Sparsentan for Proteinuria in Cancer Patients

This study is looking at whether sparsentan can help reduce high levels of protein in the urine (proteinuria) for people with cancer who are also taking certain other cancer medications called VEGF signaling pathway inhibitors (VSPIs). You might be able to join if you are an adult (18 or older) with cancer, are currently taking VSPIs, and have new, high-grade proteinuria. The study will measure the change in your urine protein levels after 8 weeks to see if sparsentan is effective. The current recruitment status is unclear.

Study design
This is a single-center, open-label pilot study. It plans to include 20 participants.
What's involved
Participants will take sparsentan 200 mg daily for 2 weeks, then increase to 400 mg daily. Your urine protein to creatinine ratio will be assessed from screening to week 8.
Compensation
Not stated in the trial record.
Follow-up
Your urine protein levels will be measured at 8 weeks after starting the study.

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NCT07224776

Sparsentan for the Treatment of VEGF Signaling Pathway Inhibitor-Associated Proteinuria

Recruiting
PHASE1Ages 18+InterventionalTreatment
Brigham and Women's Hospital
~20 participants
Updated 2026-07-30 on ClinicalTrials.gov
What's tested:sparsentanNo sparsentan

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Change in urine to protein creatinine ratio (UPCR)
Measured over 8 weeks
Proteinuric Renal Disease
Proteinuric Kidney Disease
Proteinuria
Proteinuria in Nephrotic Range
1 sites across 1 states
Massachusetts1

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  • Change in urine to protein creatinine ratio (UPCR)8 weeks

    The geometric mean percent change in UPCR from screening day to Week 8