- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT02059434
Two-part Pharmacokinetic and Pharmacodynamic Study of LAS190792 in Patients With Asthma and COPD
A 2-Part, Randomised, Placebo-Controlled, Safety, Tolerability, Pharmacokinetic And Pharmacodynamic Study Of LAS190792 Delivered By Inhalation In Asthmatic And Chronic Obstructive Pulmonary Disease (COPD) Subjects
연구 개요
상태
상세 설명
This study is an integrated Phase I protocol divided into 2 parts.
Part one: a single ascending dose study (6 LAS190792 dose levels) in 16 male subjects with mild asthma. LAS190792 will be administered (by the Genuair® inhaler) under supervision at the study centre, according to the randomisation scheme. One dose level will be administered per week with 2 to 3 weeks between each dose level for the safety and pharmacokinetic data review.
Part two: A 5-way , crossover, single dose study (of LAS190792 [two doses], indacaterol, tiotropium and placebo) in 40 male and non-childbearing potential women subjects with moderate to severe COPD. Each treatment period will be separated by a washout period of at least 7 to 14 days. The aim is to ensure at least 30 subjects complete Part 2 of the study. The primary comparison for bronchodilation will be between LAS190792 doses and placebo. Other treatment comparisons (indacaterol or tiotropium vs placebo and LAS190792 vs indacaterol or tiotropium) will be considered additional.
연구 유형
등록 (실제)
단계
- 1단계
연락처 및 위치
연구 장소
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London, 영국, SE1 1YR
- Quintiles Drug Research Unit at Guy's Hospital
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Manchester, 영국, M23 9QZ
- Medicines Evaluation Unit Ltd (MEU)
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria (PART 1):
- Adult male subjects aged 18 to 70 years
- Body mass index (BMI) 18.5 to 30 kg/m2 at screening
- Clinical diagnosis of mild persistent asthma (according to GINA guidelines) for at least 6 months prior to screening
- Ability to change current asthma therapy, to discontinue previous prescribed medications after signature of informed consent as per required washout periods
- Screening FEV1 value of ≥70% of the predicted normal value after a washout of at least 5 h for short-acting beta2-agonists and 72 h for long-acting beta2-agonists
- FEV1 reversibility of ≥12% and an absolute increase of at least 200 mL over the baseline value within 30 min after inhalation of 400 µg of salbutamol
- Subjects using intermittent salbutamol and / or subjects on a stable dose or regimen of low dose ICS (as defined by the GINA guidelines) at least 4 weeks prior to screening
- Predose FEV1 value of first treatment period within the range of ±20% of the FEV1 measured at screening prior to salbutamol inhalation
- Subjects who are otherwise healthy as determined by medical history, physical examination, 12-lead ECG findings
- Normal blood pressure (defined as SBP between 100 and 140 mmHg, and DBP between 50 and 90 mmHg) at screening, measured after resting in supine position for 5 minutes.
- Subjects whose clinical laboratory test results are not clinically relevant and are acceptable to the Investigator
- Subjects who are negative for hepatitis B surface antigen (HBsAg), hepatitis B core (HBc) antibody (IgM), hepatitis C antibody and human immunodeficiency virus (HIV) I and II antibodies at screening
- Subjects who are able and willing to provide written informed consent
- Subjects able to perform repeatable pulmonary function testing for FEV1 according to the American Thoracic Society (ATS) / European Respiratory Society (ERS) 2005 criteria at screening
Inclusion Criteria (PART 2):
- Adult male and non-childbearing potential women subjects aged ≥40 years with a clinical diagnosis of stable moderate to severe COPD according to GOLD guidelines at screening
- Females must be of non-childbearing potential, confirmed at screening
- Post-salbutamol FEV1 <80% and ≥30% of the predicted normal value and post-salbutamol FEV1 / forced vital capacity (FVC) <70%
- Ability to change current COPD therapy, to discontinue previous prescribed medications after signature of informed consent
- No evidence of clinically significant respiratory and / or cardiovascular conditions or laboratory abnormalities
- No other relevant pulmonary disease or history of thoracic surgery
- No contraindication to the use of anticholinergic drugs such as known symptomatic prostatic hypertrophy, bladder neck obstruction, narrow-angle glaucoma, or beta2-agonists usage
- Subjects who are negative for HBsAg, HBc IgM, hepatitis C antibody and HIV I and II antibodies at screening
- Subjects who are able and willing to provide written informed consent
- Subjects able to perform repeatable pulmonary function testing for FEV1 according to the ATS / ERS 2005 criteria at screening
Exclusion Criteria (PART 1 and 2):
- Subjects who do not conform to the above inclusion criteria
- Current smokers, subjects with a smoking history during the last 12 months or subjects with a smoking history of more than 10 pack-years
- Other relevant pulmonary disease or history of thoracic surgery
- Subjects with a BMI ≥40 kg/m2 (only applicable for Part 2)
- Subjects with any clinically relevant history or presence of abnormality from the medical history and/or physical examination (only applicable for Part 1)
- Current evidence or recent history of any clinically significant and unstable disease (other than COPD) or abnormality that could put the subject at risk or could confound the results of the study (only applicable for Part 2)
- Subjects with a surgical history clinically relevant for the purpose of the study
- History of malignancy of any organ system, treated or untreated within the past 5 years, with the exception of localised basal cell carcinoma of the skin
- Subjects with serious adverse reaction or serious hypersensitivity to Spiriva (for Part 2 only), indacaterol (for Part 2 only), or the formulation excipients (eg, lactose) or other drugs in the same pharmacologic class (for Part 1 and Part 2)
- Current diagnosis of COPD (for Part 1 only) or history of / or current diagnosis for asthma (for Part 2 only)
- Recent history of asthma / COPD exacerbation requiring hospitalisation or need for increased maintenance treatments for asthma / COPD within 6 weeks prior to screening or randomisation
- Use of daily oxygen therapy >10 h per day (for Part 2 only)
- Use of systemic steroids for respiratory reasons within 3 months prior to screening
- Lower respiratory tract infection within 6 weeks prior to screening or randomisation
