Study to Assess Acute Vasodilation Response of Inhaled Nitric Oxide

Pulmonary Arterial Hypertension Clinical Trial

— EAGLE  

Official title:

A Phase 3 Open-label Multi-Center, Two-Part Single-arm Study to Evaluate the Acute Vasodilation Response of Inhaled Nitric Oxide as a Predictor of Successful Wean From Parental Prostacyclins in Subjects With Pulmonary Arterial Hypertension

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT02436512
• Other study ID #: P-2014-001
• Status: Withdrawn
• Phase: Phase 3
• First received: April 13, 2015
• Last updated: September 3, 2015
• Start date: June 2015
• Est. completion date: August 2015

Study information

• Verified date: June 2015
• Source: Geno LLC
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

The EAGLE study is a Phase 3, open-label, multi-center, two-part, single-arm study of GeNOsyl(R) delivery system(s) to evaluate if inhaled nitric oxide-induced vasodilation predicts successful wean from parenteral prostacyclin (PGI) in subjects with World Health Organization (WHO) Group 1 pulmonary arterial hypertension (PAH) undergoing a medically necessary right heart catheterization (RHC). All subjects enrolled in the study will undergo an attempt to wean from parenteral PGI per standard of care.

Description:

This study will be divided into 2 parts: a Pilot Phase followed by Pivotal Phase.

• The Pilot Phase will enroll up to 20 subjects. The information derived from the Pilot Phase will evaluate safety, and assess the vasoreactivity test response rate.

• Approximately 150 subjects will be enrolled in the Pivotal Phase of the study, to gather further data on weaned successes from parenteral PGI. The Investigator and study staff involved with the wean and patient management will be blinded in this phase of the study to the vasoreactivity results.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: August 2015
• Est. primary completion date: August 2015
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

• The subject or subject's legally authorized representative signs and dates an Institutional Review Board (IRB) approved informed consent form prior to the initiation of any study-related activities.

• The subject has been diagnosed with PAH (WHO Group 1) and is WHO Functional Class I or II at Screening.

• The subject has documented continuous PGI use for = 1 year from Screening, without a significant interruption (i.e., = 2 day interruption) and without a failed complete wean attempt.

• The subject is a candidate for weaning off parenteral PGI therapy (per Investigator judgment and standard of care).

Exclusion Criteria

• The subject has a hypersensitivity or allergy to ingredients of inhaled nitric oxide or other clinically significant allergies (clinical significance per Investigator judgment).

• The subject has a PCWP or left ventricular end diastolic pressure (LVEDP) =15 mmHg at Baseline.

• The subject has participated in an investigational product or device study within the 30 days prior to Screening.

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic

Related Conditions & MeSH terms

• Hypertension
• Pulmonary Arterial Hypertension

Intervention

Drug:
• Inhaled Nitric Oxide
The investigational product is inhaled nitric oxide delivered via nasal cannula or venturi mask with the GeNOsylTM Delivery System or GeNOsylTM Acute DS, during RHC as follows: (Dose 1): 5 ppm inhaled nitric oxide for 15 minutes (Dose 2): 40 ppm inhaled nitric oxide for 15 minutes

Locations

Country	Name	City	State
United States	University of Alabama	Birmingham	Alabama
United States	Allegheny General Hospital	Pittsburgh	Pennsylvania

Sponsors (1)

Lead Sponsor	Collaborator
Geno LLC

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Wean Success vs Wean Failure	To evaluate the number of subjects that achieve Wean Success that are Vasoreactivity Response (VR) positive (+) versus VR negative (-)and the number of subjects that are Wean Failures that are VR(+) versus VR(-).; Wean-Success: No parenteral PGI therapy at 3 months post-wean completion; and; Clinical stability, where clinical stability is defined as: A decrease in 6MWT distance less than 10% from pre-wean; and; NT-proBNP increase <15% from pre-wean; and; WHO Functional Class Wean-Failure: Subjects that wean successfully but do not meet all clinical stability components of the Wean-Success definition above; or; Failure to wean within the 3 month Transition Period; or; Re-initiation of parental PGI during the 3 month post-wean or subject does not meet the definition of clinical stability at 3 month post-wean; or; Death or hospitalization due to progression of disease; or; Atrial septostomy; or; Heart and/or lung transplantation	Visit 4 - Day 84	No