3 Part Study to Assess Inhaled Nitric Oxide on Functional Pulmonary Imaging in Subj. Pulmonary Hypertension Associated w/ COPD and IPF

Chronic Obstructive Pulmonary Disease Clinical Trial

Official title:

An Exploratory, 3-Part, Clinical Study to Assess the Effect of Pulsed, Inhaled Nitric Oxide (iNO) on Functional Pulmonary Imaging Parameters in Subjects With World Health Organization (WHO) Group 3 Pulmonary Hypertension (PH) Associated With Chronic Obstructive Pulmonary Disease (COPD) on Long-Term Oxygen Therapy (LTOT) (Part 1) and in Subjects With WHO Group 3 PH Associated With Idiopathic Pulmonary Fibrosis (IPF) on LTOT (Part 2 and Part 3)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02267655
• Other study ID #: IK-7002-COPD-006
• Status: Completed
• Phase: Phase 1
• Start date: May 2015
• Est. completion date: June 28, 2017

Study information

• Verified date: August 2017
• Source: Bellerophon
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The objective of this exploratory study is to examine the utility of high resolution computed tomography (HRCT) to measure changes in functional pulmonary imaging parameters as a function of short term a) iNO administration and b) nitric oxide (NO) cylinder concentration using the investigational medical device INOpulse® DS-C in subjects with WHO Group 3 PH associated with COPD on LTOT (Part 1) and in Subjects with WHO Group 3 PH associated with Idiopathic Pulmonary Fibrosis (IPF) on LTOT (Part 2 and Part 3)

Description:

This is an exploratory, two-part, clinical study to evaluate the utility of HRCT to measure the pharmacodynamic effects of short term, pulsed administration of iNO using the combination product, inhaled nitric oxide/INOpulse in subjects with PH associated with COPD on LTOT. The utility of HRCT to characterize the effect of iNO on pulmonary imaging parameters as a function of a) short term inhaled iNO administration and b) NO cylinder concentration will be studied. In this study, pulmonary hypertension (PH) is defined as a tricuspid regurgitation velocity (TRV) ≥ 2.9 meters/second (m/s) or sPAP ≥ 38 mmHg by 2-D echocardiogram with Doppler or a mean pulmonary arterial pressure (mPAP) ≥ 25 mmHg by right heart catheterization.

Eleven subjects will be enrolled; the first 6 subjects enrolled will be assigned to Part 1, the next 2 subjects enrolled will be assigned to Part 2. After Part 1 has been completed and the results reviewed by the Sponsor, the next 4 subjects will be enrolled in Part 2. The Next three subjects will be participating in Part 3.

In Part 1, six (6) subjects with adequate kidney function will be randomized to receive the 30 mcg/kg IBW/hr doses of iNO using a cylinder concentration of 4880 ppm (6.0 mg/L).

The 2 subjects enrolled in Part 2a will be randomly assigned to 1 of 2 sequences (2 subjects/sequence) to receive iNO utilizing NO cylinder concentration (4880 ppm) at a dose of 75 mcg/kg IBW/hr or Placebo set at a dose of 75 mcg/kg IBW/hr . The 2 patients from Part 2a will enter Part 2b. During Part 2b patients will receive iNO utilizing NO cylinder concentration (4880 ppm) at a dose of 75 mcg/kg IBW/hr (INOpulse® setting of 75 mcg/kg IBW/hr) for 4 weeks for at least 12 hours/day.

The 3 subjects enrolled in Part 3a and 3b. Part 3a is dose titration visit, Part 3 is 4 weeks of treatment at dose identified in Paret 3a at the discretion of the Investigator. Part 3a: subjects will receive three different doses of iNO utilizing NO cylinder concentration of (4880ppm) at a dose of 5, 10 and 15 mcg/kg IBW/hr.

The 3 patients from Part 3a will enter Part 3b and will be administered open label iNO for 4 weeks/at least 12 hrs/day at the dose determined by the Investigator in Part 3a.

Subjects will be replaced if they are unable to complete all treatment visits or of evaluable HRCT data cannot be obtained.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 8
• Est. completion date: June 28, 2017
• Est. primary completion date: June 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 40 Years to 80 Years

Eligibility

Inclusion Criteria:

• Subjects must meet all of the following inclusion criteria to be enrolled and eligible to participate in the study:

1. A confirmed diagnosis of COPD by the Global initiative for chronic Obstructive Lung Disease (GOLD) criteria

2. Pulmonary hypertension determined by one of the following within the past 12 months:

1. A right heart catheterization (not obtained within ± 7 days of an exacerbation) with an mPAP = 25 mmHg, or

2. An echocardiogram (not obtained within ± 7 days of an exacerbation) with a TRV = 2.9 m/s or sPAP = 38 mmHg (Note: a subject with an acceptable mPAP = 25 mmHg determined by right heart catheterization will meet this inclusion criteria even with a TRV < 2.9 m/s)

3. Current or former smokers with at least 10 pack-years of tobacco cigarette smoking before study entry

4. Age = 40 years, = 80 years

5. A post-bronchodilatory FEV1/FVC < 0.7 and a FEV1 < 60% predicted (values obtained within 6 months prior to screening can be used unless obtained within ± 7 days of an exacerbation; otherwise, the test must be performed during screening)

