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A Study to Test How Effective Belumosudil Tablets Are for Treating Adult Participants With Chronic Lung Allograft Dysfunction

← catalyst calendar

NCT06082037 · readout in 894 d

Sponsored by Sanofi (industry) · SNY — their whole pipeline →. With Meiji Seika Pharma Co., Ltd..

Phase
Phase 3
Status
Recruiting
Study type
Interventional
Design
Randomized · Quadruple · Treatment
Enrollment
180estimated
Sites
79
Countries
Australia, Austria, Belgium +16

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2023-10-10actualWhen the study began enrolling
Primary completion2029-01-29estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2030-10-01estimatedThe whole study's end, after follow-up
First posted2023-10-13actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-06-29actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Lung Transplant Rejection

Interventions

  • Drug: Belumosudil — also filed as REZUROCK
  • Drug: Azithromycin
  • Drug: Placebo

Primary outcome

what the primary-completion date above is the date OF
Percent change from baseline to Week 26 in forced expiratory volume in 1 second (FEV1)
measured Baseline to Week 26

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