Rare Kidney Disease Show

In this episode the Rare Kidney Disease Show, our host Chris Gisler is joined by Dr. Chee Kay Cheung from the University of Leicester to discuss the changing of proteinuria targets in the treatment of IgAN and to explore the question of whether achieving very low levels of proteinuria tell us something meaningful about the future trajectory of kidney function.  They discuss why targets have changed, what exactly has changed, and why the definition of a good treatment response has become more ambitious. Through discussion of RaDaR: a real-world observational data from the UK National Registry of Rare Kidney Diseases with analysis including 2,439 participants with biopsy-proven IgAN, including 2,299 adults and 140 children and the PROTECT Study: a randomized, double-blind, active-controlled phase 3 study evaluating sparsentan in adults with biopsy-proven primary IgAN and persistent proteinuria despite a maximally tolerated dose of RAS inhibition that was at least one-half of the maximum labeled dose they dive deeper into proteinuria and prognosis and the potential for complete remission and slowing of eGFR decline.Speakers:Dr. Chris Gisler is a medical director at Travere Therapeutics and an adult NephrologistDr. Chee Kay Cheung, MBChB, MRCP, PhD, FHEA, is a Consultant Nephrologist and Honorary Associate Professor at the University Hospitals of Leicester NHS Trust, UK, with expertise in glomerular diseases, IgA nephropathy, vasculitis, and lupus nephritisKey Takeaways:The lower the proteinuria the better, there is no “safe” threshold. IgA nephropathy risk does not disappear below 1 g/day. Even modest residual proteinuria is associated with meaningful lifetime kidney-failure risk, supporting more ambitious targets of <0.5 g/day and ideally <0.3 g/day.Complete proteinuria remission is associated with substantially better kidney outcomes. In the post hoc PROTECT analysis, patients achieving proteinuria <0.3 g/day had slower annual eGFR decline (−0.7 vs. −4.2 mL/min/year) and fewer composite kidney events (1% vs. 14%) than those who did not achieve remission. Proteinuria and eGFR should be treated as complementary measures.Preserving eGFR and preventing kidney failure remain the ultimate goals, while proteinuria provides an earlier, actionable indicator of disease activity and residual risk. The clinical implication is to diagnose earlier, treat more aggressively, and escalate therapy when proteinuria remains above target.Key Quotes:"Previous targets really reflected the available evidence at the time. But much of this was derived from relatively small studies, maybe a few hundred patients, from small numbers of centers. And patients were followed for a relatively brief period of time, maybe 5 to 10 years. More recent registry data has included far larger numbers of patients, followed for a much longer period of time. And now we're really thinking about the lifetime risk that people have of developing kidney function decline or kidney failure.""More recent observational data, and this is data from the RADAR study, but also US data from the Kaiser Permanente database, from China, from Sweden, emphasizes, really, that the lower we can drive proteinuria, the better the outcomes.""With both sparsartan and irbesartan, when you exclude the first 6 weeks and look at the GFR slope for the remainder of the study, the eGFR decline was -0.7 mL/min/year in the complete remission group, versus -4.2 mL/min/year in the non-remission group. So, that between-group difference in the chronic eGFR slope was very statistically significant. And actually, that observed rate of -0.7 mL/min/year achieved that KDIGO target of achieving a slope decline of less than 1 mL/min/year for the rest of the patient's life."Disclaimer:Guest speakers of the Rare Kidney Disease Show may be paid consultants of Travere Therapeutics. This podcast episode was recorded on September 29, 2026. Please always consult updated sources for the latest information, as information discussed may have changed since the recording date.

