Purpose of this Study
We are doing this study to find out if an investigational drug called belumosudil (the study drug) is an option for the treatment of chronic lung allograft dysfunction (CLAD). The study drug is taken by mouth.
Who Can Participate?
Eligibility
Adults who:
- Received a bilateral lung transplant at least 1 year ago
- Are diagnosed with progressive CLAD that is stage 1 or 2
- Have been on azithromycin for at least 8 weeks at the time of joining the study
- Have not had any previous treatment for CLAD
Age Range
18-110
Sex/Genders
Male (cisgender)
Female (cisgender)
Non-binary or gender fluid
Transgender male
Transgender female
Looking for Healthy Participants
No
What is Involved?
Description
The study is divided into five periods: screening period, randomized period, open-label extension (OLE) period, long-term OLE period, and safety follow-up period. If you choose to join the study, you may participate in the following:
Screening Period
This period includes 1 study visit to determine if you are a good candidate for the study.
The screening visit includes reviewing and signing a consent form, completing breathing tests, having a physical exam, getting an electrocardiogram, and having blood draws.
Randomized Period
During this period of the study, you will get a random assignment to either:
- Take the study drug once or twice a day for 26 weeks; OR
- Take a placebo (inactive substance with no drug in it) once or twice a day for 26 weeks
Locations
Duke University Hospital
Visit Timing
Weekdays
Compensation
Yes
Spanish Materials Available
No
Study Details
Full Title
A randomized, double-blind, placebo-controlled, parallel group, Phase 3 study, followed by open-label extensions, to evaluate the efficacy of oral belumosudil in adult participants with chronic lung allograft dysfunction (CLAD) following bilateral lung transplantation
Principal Investigator
Jamie
Todd
Protocol Number
PRO00113681
NCT ID
NA
Phase
III
Enrollment Status
Open to Enrollment