Evaluate the Safety of MN-221 in Subjects With Stable Moderate to Severe Chronic Obstructive Pulmonary Disease (COPD)

NCT ID: NCT01013142

Last Updated: 2015-05-13

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 48 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2009-11-30
• Study Completion Date: 2010-03-31

Brief Summary

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.

Detailed Description

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.

Conditions

Chronic Obstructive Pulmonary Disease

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

MN-221

Group Type: EXPERIMENTAL

MN-221 (Dose Group 1)

Intervention Type: DRUG

i.v. infusion of MN-221 (300 mcg) or placebo over 1 hour

MN-221 (Dose Group 2)

Intervention Type: DRUG

i.v. infusion of MN-221 (600 mcg) or placebo over 1 hour

MN-221 (Dose Group 3)

Intervention Type: DRUG

i.v. infusion of MN-221 (1,200 mcg) or placebo over 1 hour

MN-221 Placebo

Group Type: PLACEBO_COMPARATOR

MN-221 (Dose Group 1)

Intervention Type: DRUG

i.v. infusion of MN-221 (300 mcg) or placebo over 1 hour

MN-221 (Dose Group 2)

Intervention Type: DRUG

i.v. infusion of MN-221 (600 mcg) or placebo over 1 hour

MN-221 (Dose Group 3)

Intervention Type: DRUG

i.v. infusion of MN-221 (1,200 mcg) or placebo over 1 hour

Interventions

MN-221 (Dose Group 1)

i.v. infusion of MN-221 (300 mcg) or placebo over 1 hour

Intervention Type: DRUG

MN-221 (Dose Group 2)

i.v. infusion of MN-221 (600 mcg) or placebo over 1 hour

Intervention Type: DRUG

MN-221 (Dose Group 3)

i.v. infusion of MN-221 (1,200 mcg) or placebo over 1 hour

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Male or female 40-65 years of age, inclusive;

2. History of physician-diagnosed COPD treated for ≥ 3 months ;

3. FEV1 ≥ 30% < 80% and FEV1/FVC ratio < 0.7 at screening;

4. An increase in FEV1 of at least 12%, over the pre-albuterol FEV1 within 30 minutes after inhalation of albuterol;

5. 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);

6. Negative urine drug screen for cocaine, PCP, methamphetamine;

7. ECG with no evidence of ischemic heart disease or dysrhythmias and otherwise normal or with findings considered not clinically significant at screening;

8. QTcB and QTcF < 450 msec;

9. No clinical evidence of active ischemic heart disease as determined by the Investigator; and

10. Legally effective written informed consent obtained prior to starting any study procedures.

Exclusion Criteria

1. Beta agonist and/or anticholinergic via inhaler or intravenously ≤ 6 hours of screening;

2. Sustained release methylxanthine (e.g. Theophylline) or long acting beta agonists ≤ 24 hours prior to screening;

3. A diagnosis of clinically significant myocardial or valvular disease; including cardiomyopathy, congestive heart failure, or pulmonary edema;

4. Acute exacerbation of COPD requiring emergency treatment ≤ 30 days of screening or hospitalization ≤ 90 days of screening;

5. Antibiotic therapy for respiratory infection ≤ 30 days of screening;

6. Presence of active respiratory disease such as pneumonia, or acute bronchitis;

7. History or presence of tachyarrhythmias, with the exception of sinus tachycardia;

8. Hypokalemia defined as a potassium level ≤ 3.0 mmol/L at screening;

9. Significant renal, hepatic, endocrine, metabolic, neurologic or other systemic disease;

10. Uncontrolled hypertension defined as a blood pressure ≥ 170/100 mm Hg at screening;

11. Pregnant or lactating females;

12. Participation in another clinical study with an investigational drug within 30 days of screening;

13. A known allergy to excipients of the MN-221 drug product;

14. A known allergy to other beta agonists;

15. Previous exposure to MN-221; or

16. Use of beta blockers, MAO inhibitors, or tricyclic antidepressants ≤ 2 weeks prior to screening.

• Minimum Eligible Age: 40 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

MediciNova

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Alan W Dunton, MD

Role: STUDY_DIRECTOR

MediciNova

Locations

Dedicated Phase I

Phoenix, Arizona, United States

California Research Medical Group, INC

Fullerton, California, United States

Vita Research Solutions & Medical Center, Inc.

Tamarac, Florida, United States

Florida Pulmonary Research Institue, LLC

Winter Park, Florida, United States

Vince and Associates Clinical Research

Overland Park, Kansas, United States

Gulf Coast Research, LLC

Lafayette, Louisiana, United States

SNBL CLinical Pharmacology Center

Baltimore, Maryland, United States

Countries

United States

Other Identifiers

MN-221-CL-010

Identifier Type: -

Identifier Source: org_study_id