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Completed Phase 2 Interventional

Safety, Tolerability, and Efficacy Study of Idiopathic Pulmonary Fibrosis

ClinicalTrials.gov ID: NCT01262001

Public ClinicalTrials.gov record NCT01262001. 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 Oct 30, 2026, 6:20 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 Phase 2, Open-Label, Dose-Escalation Study to Evaluate the Safety, Tolerability, and Efficacy of FG-3019 in Subjects With Idiopathic Pulmonary Fibrosis

Brief summary

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

To evaluate the safety and tolerability of FG-3019 in subjects with Idiopathic Pulmonary Fibrosis (IPF) and the efficacy of FG-3019 for attenuating fibrosis in these subjects.

Study identification

NCT ID
NCT01262001
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Kyntra Bio
Industry
Enrollment
90 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
35 Years to 80 Years
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
Mar 2011 (Type not available)
Primary completion
Jun 26, 2014 (Actual)
Completion
Jun 21, 2017 (Actual)
Last update posted
Oct 9, 2019

2011 – 2017

United States locations

U.S. sites
18
U.S. states
17
U.S. cities
18
Facility City State ZIP Site status
University of Alabama at Birmingham Hospital Birmingham Alabama 35294 —
Arizona Pulmonary Specialists, LTD Scottsdale Arizona 85258 —
Yale University New Haven Connecticut 06520 —
Central Florida Pulmonary Group, PA Orlando Florida 32803 —
Tampa General Hospital Tampa Florida 33606 —
Emory University Atlanta Georgia 30322 —
Via Christi Hospitals Wichita, Inc. Wichita Kansas 67208 —
University of Louisville Louisville Kentucky 40202 —
St. Luke's Hospital Chesterfield Missouri 63017 —
Rutgers-Robert Wood Johnson Medical School New Brunswick New Jersey 08901 —
Mount Sinai New York New York 10029 —
The Ohio State University Columbus Ohio 43221 —
Vanderbilt University Nashville Tennessee 37232 —
University of Texas Southwestern Medical Center Dallas Texas 75390 —
University of Utah - Lung Health Research Salt Lake City Utah 84108 —
Vermont Lung Center Colchester Vermont 05446 —
Inova Fairfax Hospital Falls Church Virginia 22042 —
University of Wisconsin School of Medicine & Public Health Madison Wisconsin 53705 —

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 NCT01262001, 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 Oct 9, 2019 · Synced Oct 30, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01262001 live on ClinicalTrials.gov.

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