πŸ›οΈ Verified NIH Record β€’ Updated 2025-11-10

Study Evaluating INS018_055 Administered Orally to Subjects With Idiopathic Pulmonary Fibrosis (NCT05975983)

A Phase IIa, Randomized, Double-Blind, Placebo-Controlled Study Evaluating the Safety, Tolerability, Pharmacokinetics, and Efficacy of INS018_055 Administered Orally to Subjects With Idiopathic Pulmonary Fibrosis (IPF)

🟒 Recruiting Phase2 πŸ’Š Investigational Drug / Biologic Sponsor: InSilico Medicine Hong Kong Limited

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

The purpose of this revised Phase IIa study is to demonstrate safety of INS018\_055 over 12 weeks in adults with Idiopathic Pulmonary Fibrosis (IPF).

Who can join: Review the eligibility criteria below.

Location: University of Alabama at 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 (12 Sites)

  • University of Alabama at Birmingham β€” Birmingham, Alabama
  • HonorHealth Research Institute β€” Scottsdale, Arizona
  • Keck School of Medicine of USC β€” Los Angeles, California
  • Florida Lung Asthma and Sleep Specialist β€” Celebration, Florida
  • Central Florida Pulmonary Group, P.A. (CFPG) - Downtown Orlando β€” Orlando, Florida
  • Southeastern Research Center β€” Winston-Salem, North Carolina
  • University of Oklahoma Health Sciences Center (OUHSC) β€” Oklahoma City, Oklahoma
  • Temple University Hospital-Temple Lung Center β€” Philadelphia, Pennsylvania
  • Bogan Sleep Consultants, LLC β€” Columbia, South Carolina
  • University of Texas Southwestern Medical Center β€” Dallas, Texas
  • Metroplex Pulmonary and Sleep Center β€” McKinney, Texas
  • Research Centers of America β€” McKinney, Texas

πŸ“ž Contact the Study Coordinator

Phone: +86 18817554306

Email: Insilico-Clinicaltrial@insilico.ai

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

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. Contact the study coordinator using the phone/email above.
  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†—