干预措施: Placebo (Other)
Clazakizumab
Participants randomized to this arm will receive a 12.5 mg dose of Clazakizumab via a subcutaneous injection at every study visit, every 4 weeks, during the 16-week treatment period at any point in the study. Participants will be randomized to the treatment sequence and will receive either the active Clazakizumab or the matching placebo first or vice versa.
干预措施: Clazakizumab (Drug)
Clazakizumab
Participants randomized to this arm will receive a 12.5 mg dose of Clazakizumab via a subcutaneous injection at every study visit, every 4 weeks, during the 16-week treatment period at any point in the study. Participants will be randomized to the treatment sequence and will receive either the active Clazakizumab or the matching placebo first or vice versa.
干预措施: Placebo (Other)
Broncho-Vaxom
Participants randomized to this arm will receive 7 mg of Broncho-Vaxom once a day on an empty stomach for the 16-week treatment period duration at any point in the study. Participants will be randomized to the treatment sequence and will receive either the active Broncho-Vaxom or the matching placebo first or vice versa.
干预措施: Broncho-Vaxom (Drug)
Broncho-Vaxom
Participants randomized to this arm will receive 7 mg of Broncho-Vaxom once a day on an empty stomach for the 16-week treatment period duration at any point in the study. Participants will be randomized to the treatment sequence and will receive either the active Broncho-Vaxom or the matching placebo first or vice versa.
干预措施: Placebo (Other)
Imatinib
At any point in the study, participants randomized to this arm will take two 100 mg Imatinib tablets orally once a day with a meal and an 8 oz glass of water for 2 weeks. Participants will then take four 100 mg tablets once a day with a meal and an 8 oz glass of water for 14 weeks. Participants will be randomized to the treatment sequence and will receive either the active Imatinib or the matching placebo first or vice versa.
干预措施: Imatinib Mesylate (Drug)
Imatinib
At any point in the study, participants randomized to this arm will take two 100 mg Imatinib tablets orally once a day with a meal and an 8 oz glass of water for 2 weeks. Participants will then take four 100 mg tablets once a day with a meal and an 8 oz glass of water for 14 weeks. Participants will be randomized to the treatment sequence and will receive either the active Imatinib or the matching placebo first or vice versa.
干预措施: Placebo (Other)
Cavosonstat
Participants randomized to this arm will take one 50 mg Cavosonstat capsule orally twice a day for the 16-week treatment period duration at any point in the study. Participants will be randomized to the treatment sequence and will receive either the active Cavosonstat or the matching placebo first or vice versa.
干预措施: Cavosonstat (Drug)
Cavosonstat
Participants randomized to this arm will take one 50 mg Cavosonstat capsule orally twice a day for the 16-week treatment period duration at any point in the study. Participants will be randomized to the treatment sequence and will receive either the active Cavosonstat or the matching placebo first or vice versa.
干预措施: Placebo (Other)
结局指标
主要结局
The Juniper Asthma Control Questionnaire (ACQ-6)
时间窗: Measured at 16 weeks after the start of treatment.
Asthma symptom control is assessed via ACQ-6, the average score of these six items (range 0-6). The seven-point response scale: 0 = 'totally controlled' and 6 = 'severely uncontrolled'. Negative change from baseline values indicate improved asthma control. Efficacy analyses will compare the end-of-period outcome values between test treatment and placebo.
CompEx events
时间窗: Assessed over 16 weeks of treatment
CompEx is a composite outcome specific to asthma that combines clinically-relevant deteriorations captured by diary events with exacerbations. CompEx events include exacerbations and deterioration events defined based on daily recordings of peak expiratory flow (PEF) morning/evening (L/min), reliever use morning/evening (doses), symptoms morning/evening (score 0-3) from twice-daily recordings. Participants will be asked to describe their morning and symptoms using the following scale: 0-No symptoms to report, 3-I could not sleep because of my asthma/I could not perform my normal activities because of my asthma.
Forced Expiratory Volume in one second (FEV1) percent predicted
时间窗: Measured at 16 weeks after the start of treatment.
Assessed prior to bronchodilator administration. Efficacy analyses will compare the end-of-period outcome values between test treatment and placebo.
次要结局
- Symptom free days(Assessed over 16 weeks of treatment)
- Asthma free days(Assessed over 16 weeks of treatment)
- Forced Vital Capacity (FVC) pre-bronchodilation(Measured at 16 weeks after the start of treatment.)
- Time to first exacerbation(Assessed over 16 weeks of treatment)
- FEV1 post-bronchodilation(Measured at 16 weeks after the start of treatment.)
- Healthcare utilization(Assessed over 16 weeks of treatment)