Welcome to Travere Therapeutics’ Rare Kidney Disease Show podcast, where rare kidney disease gets a spotlight. Host Dr. Chris Gisler, Senior Medical Director at Travere Therapeutics, is joined by Dr. Daniel Gale and Dr. Gaia Coppock for a practical and evidence-driven conversation on FSGS, proteinuria, and what registry and clinical data mean for clinical decision-making.In this episode, Dr. Gaia Coppock reflects on how the heterogeneous nature of focal segmental glomerulosclerosis (FSGS) has historically been challenging for clinicians and highlights we are working towards a new era of research, diagnosis, and therapeutics. From there, the discussion focuses on FSGS as a podocytopathy, outlining different triggering events that converge on podocyte injury and shared downstream pathways. Dr. Daniel Gale goes on to discuss how RaDaR, PARASOL, and other real-world datasets have helped clarify the relationship between proteinuria remission and long-term kidney outcomes.The conversation also explores the Phase 3 DUPLEX study. Dr. Coppock reviews the study design and key findings, including reductions in proteinuria, data on complete remission, safety profiles, and the challenges of interpreting estimated glomerular filtration rate (eGFR) slope in a complex and heterogeneous condition like FSGS. Together, experts reflect on where FSGS care is heading, underscoring the importance of targeting lower proteinuria thresholds, improving diagnostic precision, and adopting multi-targeted approaches.Speakers:Dr. Chris Gisler is a medical director at Travere Therapeutics and an adult NephrologistDr. Daniel Gale, MBBS, PhD (Professor of Nephrology, University College London. Director, RaDaR/Rare Renal Registry)Dr. Gaia Coppock, MD (Assistant Professor of Clinical Medicine, Renal-Electrolyte and Hypertension. University of Pennsylvania/Penn Medicine)Key Takeaways:FSGS is a heterogeneous pattern of injury, not a single condition. FSGS can arise from multiple causes, which has historically made diagnosis, treatment, and clinical trial design difficultProteinuria is one of the most important clinical signals in FSGS. RaDaR and PARASOL have helped validate what clinicians have long suspected: lower proteinuria targets matter, and proteinuria can serve as a meaningful predictor of disease activity and response DUPLEX <helped clarify how proteinuria reduction in a clinical trial can be interpreted in FSGS>, especially in a condition where eGFR slope can be difficult to assess because of heterogeneity, hyperfiltration, and variability in kidney functionThe future of FSGS care depends on pushing to achieve the lowest proteinuria targets possible while becoming more precise in diagnosis and treatmentKey Quotes:“Proteinuria really represents a very strong biomarker of disease activity, rather than simply a readout of how much damage has occurred in the kidney.” (6:08)“I think that clinicians should push harder with FSGS. You know, don't stop until you've exhausted all options and really push to get to the lowest proteinuria target possible.” (25:59)"I think the use of FSGS as a disease label is now really established to be doing more harm than good for many patients. It's the start of the diagnostic journey, not the end of it.” (26:27)Disclaimer:Guest speakers of the Rare Kidney Disease Show may be paid consultants of Travere Therapeutics. This podcast episode was recorded on June 9, 2026. Please always consult updated sources for the latest information, as information discussed may have changed since the recording date.

