Xtalks — The Life Science Community™, Online webinar
2026-11-16
Executing clinical trials in complex glomerular diseases require moving beyond traditional functional involvement. As treatment paradigms and regulatory expectations for surrogate endpoints evolve, integrating medical oversight, Advanced Clinical Practitioners (ACPs) and Clinical Operations (ClinOps) from early startup through study closeout is critical to trial success. This webinar explores how an integrated, cross-functional approach can support glomerular disease clinical trials from protocol design through study execution. This webinar presents a practical cross-functional blueprint that bridges early sponsor engagement and protocol design with seamless execution at the site level, while maintaining optimized trial management and regulatory compliance. The featured speakers will explore how embedding nephrology-experienced ACPs alongside therapeutically aligned Medical Monitors and CTMs can help reduce protocol deviations, safeguard primary endpoints and accelerate trial delivery for transformative renal therapies. Additionally, the discussion will examine how sponsors can leverage transferable experience across glomerular disease indications even when disease-specific precedent is limited, applying integrated clinical expertise to evolving endpoint considerations and complex trial procedures. Register for this webinar to learn how cross-functional clinical expertise can strengthen the design and execution of glomerular disease clinical trials.
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Invited Speakers:
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Ajay Srivastava, MD, FASN, Vice President, Medical Department, Medpace Sudha Alphonse, MSc, RN, Advanced Clinical Practitioner, Medpace Sara Rhoten, MSN, RN, Advanced Clinical Practitioner, Medpace Emily Berens, CCRC, Associate Director, Clinical Trial Management, Medpace
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