Pirfenidone for Subglottic Stenosis
What You Need to Know Before You Apply
What is the purpose of this trial?
Idiopathic subglottic stenosis (iSGS) is a rare condition where scar tissue forms just below the vocal cords and in the upper windpipe, making the airway narrow. People with iSGS often feel short of breath, hear noisy breathing, and notice changes in their voice. Many need repeated operations and steroid injections to open the airway, but the narrowing usually comes back, so these treatments are not a cure.
Recent research from a Canadian iSGS registry and biobank has shown that this disease is driven by overactive scarring pathways, similar to those seen in idiopathic pulmonary fibrosis (IPF), a serious lung disease. Pirfenidone is an oral medication already approved for IPF that works by slowing down the cells and signals that cause scarring. Because the same scarring pathways appear to be active in iSGS, pirfenidone may be able to slow or reduce the build-up of scar tissue in the airway.
In this study, adults with iSGS will be randomly assigned (like flipping a coin) to receive either pirfenidone or a placebo (a look-alike pill with no active drug) for 52 weeks, in addition to their usual intralesional steroid injections. The pirfenidone dose will be increased gradually over the first two weeks up to a regular dose taken three times a day with food, which is the same schedule used in patients with IPF. Participants and their doctors will not know which treatment they are getting until the end of the study, unless this needs to be revealed for safety reasons.
The main goal of this trial is to see how safe pirfenidone is for people with iSGS and how well they can tolerate taking it for one year. The study team will watch closely for side effects such as stomach upset, skin rash or sensitivity to sunlight, tiredness, and changes in liver blood tests. They will also look for early signs that pirfenidone may help, such as longer time until the next airway dilation, better breathing tests, and improvements in breathlessness and voice-related quality of life scores.
Participants will be followed for a total of up to two years, including one year on study medication and one year of follow-up. This study may not directly help every person who takes part, but the results will provide important information about whether pirfenidone is safe in iSGS and whether it could become the first medication to slow down this scarring airway disease.
Are You a Good Fit for This Trial?
Inclusion Criteria
Exclusion Criteria
What Are the Treatments Tested in This Trial?
How Is the Trial Designed?
2
Treatment groups
Experimental Treatment
Placebo Group
Participants in this arm will receive oral pirfenidone in addition to standardized intralesional steroid injections for idiopathic subglottic stenosis. Pirfenidone will be titrated from 801 mg/day in Week 1 to 1,602 mg/day in Week 2, then to a maintenance dose of 2,403 mg/day (801 mg three times daily) from Week 3 through Week 52, as tolerated. Study drug will be taken with food to reduce gastrointestinal side effects. All participants will continue to receive protocolized intralesional steroid injections as part of their usual airway management. Participants will be followed during treatment and for an additional post-treatment follow-up period to assess safety, tolerability, and preliminary efficacy.
Participants in this arm will receive an oral placebo in addition to standardized intralesional steroid injections for idiopathic subglottic stenosis. The placebo capsules will be identical in appearance and dosing schedule to pirfenidone, including titration over the first 2 weeks and maintenance dosing three times daily with food through Week 52. All participants will continue to receive protocolized intralesional steroid injections as part of their usual airway management. Participants will be followed during treatment and for an additional post-treatment follow-up period to assess safety, tolerability, and to compare outcomes with the pirfenidone arm.
Find a Clinic Near You
Who Is Running the Clinical Trial?
London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
Lead Sponsor
Unity Health Toronto
Collaborator
Unbiased Results
We believe in providing patients with all the options.
Your Data Stays Your Data
We only share your information with the clinical trials you're trying to access.
Verified Trials Only
All of our trials are run by licensed doctors, researchers, and healthcare companies.