A Phase I Randomized, Double-blind, Placebo-controlled Dose Escalation Study to Evaluate the Safety and Efficacy of MN-221 When Administered Intravenously to Subjects With Stable Moderate to Severe Chronic Obstructive Pulmonary Disease (COPD)
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- MediciNova
- 入组人数
- 48
- 试验地点
- 7
- 主要终点
- Adverse events, cardiac and ECG parameters, vital signs, physical exam and clinical laboratory assessments.
研究概览
简要总结
The objective of this clinical study is to determine the safety of intravenous MN-221 compared to placebo when administered in subjects diagnosed with stable moderate to severe COPD.
详细描述
This is a randomized, double-blind, placebo-controlled, multi-center dose escalation study in subjects diagnosed with stable moderate to severe COPD. The study will be conducted in approximately 6 Clinical Research Units (CRUs).
Subjects with a diagnosis of stable moderate to severe COPD will be screened and must demonstrate an improvement in FEV1 after bronchodilator treatment of at least 12% at Screen Visit 1. The subject's degree of dyspnea will be captured on the British Medical Research Council (MRC) questionnaire, and severity will be determined by the Global Initiative for Chronic Obstructive Lung Disease (GOLD) spirometric criteria. Subjects meeting entry criteria at Screen Visit 1 will be asked to return to the CRU for Screen Visit 2 within 14 days of Visit 1. Subjects confirming entry criteria including degree of COPD severity by spirometry at Screen Visit 2 will be randomized to receive either MN-221 or placebo. Serial spirometry will be performed over the 8 hour treatment period after initiation of study drug administration. Subjects will be discharged from the CRU after completing the Hour 8 study procedures and asked to return approximately 24 hours after initiation of study drug for follow up safety assessments including spirometry. A study diary will be provided to each subject upon discharge from the CRU to complete as instructed and return it to the site at the 24 hour Follow-up Visit.
There will be three dose levels and each will include approximately 16 subjects randomized to receive either MN-221 or placebo in 3:1 ratio (12 subjects receive MN-221:4 subjects receive placebo). A risk/benefit evaluation will be performed by the study's Safety Review Committee at completion of each dose level prior to escalating to the next dose level.
Safety and efficacy will be monitored throughout the treatment period. Blood samples for PK parameters and metabolite identification will be obtained.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 40 Years 至 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Male or female 40-65 years of age, inclusive;
- •History of physician-diagnosed COPD treated for ≥ 3 months ;
- •FEV1 ≥ 30% < 80% and FEV1/FVC ratio < 0.7 at screening;
- •An increase in FEV1 of at least 12%, over the pre-albuterol FEV1 within 30 minutes after inhalation of albuterol;
- •Negative urine pregnancy test for all females unless the subject is post-menopausal (≥ 24 months of spontaneous amenorrhea) or surgically sterile (hysterectomy, bilateral ovariectomy or bilateral tubal ligation);
- •Negative urine drug screen for cocaine, PCP, methamphetamine;
- •ECG with no evidence of ischemic heart disease or dysrhythmias and otherwise normal or with findings considered not clinically significant at screening;
- •QTcB and QTcF < 450 msec;
- •No clinical evidence of active ischemic heart disease as determined by the Investigator; and
- •Legally effective written informed consent obtained prior to starting any study procedures.
排除标准
- •Beta agonist and/or anticholinergic via inhaler or intravenously ≤ 6 hours of screening;
- •Sustained release methylxanthine (e.g. Theophylline) or long acting beta agonists ≤ 24 hours prior to screening;
- •A diagnosis of clinically significant myocardial or valvular disease; including cardiomyopathy, congestive heart failure, or pulmonary edema;
- •Acute exacerbation of COPD requiring emergency treatment ≤ 30 days of screening or hospitalization ≤ 90 days of screening;
- •Antibiotic therapy for respiratory infection ≤ 30 days of screening;
- •Presence of active respiratory disease such as pneumonia, or acute bronchitis;
- •History or presence of tachyarrhythmias, with the exception of sinus tachycardia;
- •Hypokalemia defined as a potassium level ≤ 3.0 mmol/L at screening;
- •Significant renal, hepatic, endocrine, metabolic, neurologic or other systemic disease;
- •Uncontrolled hypertension defined as a blood pressure ≥ 170/100 mm Hg at screening;
- •Pregnant or lactating females;
- •Participation in another clinical study with an investigational drug within 30 days of screening;
- •A known allergy to excipients of the MN-221 drug product;
- •A known allergy to other beta agonists;
- •Previous exposure to MN-221; or
- •Use of beta blockers, MAO inhibitors, or tricyclic antidepressants ≤ 2 weeks prior to screening.
研究组 & 干预措施
MN-221 Placebo
干预措施: MN-221 (Dose Group 3) (Drug)
MN-221
干预措施: MN-221 (Dose Group 1) (Drug)
MN-221
干预措施: MN-221 (Dose Group 2) (Drug)
MN-221
干预措施: MN-221 (Dose Group 3) (Drug)
MN-221 Placebo
干预措施: MN-221 (Dose Group 1) (Drug)
MN-221 Placebo
干预措施: MN-221 (Dose Group 2) (Drug)
结局指标
主要结局
Adverse events, cardiac and ECG parameters, vital signs, physical exam and clinical laboratory assessments.
时间窗: Hour 0 (treatment) through Hour 24 (follow-up)
次要结局
- Forced expiratory volume in one second (FEV1).(Pre-dose to Hour 24 post-dose)
- Pharmacokinetic parameters of MN-221.(Pre-dose to Hour 24 post-dose)