Welcome to Travere Therapeutics’ Rare Kidney Disease podcast, where rare kidney disease gets a spotlight. Host Chris Gisler brings together two leading voices in nephrology, Dr. Donald Kohan and Dr. Yelena Drexler, for an energetic conversation about why proteinuria matters so much in FSGS and IgA nephropathy.What starts as a discussion of proteinuria as a lab value soon deepens: what is it, why does it mean more than just numbers, and how does it actually drive kidney injury? Dr. Donald Kohan breaks down the biology of endothelin, showing its role at every stage of glomerulonephritis. Then, Dr. Yelena Drexler links research to real patient care and shares the practical impact of proteinuria on outcomes.Whether you’re a clinician, researcher, or patient advocate, this episode delivers clear takeaways—from the latest studies shaping proteinuria targets to the call for multi-pathway, biology-informed treatment strategies.Speakers:Dr. Chris Gisler is a medical director at Travere Therapeutics and an adult NephrologistDr. Donald Kohan is a Professor of Medicine, Division of Nephrology & Hypertension at the University of UtahDr. Yelena Drexler is an Associate Professor of Clinical Medicine, Division of Nephrology & Hypertension at the University of Miami Key Takeaways:Proteinuria is both a marker and a driver of FSGS and IgAN, actively fueling inflammation, fibrosis, and a “vicious cycle” of ongoing injury, thereby making early and sustained reduction a critical treatment goalPodocyte injury is the central pathway in glomerular diseases like FSGS, with diverse causes converging on podocyte loss, leading to proteinuria and irreversible kidney damageEndothelin is a key mechanistic driver across the kidney, directly damaging podocytes and other cell types while working synergistically with the renin-angiotensin system to accelerate disease progressionKey Quotes:“Fundamentally, FSGS is a podocytopathy. And proteinuria is so important because it's a signature of podocyte loss, it's a signature of podocyte injury” 07:48“Persistent proteinuria to me is really a sign of ongoing podocyte injury and ongoing podocyte loss and the formation of sclerosis, focal and segmental glomerulosclerosis, that ultimately is irreversible. And we want to intervene to prevent that” 10:47“We’re not just thinking about proteinuria as a marker of disease. Proteinuria itself can actually worsen kidney injury… And you end up with a vicious cycle - the more injury you get, the more proteinuria you get and then the cycle continues” 11:23"As we're thinking about targeting the endothelin system, we have to think this system is activated throughout the entire course of the disease. And if we're going to target it, we've got to target it throughout the entire course of the disease” 17:50Disclaimer: Guest speakers of the Rare Kidney Disease Show may be paid consultants of Travere Therapeutics. This podcast episode was recorded on March 6, 2026. Please always consult updated sources for the latest information, as information discussed may have changed since the recording date.

In this episode, Drs. Jonathan Barratt and Shikha Wadhwani discuss findings from the SPARTAN study, a Phase 2 open-label, single-arm trial evaluating sparsentan in 12 treatment-naïve patients with IgA nephropathy. The conversation explores the trial’s design, including assessments of proteinuria reduction and urinary biomarkers to better understand sparsentan’s mechanism of action. Results from SPARTAN demonstrate a 69% mean reduction in proteinuria at 24 weeks, alongside biomarker trends consistent with decreased glomerular inflammation.  Dr. Barratt notes that no new safety signals emerged, with hypotension observed at a rate consistent with prior studies and no adverse hepatic events reported. Together, the experts reflect on how these data support the biological plausibility of sparsentan’s anti-inflammatory properties and may inform the development of biomarker-guided strategies in IgA nephropathy, including ongoing evaluation of sparsentan in the PROTECT trial.  Key Takeaways:SPARTAN demonstrated a robust mean reduction in proteinuria (~69%) in treatment-naïve patients with IgA nephropathy after 24 weeks of sparsentan therapy.Biomarker analysis revealed reductions in markers of macrophage activation, complement activity, and inflammatory cytokines, supporting the hypothesis of a potential anti-inflammatory effect.No new safety signals were observed; hypotension rates were consistent with earlier trials, and no clinically significant changes in hepatic function were reported.These findings contribute to our mechanistic understanding of sparsentan and provide a framework for future investigation of biomarkers from samples from larger studies such as PROTECT. Speakers:  Dr. Jonathan Barratt, PhD, FRCP. Professor of Renal Medicine at the University of Leicester, where he leads the IgA Nephropathy Research Programme. He is internationally recognized for his leadership in translational and clinical research in glomerular diseases, particularly IgA nephropathy. Dr. Barratt directs the UK’s Rare Disease Group for the UK National Registry of Rare Kidney Diseases (RaDaR).Dr. Shikha Wadhwani, MD, MS, FASN. Associate Professor of Medicine in the Division of Nephrology and Vice Chair of Clinical Research in the Department of Medicine at University of Texas Medical Branch. She is also the inaugural Associate Research Officer for clinical research, overseeing clinical trials across all 5 schools at UTMB. She is the founding member of the International Society of Glomerular Disease (ISGD) and is steering a global effort aimed at supporting the growth and success of physician-trialists. In her spare time, Dr. Wadhwani co-hosts a podcast called Kidney Compass: Navigating Clinical Trials.  Disclaimer: Guest speakers of the Rare Kidney Disease Show may be paid consultants of Travere Therapeutics. This podcast episode was recorded on July 25, 2025. Please always consult updated sources for the latest information, as information discussed may have changed since the recording date.

