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

NITROX

Status and phase

Withdrawn

Phase 2

Conditions

Pulmonary Hypertension

Treatments

Drug: NX1011

Study type

Interventional

Funder types

Industry

Identifiers

NCT00323024

NX1011:201

Details and patient eligibility

About

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).

Sex

All

Ages

18 to 75 years old

Volunteers

No 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- Patient who cannot be withdrawn from nitrate therapy.