20 Participants Needed

Sparsentan for Proteinuria After Kidney Transplant

(SPARX Trial)

Recruiting at 4 trial locations
TC
Overseen ByTravere Call Center
Age: 18+
Sex: Any
Trial Phase: Phase 4
Sponsor: Travere Therapeutics, Inc.
Must be taking: ACEI, ARB, SGLT2 inhibitors
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests the safety and effectiveness of sparsentan, a new medication, for individuals with proteinuria (excess protein in urine) following a kidney transplant. The goal is to determine if sparsentan can reduce protein levels and improve kidney function. This study targets those who had a kidney transplant over a year ago and have conditions like IgAN or FSGS, which are patterns of kidney disease. Participants should have stable blood pressure and no recent major infections or other serious medical conditions. As a Phase 4 trial, sparsentan has already received FDA approval and proven effective, and this research aims to understand how it benefits more patients.

Do I have to stop taking my current medications for the trial?

The trial does not specify if you must stop taking your current medications, but it requires that any immunosuppressive therapy (IST) regimen be stable for more than 6 weeks before starting the trial. If you're on an ACEI, ARB, or SGLT2 inhibitor, your dose must also be stable for at least 6 weeks before screening.

What is the safety track record for sparsentan?

Research has shown that sparsentan is generally well-tolerated. In a study comparing sparsentan to irbesartan, sparsentan significantly reduced protein in the urine, a positive sign for kidney health. The study also found that sparsentan maintained kidney function better than irbesartan.

While all medications carry some risks, sparsentan's safety appears promising based on these results. This trial is in Phase 4, indicating the drug is already approved for other uses, which adds confidence about its safety. However, discussing any concerns with the study team or a healthcare provider before joining a clinical trial is important.12345

Why are researchers enthusiastic about this study treatment?

Unlike the standard treatments for proteinuria after a kidney transplant, which often involve immunosuppressive drugs, sparsentan is unique because it is a non-immunosuppressive option. It works by dual antagonism of receptors ETAR and AT1R, offering a potent anti-proteinuric effect. Researchers are excited about sparsentan because of its potential to reduce proteinuria effectively without the side effects associated with immunosuppressants.

What evidence suggests that sparsentan might be an effective treatment for proteinuria after kidney transplant?

Research has shown that sparsentan can significantly reduce proteinuria, a common issue after a kidney transplant characterized by excess protein in the urine. In earlier studies, sparsentan lowered proteinuria by 62% after 14 weeks and maintained this reduction over time. It also resulted in more individuals experiencing partial or complete remission of proteinuria compared to other treatments. Sparsentan works by blocking two pathways that cause kidney damage, thereby reducing protein levels in the urine. These findings suggest sparsentan could be effective for individuals dealing with proteinuria after a kidney transplant.26789

Who Is on the Research Team?

RK

Radko Komers, MD, PhD

Principal Investigator

Travere Therapeutics

Are You a Good Fit for This Trial?

This trial is for individuals who have had a kidney transplant and are now experiencing proteinuria due to IgA Nephropathy or Focal Segmental Glomerulosclerosis. Participants should be stable post-transplant and not currently receiving certain other treatments that could interfere with the study.

Inclusion Criteria

Willing and capable of giving signed informed consent which includes compliance with the requirements and restrictions listed in the ICF and in the protocol
Participants who can become pregnant, must agree to the use of 1 highly reliable method of contraception from 7 days prior to the first dose of study intervention until 30 days after the last dose of study intervention
Systolic BP ≤160 mmHg and ≥100 mmHg, and diastolic BP ≤100 mmHg and ≥60 mmHg at screening
See 5 more

Exclusion Criteria

History of alcohol or illicit drug use disorder
History of serious side effects or allergic response to any angiotensin II antagonist or ERA
Participant has participated in a study of another investigational product <28 days prior to screening or plans to participate in such a study during the course of this study
See 14 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive sparsentan treatment for 36 weeks with dose adjustments based on kidney transplant type

36 weeks
Visits at Day 5 and Weeks 2, 4, 6, 12, 24, and 36

Follow-up

Participants are monitored for safety and effectiveness after treatment during a 4-week off-sparsentan period

4 weeks
Telephone visit at Week 40

What Are the Treatments Tested in This Trial?

Interventions

  • Sparsentan
Trial Overview The trial is testing the safety and effectiveness of sparsentan tablets in reducing proteinuria over a period of 36 weeks. Patients will take sparsentan once daily, and their response to treatment will be closely monitored.
How Is the Trial Designed?
1Treatment groups
Experimental Treatment
Group I: Drug: SparsentanExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Travere Therapeutics, Inc.

Lead Sponsor

Trials
23
Recruited
103,000+

Citations

Study Details | NCT07219121 | Sparsentan in ...To evaluate the safety and efficacy of sparsentan tablets for the treatment of patients with proteinuria after kidney transplantation with once- ...
Sparsentan for treating primary IgA nephropathy - NCBI - NIHThe primary outcome was the percentage change in UPCR from baseline to week 36. Sparsentan statistically significantly reduced proteinuria ...
Sparsentan for Halting Renal Disease Progression in ...Purpose: Here we present a case demonstrating Sparsentan's role in preventing renal disease progression in a transplant patient with recurrent IgA nephropathy.
First real-world evidence of sparsentan efficacy in patients ...Sparsentan shows a significant impact on proteinuria, leading to a relative reduction of 62% in UPCR after 14 weeks and beyond, even in patients already ...
Sparsentan Decreased Proteinuria, but Failed to Slow ...There was also a higher incidence of partial remission (37.5% vs. 22.6%) and complete remission (18.5% vs. 7.5%) in proteinuria with sparsentan ...
Real-world assessment of sparsentan's drug safety frameworkCompared to the irbesartan group, sparsentan demonstrated remarkable renal function preservation and a significant reduction in proteinuria.
Filspari, INN-sparsentan - European Medicines AgencyThe uncertainties in the 2-year eGFR efficacy data are considered small and of low risk given the predictive nature of proteinuria reduction on ...
PROTECT STUDY - FILSPARI® (sparsentan)Review the clinical study design to see how the efficacy and safety of FILSPARI® (sparsentan) was evaluated. See Safety Info.
Sparsentan versus Irbesartan in Focal Segmental ...At 36 weeks, the percentage of patients with partial remission of proteinuria was 42.0% in the sparsentan group and 26.0% in the irbesartan ...
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