- Upper respiratory tract infection requiring antibiotics within 4 weeks prior to screening or randomisation
- Current history of tuberculosis, bronchiectasis or other non-specific pulmonary disease
- QTcF interval >430 ms at screening or prior to randomisation, or history of long QT syndrome (for Part 1 only)
- QTcF interval, >450 ms for males and >470 ms for females at screening or prior to randomisation, or history of long QT syndrome (for Part 2 only)
- Subjects with a history of excessive use or abuse of alcohol or with a history of drug abuse within the past 2 years
- Subjects who are positive for drugs of abuse and alcohol tests at screening and prior to randomisation
- Donation or loss >400 ml of blood and plasma within the previous 3 months prior to screening
- Subjects consuming more than 14 (female subjects) or 21 (male subjects) units of alcohol a week
- Subjects with a significant infection or known inflammatory process at screening or prior to randomisation
- Subjects with acute gastrointestinal symptoms at the time of screening or prior to randomisation
- Subjects with an acute infection such as influenza at the time of screening or prior to randomisation
- Male subjects who do not agree to follow instructions to avoid pregnancies
- Subjects who are not able to adhere to the restrictions on prior and concomitant medications
- Subjects who intend to use any concomitant medication not permitted by the protocol or who have not undergone the required washout period for a particular prohibited medication
- Subjects who have used any investigational drug within 3 months prior to screening or within the equivalent time of 6 half-lives of receiving the last administration, whichever is longer
- Subjects who have received the last dose of investigational product more than 3 months ago but who are on an extended follow-up
- Subjects who are vegans or who have medical dietary restrictions
- Subjects unable to communicate reliably with the Investigator
- Subjects who are unlikely to co-operate with the requirements of the study
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 크로스오버 할당
- 마스킹: 하나의
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
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실험적: LAS190792 Dose 1 (Part 1)
Single dose, oral inhalation by Genuair® single-dose dry powder inhaler (DPI)
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실험적: LAS190792 Dose 2 (Part 1)
Single dose, oral inhalation by Genuair® single-dose dry powder inhaler (DPI)
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실험적: LAS190792 Dose 3 (Part 1)
Single dose, oral inhalation by Genuair® single-dose dry powder inhaler (DPI)
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실험적: LAS190792 Dose 4 (Part 1)
Single dose, oral inhalation by Genuair® single-dose dry powder inhaler (DPI)
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실험적: LAS190792 Dose 5 (Part 1)
Single dose, oral inhalation by Genuair® single-dose dry powder inhaler (DPI)
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실험적: LAS190792 Dose 6 (Part 1)
Single dose, oral inhalation by Genuair® single-dose dry powder inhaler (DPI)
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위약 비교기: Placebo (Part 1)
Single dose, oral inhalation by Genuair® single-dose dry powder inhaler (DPI)
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실험적: LAS190792 Dose 1 (Part 2)
Single dose, oral inhalation by Genuair® single-dose dry powder inhaler (DPI)
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실험적: LAS190792 Dose 2 (Part 2)
Single dose, oral inhalation by Genuair® single-dose dry powder inhaler (DPI)
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활성 비교기: Tiotropium 18 μg
Single dose, oral inhalation by HandiHaler® single-dose DPI
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다른 이름들:
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활성 비교기: Indacaterol 150 μg
Single dose, oral inhalation by Breezhaler® single-dose DPI
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다른 이름들:
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위약 비교기: Placebo (Part 2)
Single dose, oral inhalation by Genuair® single-dose dry powder inhaler (DPI)
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Subjects With ≥1 Treatment-emergent Adverse Event
기간: 30 Days
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Adverse events (AEs) are any unfavorable and unintended medical occurrence during the subject's participation in the study (including deterioration of a pre-existing medical condition, an abnormal value in a laboratory assessment, an ECG abnormality, a 12-lead 24-hour ECG-Holter abnormality, a blood pressure abnormal value, paradoxal bronchospasm or an abnormal finding in the physical examination) and will be coded using the current Medical Dictionary for Regulatory Activities (MedDRA).
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30 Days
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Change From Baseline in Trough FEV1 (Forced Expiratory Volume in 1 Second)
기간: Day 2
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Trough is defined as the mean of the FEV1 values obtained at 23 hours and at 24 hours after morning investigational product administration.
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Day 2
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2차 결과 측정
결과 측정 |
기간 |
|---|---|
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Maximum Observed Plasma Concentration (Cmax)
기간: Up to 36 hours after investigational product administration
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Up to 36 hours after investigational product administration
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Time to Maximum Observed Plasma Concentration (Tmax)
기간: Up to 36 hours after investigational product administration
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Up to 36 hours after investigational product administration
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Area Under the Concentration-time Curve From Zero to the Time of the Last Measurable Concentration
기간: Up to 36 hours after investigational product administration
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Up to 36 hours after investigational product administration
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공동 작업자 및 조사자
스폰서
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
기본 완료 (실제)
연구 완료 (실제)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (추정)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
- M-190792-01
- 2013-001758-93 (EudraCT 번호)
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