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Dose Determination Safety and Activity Study of Inhaled NX1011 to Treat Pulmonary Arterial Hypertension

Primary Purpose

Pulmonary Hypertension

Status
Withdrawn
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
NX1011
Sponsored by
NITROX, LLC
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pulmonary Hypertension focused on measuring Pulmonary Arterial Hypertension, Pulmonary Hypertension, Idiopathic PAH, PH associated with connective tissue disease (CTD), PH associated with interstitial lung disease (ILD), PH associated with congestive heart failure (CHF), PH associated with chronic obstructive pulmonary disease (COPD)

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Patient must either: meet the PAH diagnostic criteria at Screening (based on a documented history of diagnosis as outlined in the American College of Chest Physicians [ACCP] 2004 Evidence-Based Clinical Practices Guidelines)15; or have elevated pulmonary pressure with a suspected PAH diagnosis based on a clinical referral at Screening for a RHC. Patient must have PAH as defined by a mean pulmonary artery pressure (PAP) > 25 mmHg. Patient must have symptoms of pulmonary hypertension (PH) according to the World Health Organization (WHO) Functional Classification of Pulmonary Hypertension Class II through IV. Patient must consent to, be able to tolerate, and have adequate venous and arterial access for Swan-Ganz catheterization (SGC) and an arterial line. Exclusion Criteria: Clinically significant right-to-left intracardiac shunts based on Doppler echocardiography with bubble study. History of pulmonary veno-occlusive disease or clinically significant aortic or mitral stenosis. History of sustained ventricular tachycardia (VT-S) or ventricular fibrillation (VF) and cardiac arrest, or presence of atrial fibrillation. Active cardiac disease meeting the following criteria: Patient with elevated pulmonary capillary wedge pressures (PCWPs) > 25 mmHg. Patient with a history of myocardial infarction or coronary intervention within the last 60 days. Patient with a history of pacemaker, cardiac defibrillator, or biventricular pacemaker insertion within 4 weeks of Baseline. Patient who cannot be withdrawn from nitrate therapy.

Sites / Locations

  • Arizona Pulmonary Specialists, Ltd.
  • University of California, San Diego Medical Center
  • Christiana Care Health Services
  • University of Maryland
  • Brigham and Women's Hospital
  • University of Michigan Medical Center

Outcomes

Primary Outcome Measures

To evaluate the safety, tolerability, and activity of inhalation therapy with NX1011 based on right heart catheterization (RHC) measures, pulse oximetry, and hemodynamic response
To establish maximum tolerated dose (MTD) levels of NX1011 based on predefined criteria for dose-limiting toxicity (DLT)
To qualify the delivery apparatus
To generate descriptive data on the concentration-response relationship in order to choose a range of concentrations (e.g., low, medium, high) for the follow-up, fixed-dose, placebo-controlled study
To summarize correlation data between echocardiography and RHC measures with respect to activity and methemoglobin levels documented via the visible light spectroscopy

Secondary Outcome Measures

To summarize correlation data between echocardiography and RHC measures with respect to activity and methemoglobin levels documented via the visible light spectroscopy

Full Information

First Posted
May 5, 2006
Last Updated
August 29, 2007
Sponsor
NITROX, LLC
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1. Study Identification

Unique Protocol Identification Number
NCT00323024
Brief Title
Dose Determination Safety and Activity Study of Inhaled NX1011 to Treat Pulmonary Arterial Hypertension
Official Title
An Open-Label, Dose-Determination Safety, Tolerability, and Activity Study of Inhaled NX1011 in Patients With Pulmonary Arterial Hypertension
Study Type
Interventional

2. Study Status

Record Verification Date
July 2006
Overall Recruitment Status
Withdrawn
Study Start Date
September 2006 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
May 2007 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
NITROX, LLC

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to determine the safety and maximum tolerated dose of inhaled NX1011 for the treatment of pulmonary arterial hypertension (PAH).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pulmonary Hypertension
Keywords
Pulmonary Arterial Hypertension, Pulmonary Hypertension, Idiopathic PAH, PH associated with connective tissue disease (CTD), PH associated with interstitial lung disease (ILD), PH associated with congestive heart failure (CHF), PH associated with chronic obstructive pulmonary disease (COPD)

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
72 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
NX1011
Primary Outcome Measure Information:
Title
To evaluate the safety, tolerability, and activity of inhalation therapy with NX1011 based on right heart catheterization (RHC) measures, pulse oximetry, and hemodynamic response
Title
To establish maximum tolerated dose (MTD) levels of NX1011 based on predefined criteria for dose-limiting toxicity (DLT)
Title
To qualify the delivery apparatus
Title
To generate descriptive data on the concentration-response relationship in order to choose a range of concentrations (e.g., low, medium, high) for the follow-up, fixed-dose, placebo-controlled study
Title
To summarize correlation data between echocardiography and RHC measures with respect to activity and methemoglobin levels documented via the visible light spectroscopy
Secondary Outcome Measure Information:
Title
To summarize correlation data between echocardiography and RHC measures with respect to activity and methemoglobin levels documented via the visible light spectroscopy

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient must either: meet the PAH diagnostic criteria at Screening (based on a documented history of diagnosis as outlined in the American College of Chest Physicians [ACCP] 2004 Evidence-Based Clinical Practices Guidelines)15; or have elevated pulmonary pressure with a suspected PAH diagnosis based on a clinical referral at Screening for a RHC. Patient must have PAH as defined by a mean pulmonary artery pressure (PAP) > 25 mmHg. Patient must have symptoms of pulmonary hypertension (PH) according to the World Health Organization (WHO) Functional Classification of Pulmonary Hypertension Class II through IV. Patient must consent to, be able to tolerate, and have adequate venous and arterial access for Swan-Ganz catheterization (SGC) and an arterial line. Exclusion Criteria: Clinically significant right-to-left intracardiac shunts based on Doppler echocardiography with bubble study. History of pulmonary veno-occlusive disease or clinically significant aortic or mitral stenosis. History of sustained ventricular tachycardia (VT-S) or ventricular fibrillation (VF) and cardiac arrest, or presence of atrial fibrillation. Active cardiac disease meeting the following criteria: Patient with elevated pulmonary capillary wedge pressures (PCWPs) > 25 mmHg. Patient with a history of myocardial infarction or coronary intervention within the last 60 days. Patient with a history of pacemaker, cardiac defibrillator, or biventricular pacemaker insertion within 4 weeks of Baseline. Patient who cannot be withdrawn from nitrate therapy.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Victoria A Christian
Organizational Affiliation
NITROX, LLC
Official's Role
Study Director
Facility Information:
Facility Name
Arizona Pulmonary Specialists, Ltd.
City
Phoenix
State/Province
Arizona
ZIP/Postal Code
85013
Country
United States
Facility Name
University of California, San Diego Medical Center
City
La Jolla
State/Province
California
ZIP/Postal Code
92037
Country
United States
Facility Name
Christiana Care Health Services
City
Newark
State/Province
Delaware
ZIP/Postal Code
19718
Country
United States
Facility Name
University of Maryland
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21201
Country
United States
Facility Name
Brigham and Women's Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States
Facility Name
University of Michigan Medical Center
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48109
Country
United States

12. IPD Sharing Statement

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Dose Determination Safety and Activity Study of Inhaled NX1011 to Treat Pulmonary Arterial Hypertension

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