News

Podcast

Kidney Compass: Future of PARASOL and FSGS Management

Key Takeaways

  • Proteinuria reduction is a meaningful measure for drug approval if the drug targets podocyte dysfunction in FSGS.
  • Trial designs should include specimen banking to advance biomarker discovery and refine surrogate endpoints.
SHOW MORE

In the final segment of this episode, the discussion focuses on next steps for the PARASOL Initiative and its potential to transform FSGS drug development.

Welcome to Kidney Compass: Navigating Clinical Trials!

Key Timestamps

00:00 - Episode Start

00:30 - Applying PARASOL Data in FSGS

03:38 - Proteinuria as a Therapeutic Endpoint

07:13 - Future of PARASOL Initiative

In the fourth and final installment of our episode on the PARASOL Initiative and focal segmental glomerulosclerosis, special guests Laura Mariani, MD, MS, and Daniel Gale, PhD, MB BChir, discuss the next steps for the project and its potential to revolutionize drug development in FSGS. Hosts Brendon Neuen, MBBS, PhD, and Shikha Wadhwani, MD, MS, ask Mariani and Gale to explore how the initiative's findings provide a critical pathway for validating proteinuria as a surrogate endpoint in trials.

Gale underscores the importance of recognizing that proteinuria reduction—even without full remission—can serve as a meaningful measure for drug approval. However, he stresses that the drug's mechanism must directly address the underlying podocyte dysfunction central to FSGS pathology. He notes this flexibility could accelerate therapeutic development across various etiologies of FSGS, including genetic, immunologic, and injury-related forms.

Mariani reflects on the significant unmet need in FSGS, emphasizing that even modest reductions in proteinuria can delay dialysis or kidney transplantation—life-changing outcomes for patients. She calls for trial designs that include specimen banking to advance biomarker discovery and refine surrogate endpoints, further enhancing the precision and feasibility of future studies.

Looking ahead, the PARASOL Initiative will focus on publishing its groundbreaking findings and addressing outstanding questions about trial design. Both guests highlight the collaborative nature of this project as a model for tackling similar challenges in other rare kidney diseases. Dr. Gale notes that the Parasol community is a powerful asset for nephrology, offering infrastructure and partnerships to drive research forward in other conditions with limited treatment options.

Kidney Compass: The PARASOL Initiative

Part 1: Introductions

Part 2: PARASOL Background and FSGS Landscape

Part 3: PARASOL Findings and Implications for FSGS

Part 4: Future of PARASOL, FSGS Management (Current Segment)

Relevant disclosures for Neuen include AstraZeneca, Bayer, Boehringer and Ingelheim, Janssen, and others. Relevant disclosures for Wadhwani include the National Institute of Diabetes and Digestive and Kidney Diseases, GSK, Calliditas and Travere Therapeutics. Relevant disclosures for Mariani include Travere Therapeutics, Boehringer Ingelheim, Reliant Glycosciences, Takeda Pharmaceuticals, HI-Bio, and Calliditas Therapeutics. Relevant disclosures for Gale include Novartis, Alexion, Calliditas, Britannia, Vifor, Judo Bio, Adnovate, Sanofi, Anlylam, Boehringer Ingelheim, and Bayer.

Related Videos
Caroline Piatek, MD: High HCRU, Patient Concerns Highlight Great Unmet Need in wAIHA
4 experts are featured in this series.
Steven W. Pipe, MD: Supporting Gene Therapy Implementation for Hemophilia
Corinna L. Schultz, MD: Improving Sickle Cell Trait Documentation in Infancy
Skin of Color Savvy: The Art and Science of Treating Patients of Color
3 experts are featured in this series.
Sibgha Zaheer, MD: Determining Washout Period With Fitusiran, Emicizumab Transition for Hemophilia
© 2025 MJH Life Sciences

All rights reserved.