In this episode, Drs. Tobias Huber and Chris Gisler take a deep dive into the critical role of podocytes in kidney health and their involvement in the development and progression of FSGS. They explore how podocyte injury leads to the breakdown of the glomerular filtration barrier and the emergence of proteinuria. They highlight the intertwined roles of endothelin 1 and angiotensin II in worsening podocyte dysfunction and driving disease progression. They discuss current and emerging data, treatment options, and biomarkers, including findings from Dr. Huber’s latest research. Lastly, they emphasize the value of proteinuria as both a marker and mediator of podocyte damage, reinforcing its role as a key therapeutic target in FSGS. Key Takeaways:Podocytes are essential for maintaining the integrity and health of the kidney.Podocyte damage directly contributes to proteinuria and disease progression.Proteinuria is both a symptom and a driver of FSGS disease progression.Endothelin 1 and angiotensin II promote podocyte dysfunction. Speakers: Tobias Huber is the Chair of the Center of Internal Medicine at University Medical Center Hamburg-Eppendorf, Germany and president of the International Society of Glomerular Disease.Chris Gisler is a medical director at Travere Therapeutics and a community nephrologist practicing in Pittsburgh.

Title:  Intro to FSGSEpisode Description: In this episode of the Rare Kidney Disease Show, Howard Trachtman, Adjunct Professor of Pediatrics at the University of Michigan, and Chris Gisler, medical director at Travere Therapeutics, explore the complexities of FSGS, covering its pathophysiology, classifications, and clinical presentation. They discuss key drivers of kidney failure, challenges in diagnosis and management, and the unmet need for safe and effective treatments. Listeners will gain insights into the patient journey, role of precision medicine, disease heterogeneity, and the future of clinical trial design. The episode concludes with how PARASOL is shaping advancements in FSGS research and clinical trials. Key Takeaways:Evolving Classification of FSGS – Once defined primarily by histopathology, FSGS is now recognized as a heterogeneous disorder with distinct genetic, immune, and metabolic etiologies. This shift has critical implications for diagnosis and treatment.FSGS and the Role of Podocyte Injury – Podocyte loss is a key driver of FSGS progression, with genetic, immune, and metabolic insults leading to irreversible damage. Understanding this mechanism is crucial for developing targeted therapies.Challenges in Treatment and Therapeutic Gaps – Current treatment strategies rely on empiric use of steroids and calcineurin inhibitors, with variable efficacy and significant side effects. A more targeted approach is needed to improve patient outcomes.Speakers: Howard Trachtman is the Adjunct Professor of Pediatrics at the University of Michigan.Chris Gisler is a medical director at Travere Therapeutics and a former community nephrologist practicing in Pittsburgh.

In this episode of the Rare Kidney Disease Show, a panel of nephrology experts explore the latest data on sparsentan, as presented at ASN Kidney Week 2024.Dr. Hiddo Heerspink presents a post hoc analysis of the PROTECT trial comprised of patients who achieved complete proteinuria remission.Dr. Chee Kay Cheung shares interim data from the SPARTAN study on sparsentan therapy in treatment-naïve patients with IgA nephropathy.Lastly, Dr. Bruce Hendry discusses combination treatment of sparsentan with SGLT2i in the SPARTACUS study. These discussions are introduced by Dr. Edgar Lerma, who offers his insights into the possible clinical implications of these data. 

