Phase 1 PK Study of AERO-007, an Inhaled LABA+LAMA Combination for Nebulization Delivery in COPD Patients
Comparison of Pharmacokinetics of Glycopyrrolate (AERO-002) in AERO-007 Combination Product Versus Active Comparator Inhalation Glycopyrrolate Product in Healthy Volunteers
研究概览
详细说明
AERO-007 is a propriety inhalation solution formulation of fixed-dose combination of LABA+LAMA (indacaterol and glycopyrrolate) for delivery using a general-purpose nebulizer device.
Combination of a long-acting beta-agonist (LABA) bronchodilator and a long-acting muscarinic antagonist (LAMA) bronchodilator is the preferred choice for initial pharmacotherapy for COPD patients with high symptom severity, frequently experiencing breathlessness, and patients with high exacerbation risk.
Although there are currently multiple LABA+LAMA combination bronchodilators available in handheld inhalers, a significant number of COPD patients, generally high risk and older patients, do not receive optimal benefit from inhalers. Nebulized delivery provides an effective alternative where disease management is sub optimal. To date there are no approved LABA+LAMA combinations available by nebulization.
In this phase 1 study, 24 healthy volunteers will be randomized to receive single doses of two study treatments (AERO-002 and active comparator) in a crossover design administered by random sequence. Study assessments will be performed pre- and post-dose for 24 hours. Treatment visits will be separated by a washout period of 7 days.
研究类型
注册 (估计的)
阶段
- 阶段1
联系人和位置
学习联系方式
- 姓名:Ahmet Tutuncu, MD, PhD
- 电话号码:+1-858-750-4717
- 邮箱:Ahmet.Tutuncu@AeroRxTherapeutics.com
学习地点
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Manchester、英国
- Medicines Evaluation Unit Ltd
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接触:
- Dave Singh, MD
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首席研究员:
- Dave Singh, MD
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参与标准
资格标准
适合学习的年龄
- 成人
接受健康志愿者
描述
Inclusion Criteria:
- Male or female aged 18 to 55 years, inclusive, at the time of informed consent
- Forced expiratory volume in 1 second (FEV1) > 80% of predicted normal at the Screening Visit (using the Global Lung Function Initiative [GLI] 2012 reference values)
- Body mass index > 18 and < 32 kg/m2 at the Screening Visit
- Able to abstain from alcohol for 24 hours prior to the Screening Visit, and prior to and after each dosing visit
- Female participants of childbearing potential must not be pregnant, breast feeding, or lactating, and heterosexual female participants of childbearing potential must agree to use, with their partner, a male condom plus an approved method of highly effective birth control from the time of informed consent and for 30 days following the last administered dose
- Female participants of childbearing potential must have a negative serum or urine pregnancy test at the Screening Visit and a negative urine pregnancy test prior to dosing at each Treatment Visit
- Male participants who are sexually active with a female partner of childbearing potential must use, with their partner, a male condom plus an approved method of highly effective contraception from the time of informed consent and for 30 days following the last administered dose
- Participants must agree not to donate semen or ova/oocytes from the time of informed consent and for 30 days following the last administered dose
- Participants must be in good health as determined by medical history, physical examination, vital signs, 12-lead ECG, and clinical laboratory assessments at the time of screening, as judged by the Investigator
- Willing and able to provide written informed consent
Exclusion Criteria:
- Any condition or abnormality (including medical history, clinical laboratory, ECG, physical examination, or vital sign abnormalities), current or past, that, in the opinion of the Investigator or Medical Monitor, would compromise the safety of the participant, or would interfere with or complicate study procedures or assessments
- Lower respiratory tract infection within 6 weeks prior to the Screening Visit
- History of malignancy of any organ system, except for localized skin cancers, within 5 years prior to the Screening Visit
- Major surgery (requiring general anaesthesia) within 6 weeks prior to the Screening Visit, or planned surgery through the end of the study
- Positive serum hepatitis B surface antigen (HbsAg), hepatitis C virus antibodies (HCV Ab) or human immunodeficiency virus (HIV) 1 and/or 2 antibodies at the Screening Visit
- Chronic viral infection or immunodeficiency condition
- History of any drug and/or alcohol abuse in the past 2 years prior to the Screening Visit
- Current or previous use of tobacco, nicotine products, or e-cigarettes within 6 months prior to the Screening Visit through the End of Study Visit
- Smoking history of > 5 pack years
- Positive urine cotinine test at the Screening Visit or prior to dosing at each Treatment Visit
- Regular alcohol consumption in males >21 units per week and females >14 units per week
- Positive urine drugs of abuse test and/or alcohol breath test at the Screening Visit or prior to dosing at each Treatment Visit that cannot be accounted for by concomitant medication, in the opinion of the Investigator
- Donation of ≥ 450 mL of blood within 8 weeks of the Screening Visit
- History of intolerance or hypersensitivity to any of the ingredients in the formulation for AERO-002 or other aerosol medications
- Participation in another investigational drug study within 30 days of the last dose, 5 average terminal elimination half-lives (T1/2) or twice the duration of the biological effect, whichever is longer, prior to the Screening Visit
- History or high risk of noncompliance with study visits and procedures or unsuitable for entry into the study, at the discretion of the Investigator
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:交叉作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的:AERO-002
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Single dose, administered via inhalation using a standard jet nebulizer
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有源比较器:Glycopyrrolate pMDI
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Single dose, administered via inhalation using pMDI
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Pharmacokinetics - AUC
大体时间:0 to 24 hours post-dose
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AUC0-t (area under the plasma concentration from time 0 to the last collection time)
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0 to 24 hours post-dose
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|
Pharmacokinetics - Cmax
大体时间:0 to 24 hours post-dose
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Cmax (maximum plasma concentration)
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0 to 24 hours post-dose
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Adverse events
大体时间:From the first dose to the end of the study visit at Day 7
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Treatment-emergent AEs
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From the first dose to the end of the study visit at Day 7
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合作者和调查者
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- AERO-007-03
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
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