6. Receiving LTOT for = 3 months and = 10 hours per day as determined by history

7. Females of childbearing potential must have a negative pre-treatment urine pregnancy test

8. Signed informed consent prior to the initiation of any study mandated procedures or assessments

Exclusion Criteria:

• Subjects who meet any of the following criteria are not eligible for enrollment:

1. A diagnosis of asthma or other non-COPD respiratory disease, in the opinion of the Investigator

2. Lack of patency of nares upon physical examination

3. Experienced during the last month an exacerbation requiring:

1. start of or increase in systemic oral corticosteroid therapy and/or

2. hospitalization

4. Left ventricular dysfunction as measured by:

1. Screening echocardiographic evidence of left ventricular systolic dysfunction (left ventricular ejection fraction [LVEF] < 40%), or

2. Screening echocardiographic evidence of left ventricular diastolic dysfunction

> moderate (i.e., > Grade 2), or

3. Any history of pulmonary capillary wedge pressure (PCWP), left atrial pressure (LAP) or left ventricular end diastolic pressure (LVEDP) > 18 mmHg as measured during cardiac catheterization within the past 6 months unless documented to have resolved by a subsequent cardiac catheterization

5. Renal impairment (i.e., an estimated GFRMDRD < 60 ml/min/1.73 m2) or history of renal failure using the equation (Levey et al., 2007):

estimated GFRMDRD = 175×Scr -1.154×Age-0.203 ×1.212 (if black) ×0.742 (if female)

where Scr = Standardized serum creatinine

6. Known allergy to contrast media.

7. Clinically significant valvular heart disease that may contribute to PH, including mild or greater aortic valvular disease (aortic stenosis or regurgitation) and/or moderate or greater mitral valve disease (mitral stenosis or regurgitation), or status post mitral valve replacement

8. Use within 30 days of screening or current use of approved PH medications such as sildenafil or bosentan (use of Cialis® or Viagra® for erectile dysfunction is permitted)

9. Use of investigational drugs or devices within 30 days prior to enrollment into the study

10. Any underlying medical or psychiatric condition that, in the opinion of the Investigator, makes the subject an unsuitable candidate for the study

Related Conditions & MeSH terms

• Chronic Obstructive Pulmonary Disease
• Fibrosis
• Hypertension
• Hypertension, Pulmonary
• Idiopathic Pulmonary Fibrosis
• Lung Diseases
• Lung Diseases, Obstructive
• Pulmonary Disease, Chronic Obstructive
• Pulmonary Fibrosis
• Pulmonary Hypertension

Intervention

Drug:
• inhaled Nitric Oxide - 30 mcg/kg IBW/hr
inhaled Nitric Oxide in 30 mcg/kg IBW/hr doses Part 1
• inhaled Nitric Oxide 5,10,15 mcg/Kg IBW/hr
inhaled inhaled Nitric Oxide 5,10,15 mcg/Kg IBW/hr dose titration
• inhaled nitric oxide 75 mcg/kg IBW/hr
inhaled nitric oxide 75 mcg/kg IBW/hr -Part 2b

Locations

Country	Name	City	State
Belgium	Antwerp University Hospital	Edegem

Sponsors (1)

Lead Sponsor	Collaborator
Bellerophon

Country where clinical trial is conducted

Belgium, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change from baseline in lobar blood volume at total lung capacity (TLC) after dosing with pulsed iNO as measured by HRCT	Part 1: baseline to end of treatment (1 day); Part 2: baseline to end of treatment (treatment visit B will occur at least 5 days and not more than 30 days after treatment visit A)	up to 4 weeks
Secondary	Changes in baseline measured by HRCT after dosing with pulsed iNO in Blood vessel % and density on lobar level	Changes in baseline measured by HRCT after dosing with pulsed iNO in Blood vessel % and density on lobar level	up to 4 weeks
Secondary	Changes in baseline measured by HRCT after dosing with pulsed iNO in Total lung volume at TLC	Changes in baseline measured by HRCT after dosing with pulsed iNO in Total lung volume at TLC	up to 4 weeks
Secondary	Changes in baseline measured by HRCT after dosing with pulsed iNO in Lobar volumes at TLC	Changes in baseline measured by HRCT after dosing with pulsed iNO in Lobar volumes at TLC	up to 4 weeks
Secondary	Changes in baseline measured by HRCT after dosing with pulsed iNO in Internal airflow distribution based on lobar expansion	Changes in baseline measured by HRCT after dosing with pulsed iNO in Internal airflow distribution based on lobar expansion	up to 4 weeks
Secondary	Changes in baseline measured by HRCT after dosing with pulsed iNO in Airway volume down to generation 8-10 at TLC	Changes in baseline measured by HRCT after dosing with pulsed iNO in Airway volume down to generation 8-10 at TLC	up to 4 weeks
Secondary	Changes in baseline measured by HRCT after dosing with pulsed iNO in Computational Fluid Dynamics (CFD)-based resistance on lobar level	Changes in baseline measured by HRCT after dosing with pulsed iNO in Computational Fluid Dynamics (CFD)-based resistance on lobar level	up to 4 weeks
Secondary	Changes in baseline measured by HRCT after dosing with pulsed iNO in Ventilation/perfusion (V/Q) matching	Changes in baseline measured by HRCT after dosing with pulsed iNO in Ventilation/perfusion (V/Q) matching	up to 4 weeks