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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

Recruiting · Phase 2 · NCT06500702

Conditions: Focal Segmental Glomerulosclerosis, Glomerulonephritis Minimal Lesion

At a glance

Research payments reported, 2025
$538,301
U.S. investigators named
15
Sites paid
13
Planned or actual enrollment
84

About the trial

Sponsor
Sanofi
Tested
frexalimab (drug), brivekimig (drug), rilzabrutinib (drug), placebo (drug)
Dates
Started 2024-12-19; completion 2028-02-16
Results posted
Not yet

This is a parallel, Phase 2a, double-blind, 6-arm study for the treatment of primary focal segmental glomerulosclerosis (FSGS) or minimal change disease (MCD). The purpose of this study is to measure the change in proteinuria and its impact on the rates of remission of nephrotic syndrome with frexalimab, brivekimig or rilzabrutinib compared with placebo in participants with primary FSGS or MCD aged 16 to 75 years. Study details for each participant include: The study duration will be up to 52 weeks. The treatment duration will be 24 weeks. There will be up to 16 visits.

From ClinicalTrials.gov, last updated 2026-10-19. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Genzyme Corporation reported $538,301 in research payments for this study in 2025 (55 payments).

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.