Study of INS018_055 for Idiopathic Pulmonary Fibrosis
This study is testing a new medication called INS018_055 for people with Idiopathic Pulmonary Fibrosis (IPF). IPF is a serious lung disease that makes it hard to breathe. Current treatments can have side effects, so researchers are looking for new options. INS018_055 works by targeting a specific protein called RAF. In this study, some participants will receive INS018_055 as a tablet, and others will receive a placebo (an inactive tablet). The main goal is to see how safe INS018_055 is over 12 weeks by tracking any side effects. You may be able to join if you are at least 40 years old and have a diagnosis of IPF. The study is currently unclear on its recruitment status.
- Study design
- This interventional study plans to enroll 40 participants. It compares INS018_055 tablets to placebo tablets.
- What's involved
- You would take either INS018_055 or a placebo tablet. Your safety will be monitored from Day 1 up to Week 12.
- Compensation
- Not stated in the trial record.
- Follow-up
- Your safety will be monitored up to Week 12 (End of Treatment).
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Study Evaluating INS018_055 Administered Orally to Subjects With Idiopathic Pulmonary Fibrosis
At a glance
Conditions
NCT05975983
Where you'd take part
This study runs at 12 sites. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
Bogan Sleep Consultants, LLC
Columbia, South Carolinano site contact published
Recruiting
Central Florida Pulmonary Group, P.A. (CFPG) - Downtown Orlando
Orlando, Floridano site contact published
Recruiting
Florida Lung Asthma and Sleep Specialist
Celebration, Floridano site contact published
Recruiting
HonorHealth Research Institute
Scottsdale, Arizonano site contact published
Recruiting
Keck School of Medicine of USC
Los Angeles, Californiano site contact published
Recruiting
Metroplex Pulmonary and Sleep Center
McKinney, Texasno site contact published
Recruiting
Research Centers of America
McKinney, Texasno site contact published
Recruiting
Southeastern Research Center
Winston-Salem, North Carolinano site contact published
Recruiting
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Who to contact
Opens a ready-to-send draft in your own email app — review before sending.
What this trial measures
- Percentage of subjects who have at least 1 treatment-emergent adverse event (TEAE)Day 1 (Visit 2) up to Week 12 (End of Treatment (EOT))