Luis Velez, MD is a board-certified community nephrologist in San Antonio, TX with expertise in hypertension and glomerular disorders.  Jessica Coleman, MD is a board-certified community nephrologist practicing between Savanah, GA and Charleston, SC with expertise in hypertension and glomerular disorders.  In this episode, Drs Velez and Coleman discuss management of IgAN patients from the viewpoint of community nephrologists. They discuss the evolution in their management of IgAN, highlighting the availability of new data such as RaDaR as a key driver of change. With greater awareness of the role of proteinuria, they advocate for early and aggressive treatment to avoid long term complications of IgAN.  Key Quotes: “RaDaR taught me that the traditional way of looking at IgA nephropathy is wrong. We realized this is a disease state that absolutely can progress and can progress more rapidly than what we initially appreciated and certainly at a younger age in these patients. (02:25) “When we look at patients with proteinuria, even just 0.5 g/d, a third of patients under 40 are going to progress to end stage kidney disease in ten years [RaDaR].” (04:30)“With the RaDaR data, we see levels of proteinuria 0.5 -0.8 g/d still being significant markers for disease progression.” (08:56)Key Takeaways:IgAN is not a benign diseaseProteinuria is the most important prognostic indicator of disease progression in IgA NephropathyHCPs should be targeting lower proteinuria goals to achieve complete remission <0.3 g/dThe updated KDIGO Guidelines should support clinicians’ decisions to target complete remission

Episode Overview: Donald Kohan, PhD is an Emeritus Professor at the University of Utah Health with expertise in endothelin receptors, sodium transporters, and the renin-angiotensin-aldosterone system in chronic kidney disease.In this episode, Professor Kohan provides an overview of the endothelin system and how it relates to the pathophysiology of chronic kidney disease and IgA nephropathy specifically. Key Quotes: “Endothelin 1 is a really unusual molecule. It's highly stable because it has 2 interchain disulfide bonds that resist degradation. It's extremely potent having about 10 fold higher potency than any other known vasoactive factor.”“Angiotensin and ET-1 cause their effects through different pathways.”“Angiotensin stimulates transient calcium release, which causes more short-term contraction and other effects. While endothelin 1 stimulates more sustained calcium release, which then elicits longer lasting pathophysiologic effects.”Key Takeaways:(04:41) Endothelin-1 acts via ETA receptors to cause vasoconstriction, fibrosis, cell proliferation and other effects that promote chronic kidney disease(06:15) The endothelin and renin-angiotensin systems interact, forming a vicious cycle that worsens kidney injury (12:19) In IgA nephropathy models, combined ETA + angiotensin receptor blockade with sparsentan reduced proteinuria and kidney injury more than angiotensin blockade aloneDisclaimer: Guest speakers of the Rare Kidney Disease Show may be paid consultants of Travere Therapeutics. This podcast episode was recorded on May 7, 2024. Please always consult updated sources for the latest information, as information discussed may have changed since the recording date

Overview:In this episode of the Rare Kidney Disease Show, Professor Jonathan Barratt discusses the need to take a long-term approach when managing IgA nephropathy patients. He presents data from the UK National Registry of Rare Kidney Diseases (RaDaR). During this recording you will hear Professor Barratt discussing the continued risk of progression to end stage renal disease even in patients with proteinuria of less than 1g/day, the current threshold of high risk as per KDIGO guidelines. The data from the UK has been reinforced by recent database studies and these will also be discussed by Professor Barratt.Key Quotes: "If you have IgA Nephropathy and you're diagnosed as a child, half of those children have developed kidney failure at 20 years.""We need to be thinking, what is it like for that patient in front of us being 50 or 60, not necessarily what's going to happen in the next five or ten years.""If we don't think the longer term, we're going to under-treat and not serve our patients well." Key Takeaways:IgA nephropathy patients often have decades of life ahead of them, so physicians should focus on minimizing lifetime risk of kidney failure rather than short-term outcomes (00:02:11)RaDaR data shows high rates of kidney failure among IgA nephropathy patients in the UK, even those diagnosed and treated as children (00:04:05)Per the RaDaR publication, an eGFR decline of <1 ml/min per 1.73 m2 per year must be the target if patients are to avoid kidney failure (00:06:48)In the UK, 1 in 4 IgA nephropathy patients with 0.5-1 g/day proteinuria reach ESRD within 10 years (00:08:23)Recent US database searches confirm high rates of CKD progression and kidney failure in IgA nephropathy patients, even those with lower proteinuria levels (00:13:20)Disclaimer: Guest speakers of the Rare Kidney Disease Show may be paid consultants of Travere Therapeutics. This podcast episode was recorded on April 24, 2024. Please always consult updated sources for the latest information, as information discussed may have changed since the recording date.