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A Study to Access Activity and Safety With SAR445399 Compared With Placebo in Participants Aged 18 to 80 Years of Age With Non-Cystic Fibrosis Bronchiectasis

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NCT07547436 · readout in 436 d

Sponsored by Sanofi (industry) · SNY — their whole pipeline →.

Phase
Phase 2
Status
Suspended
Study type
Interventional
Design
Randomized · Quadruple · Treatment
Enrollment
70estimated
Sites
4
Country
United States

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

Why the sponsor stopped it

The pause is for strategic business reasons to facilitate internal portfolio review. The pause is not due to any concerns with patient safety, with program benefit/risk, or with trial integrity.

As filed on the registry record, in the sponsor's own words.

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2026-06-08actualWhen the study began enrolling
Primary completion2027-10-29estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2029-05-11estimatedThe whole study's end, after follow-up
First posted2026-04-23actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-07-29actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Non-cystic Fibrosis Bronchiectasis

Interventions

  • Biological: SAR445399
  • Biological: Placebo

Primary outcome

what the primary-completion date above is the date OF
Change from baseline to Week 24 in mucus plug score (MPS) derived from chest high-resolution computerized tomography (HRCT)
measured from baseline up to Week 24

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