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Recruiting Phase 2 Interventional

Oral Ifetroban in Patients With Idiopathic Pulmonary Fibrosis (IPF)

ClinicalTrials.gov ID: NCT05571059

Public ClinicalTrials.gov record NCT05571059. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 4:39 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-Blind, Placebo-Controlled Phase II Study to Determine the Safety and Efficacy of Oral Ifetroban in Patients With Idiopathic Pulmonary Fibrosis (IPF)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Ifetroban prevents and treats lung fibrosis due to multiple causes (bleomycin, genetic, radiation). The safety and efficacy of oral ifetroban will be assessed in patients with IPF.

Study identification

NCT ID
NCT05571059
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
Cumberland Pharmaceuticals
Industry
Enrollment
128 participants

Conditions and interventions

Eligibility (public fields only)

Age range
40 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 30, 2024
Primary completion
Dec 31, 2026
Completion
Dec 31, 2026
Last update posted
Mar 4, 2026

2024 – 2027

United States locations

U.S. sites
19
U.S. states
15
U.S. cities
19
Facility City State ZIP Site status
Biosolutions Clinical Research La Mesa California 91942 Recruiting
University of California San Francisco San Francisco California 94143 Recruiting
Mayo Clinic Jacksonville Jacksonville Florida 32224 Recruiting
Miami VA Health System Miami Florida 33125 Recruiting
Northwestern Medicine Chicago Illinois 60611 Recruiting
Indiana University Health Indianapolis Indiana 46202 Recruiting
University of Kansas Kansas City Kansas 66160 Recruiting
University of Louisville Louisville Kentucky 40202 Recruiting
Beaumont Hospital, Royal Oak Royal Oak Michigan 48073 Recruiting
Icahn School of Medicine at Mount Sinai New York New York 10029 Recruiting
University of Rochester Rochester New York 14642 Recruiting
UNC Chapel Hill Chapel Hill North Carolina 27514 Recruiting
Bend Memorial Hospital Bend Oregon 97701 Recruiting
Temple University Hospital Philadelphia Pennsylvania 19140 Recruiting
Avera Research Institute Sioux Falls South Dakota 57108 Recruiting
Pulmonary & Sleep Specialists Dickson Tennessee 37055 Recruiting
Baylor University Medical Center Dallas Texas 75246 Recruiting
Premier Pulmonary Critical Care and Sleep Medicine Denison Texas 75020 Recruiting
UW Health University Hospital Madison Wisconsin 53792 Recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05571059, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 4, 2026 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05571059 live on ClinicalTrials.gov.

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