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A Study to Evaluate the Efficacy and Safety of Frexalimab, Brivekimig, or Rilzabrutinib in Participants Aged 16 to 75 Years With Primary Focal Segmental Glomerulosclerosis or Minimal Change Disease

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NCT06500702 · readout in 126 d

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

Phase
Phase 2
Status
Recruiting
Study type
Interventional
Design
Randomized · Quadruple · Treatment
Enrollment
84estimated
Sites
71
Countries
Argentina, Australia, Brazil +19

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
Start2024-12-19actualWhen the study began enrolling
Primary completion2026-12-23estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2028-02-16estimatedThe whole study's end, after follow-up
First posted2024-07-15actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-07-20actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Focal Segmental Glomerulosclerosis
  • Glomerulonephritis Minimal Lesion

Interventions

  • Drug: frexalimab
  • Drug: brivekimig
  • Drug: rilzabrutinib
  • Drug: placebo

Primary outcome

what the primary-completion date above is the date OF
Percent reduction in urine protein to creatinine ratio (UPCR)
measured From baseline to Week 12

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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