Advancing Therapies From Discovery to Patients Through Novel Target Evaluation, Validation of Meaningful Surrogate Endpoints, & Optimized Patient Stratification to Be the First to Market in New Indications
As competition intensifies across rare and genetic kidney disease pipelines, companies are under increasing pressure to differentiate assets, generate robust clinical data, and accelerate timelines to market. Across IgAN, FSGS, ADPKD, Alport syndrome, and C3G, accelerated approval pathways have reshaped how teams approach target validation, endpoint selection, and trial design in small and heterogeneous patient populations. With more programs advancing than ever before, teams must make faster, higher-stakes decisions to secure first- and best-in-class positioning.
At the same time, challenges in patient recruitment, uncertainty around surrogate endpoints in the clinic, and gaps in mechanistic disease understanding continue to limit trial success and delay development timelines. As a result, there is a growing need for more precise patient stratification, stronger translational models, and smarter, more efficient approaches to clinical trial design.
The 6th Rare & Genetic Kidney Disease Drug Development Summit brings together leading experts across biopharma, academia, and patient advocacy to address these barriers head-on. Drawing on experience from organizations advancing approved and late-stage therapies, including Novartis, Calliditas, and Travere Therapeutics, this meeting spans discovery through commercialization and provides a focused forum to share real-world data, pressure-test development strategies, and align on what it takes to advance renal disease therapies.
Join the community advancing the next generation of kidney therapies and leave with practical insights you can apply directly to your programs.
Attending Companies Include