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Clinical trialNCT04300920CompletedPhase 3Interventional

Prospective Treatment Efficacy in IPF Using Genotype for Nac Selection (PRECISIONS) Trial

SponsorFernando J MartinezEnrollment202Idiopathic Pulmonary Fibrosis
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

The purpose of this study is to compare the effect of n-acetylcysteine (NAC) plus standard care with matched placebo plus standard of care in patients diagnosed with idiopathic pulmonary fibrosis (IPF) who have the TOLLIP rs3750920 TT genotype. The study will compare the time to a composite endpoint of relative decline in lung function \[10% relative decline in forced vital capacity (FVC), first respiratory hospitalization, lung transplantation, or all-cause mortality\] The secondary objectives will be to examine the effect of NAC on the components of the primary composite endpoint, the rates of clinical events, change in physiology, change in health status, and change in respiratory symptoms.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

25 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • University of Arizona

    Tucson, Arizona, United States

  • University of Southern California

    Los Angeles, California, United States

  • Stanford University

    Stanford, California, United States

  • University of Colorado

    Aurora, Colorado, United States

  • Piedmont Healthcare

    Austell, Georgia, United States

  • University of Chicago

    Chicago, Illinois, United States

  • Loyola University

    Maywood, Illinois, United States

  • Indiana University

    Indianapolis, Indiana, United States

  • University of Kansas Medical Center

    Kansas City, Kansas, United States

  • Tulane University

    New Orleans, Louisiana, United States

  • Massachusetts General Hospital

    Boston, Massachusetts, United States

  • University of Michigan

    Ann Arbor, Michigan, United States

  • University of Minnesota

    Minneapolis, Minnesota, United States

  • Mayo Clinic

    Rochester, Minnesota, United States

  • Weill Cornell Medicine

    New York, New York, United States

  • University of Rochester

    Rochester, New York, United States

  • Ohio State University

    Columbus, Ohio, United States

  • Temple University

    Philadelphia, Pennsylvania, United States

  • Medical University of South Carolina

    Charleston, South Carolina, United States

  • Lisa Lancaster

    Nashville, Tennessee, United States

  • University of Texas Southwestern

    Dallas, Texas, United States

  • University of Texas Health San Antonio

    San Antonio, Texas, United States

  • University of Utah Health

    Salt Lake City, Utah, United States

  • University of Virginia

    Charlottesville, Virginia, United States

  • University of Washington

    Seattle, Washington, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov ↗

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
17 Dec 2020
Primary completion
2 Mar 2026
Completion
2 Mar 2026
Last update posted
20 Mar 2026
Registered enrollment
202
Registry id
NCT04300920

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.