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Pulmonary Hypertension Screening in Patients With Interstitial Lung Disease for Earlier Detection (PHINDER)

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United Therapeutics

Status

Enrolling

Conditions

Pulmonary Hypertension
Interstitial Lung Disease

Treatments

Procedure: Right heart catheterization (RHC)

Study type

Observational

Funder types

Industry

Identifiers

NCT05776225
GMS-PH-001

Details and patient eligibility

About

Study GMS-PH-001 is a multicenter, open-label, non-randomized study to prospectively evaluate screening strategies of pulmonary hypertension (PH) in patients with interstitial lung disease (ILD).

Full description

In this study, subjects will undergo a broad range of clinical assessments that are potentially associated with PH. Study data will be used to identify and weigh specific clinical parameters based on their prognostic significance for right heart catheterization (RHC)-confirmed PH. There is no study drug under investigation in this study. The study consists of 2 study visits: a Screening Visit and Study Visit 1.

Clinical assessments include pulmonary function tests (PFTs); high resolution computed tomography (HRCT); physical examination; 6-Minute Walk Test; blood draw for clinical laboratory parameters, plasma brain natriuretic peptide (BNP) concentration and plasma N-terminal pro-BNP (NT-proBNP) concentration; echocardiography; University of California San Diego Shortness of Breath Questionnaire (UCSD SOBQ); King's Brief Interstitial Lung Disease Questionnaire (K-BILD); 36-Item Short Form Survey (SF-36); Pulmonary Hypertension Functional Classification Self Report (PH-FC-SR); Investigator's Suspicion of PH Questionnaire; adverse event (AE) monitoring; and RHC.

As the primary objective of this study is to collect a broad range of clinical parameters in patients with ILD, it is expected that numerous exploratory and post-hoc analyses will be performed to identify and weigh specific parameters based on their prognostic significance for PH in this patient population with the goal of developing a screening algorithm for PH in patients with ILD.

Enrollment

300 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria

  1. Patient gives voluntary written informed consent to participate in the study and are capable of reading and understanding questionnaires or forms in English or Spanish.

  2. Patients with a diagnosis of ILD based on computed tomography imaging, including:

    1. Idiopathic interstitial pneumonia, including idiopathic pulmonary fibrosis
    2. Connective tissue disease-associated ILD with forced vital capacity (FVC) <70%
    3. Hypersensitivity pneumonitis
    4. Scleroderma-related ILD
    5. Autoimmune ILD
    6. Nonspecific interstitial pneumonia
    7. Occupational lung disease
    8. Combined pulmonary fibrosis and emphysema with mild emphysema on lung imaging as determined by the Investigator
  3. Patients must have at least 2 signs or symptoms suggestive of PH, as specified by the study protocol.

Exclusion Criteria

  1. Prior RHC with mPAP >20 mmHg.
  2. Currently on a Food and Drug Administration (FDA)-approved pulmonary arterial hypertension (PAH) medication for the treatment of PAH.
  3. Diagnosed with chronic obstructive pulmonary disease (CPFE with mild emphysema notwithstanding).
  4. Uncontrolled or untreated moderate to severe sleep apnea as determined by the patient's physician.
  5. Pulmonary embolism within the past 3 months.
  6. History of ischemic heart disease or left-sided myocardial dysfunction within 12 months of Screening, defined as left ventricular ejection fraction <40% or pulmonary capillary wedge pressure >15 mmHg.
  7. Any other clinical features that, in the opinion of the Investigator, might adversely affect interpretation of study data or study safety, or make the patient unsuitable for RHC or HRCT (e.g., pregnancy).

Trial design

300 participants in 1 patient group

Experimental study arm
Description:
All enrolled patients in this single arm study will receive a RHC.
Treatment:
Procedure: Right heart catheterization (RHC)

Trial contacts and locations

42

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Central trial contact

United Therapeutics Global Medical Information

Data sourced from clinicaltrials.gov

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