πŸ›οΈ Verified NIH Record β€’ Updated 2025-10-13

LYT-100 in Patients With Idiopathic Pulmonary Fibrosis (IPF) (NCT05321420)

A Randomized Double-blind, Four-Arm Active and Placebo-controlled Dose-Finding Trial to Evaluate the Efficacy, Tolerability, Safety and Dose Response of LYT-100 in Patients With Idiopathic Pulmonary Fibrosis (IPF)

πŸ”΅ Active, Not Recruiting Phase2 πŸ’Š Investigational Drug / Biologic Sponsor: PureTech

🩺 Plain-English Summary (8th-Grade Level)

This study a randomized, double-blind, four arm study to evaluate the safety and efficacy of LYT-100 compared to pirfenidone or placebo in adults with Idiopathic Pulmonary Fibrosis.

Who can join: Review the eligibility criteria below.

Location: University of Alabama Birmingham β€” Birmingham, Alabama

Age range: 40 Years

πŸ§ͺ Interventions in This Study

πŸ“‹ "Do I Qualify?" β€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria β†—

πŸ“ All Participating Trial Locations (103 Sites)

Showing the first 25 of 103 sites.

  • University of Alabama Birmingham β€” Birmingham, Alabama
  • Science 37 β€” Los Angeles, California
  • NewportNativeMD, Inc. β€” Newport Beach, California
  • Paradigm Clinical Research Centers, Inc. β€” Redding, California
  • Los Angeles Biomedical Research Institute at Harbor UCLA Medical Center β€” Torrance, California
  • University of Connecticut Health Center β€” Farmington, Connecticut
  • Accel Research Sites Network β€” DeLand, Florida
  • Harmony Medical Research Institute, Inc β€” Hialeah, Florida
  • Piedmont Healthcare, Inc. β€” Atlanta, Georgia
  • Clinical Research Investments β€” Decatur, Georgia
  • Indiana University School of Medicine β€” Indianapolis, Indiana
  • University of Kansas Medical Center β€” Kansas City, Kansas
  • Pulmonix β€” Greensboro, North Carolina
  • Southeastern Research Center β€” Winston-Salem, North Carolina
  • University of Cincinnati β€” Cincinnati, Ohio
  • Temple University β€” Philadelphia, Pennsylvania
  • Clinical Trials Center of Middle Tennessee β€” Franklin, Tennessee
  • Vanderbilt University Medical Center β€” Nashville, Tennessee
  • Baylor Scott & White Research Institute β€” Dallas, Texas
  • Renovatio Clinical - The Woodlands Research Center β€” The Woodlands, Texas
  • Pulmonary Associates of Richmond β€” Richmond, Virginia
  • TPMG Clinical Research β€” Williamsburg, Virginia
  • Instituto MΓ©dico de la FundaciΓ³n de Estudios Clinicos / FundaciΓ³n Estudios β€” Rosario, Santa Fe Province
  • Aprillus Asistencia e InvestigaciΓ³n β€” Buenos Aires,
  • CEMER Centro Medico de Enfermedades Respiratorias β€” Buenos Aires,

πŸ’° Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA Β§ 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

πŸ’‘ How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Review the official NIH record below to find the coordinating site.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
πŸ›οΈ View Official NIH Record β†—