Phase 1, 3-Part, Open-Label Study to Assess Safety, Tolerability and PK of Single and Multiple Doses of PUR1900 in Healthy Subjects and Crossover Study of Single Doses of PUR1900 and Sporanox in Adult Subjects With Mild to Moderate Asthma
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 58
- 试验地点
- 2
- 主要终点
- Number of participants with treatment-related Adverse Events as assessed by CTCAE v4.0
研究概览
简要总结
Phase 1, 3-part study to assess safety, tolerability and PK of single and multiple doses of itraconazole administered as a dry powder for inhalation (PUR1900) in healthy subjects (parts 1 and 2) and a 2-period crossover study of single doses of itraconazole administered as a dry powder for inhalation (PUR1900) and an oral solution (Sporanox) in adults with mild to moderate, stable asthma (part 3)
详细描述
Phase 1, multi-center, 3-part, open-label study in healthy adults (Parts 1 and 2) and adults with mild to moderate, stable asthma (Part 3).
Safety, tolerability and PK will be assessed following either single ascending (SAD) or multiple ascending (MAD) dosing of itraconazole administered as a dry powder for inhalation (PUR1900; Part 1 and Part 2, respectively). Part 1 will comprise 3 separate cohorts planned to receive single doses of 5, 10 and 25 mg itraconzaole, respectively. The study will have an interleaved design; Part 2 will comprise 2 separate cohorts planned to receive daily doses of itraconazole 10 and 20 mg per day for 14 days, respectively. Part 2, Cohort 1 will commence after a review of safety data from Part 1 Cohort 2 suggests it is safe to do so.
Part 3 is a 2-period, randomised, crossover study in adult subjects with mild to moderate stable asthma to assess the safety, tolerability and PK of single doses of itraconazole administered as a dry powder for inhalation (PUR1900) and administered as an oral solution (Sporanox® Oral Solution).
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Sequential
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 60 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Part 1 (SAD) and Part 2 (MAD):
- •Healthy males or non-pregnant, non-lactating healthy females.
- •Age 18 to 60 years
- •Screening forced expiratory volume in 1 sec (FEV1) ≥80% of the predicted value
- •Screening FEV1/forced vital capacity (FVC) >0.
- •Able to demonstrate the correct inhalation technique for use of delivery device during the study.
- •Part 3 (Asthmatic Subjects):
- •Males or non-pregnant, non-lactating females with a physician-confirmed diagnosis of asthma for at least 3 months. Asthma must be assessed by investigator as being stable for at least 4 weeks prior to screening.
- •Age 18 to 60 years
- •Subject is being treated with either inhaled corticosteroids (ICS) or inhaled corticosteroids plus long-acting beta-agonists (ICS/LABA). Only GINA STEP 2 and 3 patients will be enrolled.
- •Pre-bronchodilator, clinic measured, FEV1 ≥70% of predicted normal at screening
- •Able to perform the required spirometric testing.
- •Able to produce a sputum sample of a quality required for drug concentration assessments (a single repeat is permitted).
排除标准
- •Subjects who have received any IMP in a clinical research study within the previous 3 months prior to dosing on this study
- •Subjects who have previously received IMP in this study. Subjects who have participated in Part 1 are not permitted to participate in Part 2 or Part
- •History of any drug or alcohol abuse in the past 2 years prior to screening.
- •Current users of e-cigarettes and nicotine replacement products and those who have used these products within the last 12 months
- •Females of childbearing potential who are pregnant or lactating, or who plan to become pregnant during the study (all female subjects must have a negative pregnancy test at screening). A woman is considered of childbearing potential unless she is permanently sterile (hysterectomy, bilateral salpingectomy, bilateral oophorectomy, bilateral tubal occlusion/ligation) or is postmenopausal (had no menses for 12 months without an alternative medical cause (will be re-assessed at admission/pre-dose).
- •Positive drugs of abuse test result at screening or admission
- •Subjects with congestive heart failure or a history of congestive heart failure
- •History of severe cough or bronchospasm upon inhalation of any dry powder inhalation product
- •Subjects who are taking or have taken any herbal remedies or CYP3A4 inducers in the 28 days prior to the first IMP administration
- •Upper respiratory tract infection (excluding otitis media), fever, acute or chronic cough within 14 days of the first IMP administration, or lower respiratory tract infection within the last 3 months prior to IMP administration
- •Recent (last 4 weeks prior to IMP administration) clinically significant bacterial, viral or fungal infection that required systemic (oral or intravenous) antibiotics, antivirals or antifungals; topical treatments, other than antifungals, are allowed.
研究组 & 干预措施
Part 1 single ascending dose
Intervention: drug Itraconzaole powder: single dose of 5mg, 10mg or 25 mg Other name: PUR1900
干预措施: Itraconazole Powder (Drug)
Part 2 multiple ascending dose
Intervention: drug Itraconzaole powder: 10 mg or 20 mg daily for 14 days Other name: PUR1900
干预措施: Itraconazole Powder (Drug)
Part 3 2-period crossover single dose
Intervention: drug Itraconzaole powder: 20 mg single dose and Itraconzaole oral solution 200 mg single dose Other names: PUR1900, Sporanox
干预措施: Itraconazole Powder (Drug)
Part 3 2-period crossover single dose
Intervention: drug Itraconzaole powder: 20 mg single dose and Itraconzaole oral solution 200 mg single dose Other names: PUR1900, Sporanox
干预措施: Itraconazole 200 mg (Drug)
结局指标
主要结局
Number of participants with treatment-related Adverse Events as assessed by CTCAE v4.0
时间窗: Part 1: Baseline through Day 14, Part 2 and 3: Baseline through Day 28
Safety and tolerability will be assessed by evaluating the number of participants with treatment-related adverse events as assessed by CTCAE v4.0
次要结局
- Apparent first-order terminal elimination half-life (t1/2 ) of single dose of itraconazole(Part 1: Baseline through Day 14, Part 2 and 3: Baseline through Day 28)
- Area under the serum concentration vs time curve within the dosing interval (AUCtau) of single dose of itraconazole(Part 1: Baseline through Day 14, Part 2 and 3: Baseline through Day 28)
- Apparent volume of distribution (Vz/F) of single dose of itraconazole(Part 1: Baseline through Day 14, Part 2 and 3: Baseline through Day 28)
- Time of the maximum measured serum concentration (Tmax) of single dose of itraconazole(Part 1: Baseline through Day 14, Part 2 and 3: Baseline through Day 28)
- Apparent first-order terminal elimination rate constant calculated from a semi-log plot of the serum concentration vs time curve (Kel) of single dose of itraconazole(Part 1: Baseline through Day 14, Part 2 and 3: Baseline through Day 28)
- Area under the serum concentration vs time curve from time 0 to infinity (AUC0-inf) of single dose of itraconazole(Part 1: Baseline through Day 14, Part 2 and 3: Baseline through Day 28)
- Apparent clearance (CL/F) of single dose of itraconazole(Part 1: Baseline through Day 14, Part 2 and 3: Baseline through Day 28)