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Early Feasibility Study Evaluating the 3P-100 Device in Subjects With PH-ILD — EFS  

Hypertension, Pulmonary Clinical Trial

Official title:
A Within-subject Device-setting Escalation Early Feasibility Study Evaluating the Safety, Tolerability, and Functionality of 3P-100 in Subjects With PH-ILD

Clinical Trial Summary

A trial to evaluate the safety, tolerability, and functionality of 3P-100, in subjects with Pulmonary Hypertension (PH) accompanying Interstitial Lung Disease (ILD), PH-ILD

Clinical Trial Description

This is a multi-center early feasibility study evaluating the safety and tolerability of the 3P-100 device which creates and delivers iNO (2 mg/hr and 6 mg/hr) for the treatment of subjects with PH-ILD. All subjects will use the 3P-100 device and receive iNO (2 mg/hr and 6 mg/hr) via the 3P-100 device, aiming for ~4-4.5 hours of treatment across both device settings. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05867914
Study type Interventional
Source Third Pole Therapeutics, Inc.
Contact
Status Active, not recruiting
Phase N/A
Start date December 4, 2023
Completion date March 29, 2024
View Details
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