PODOMOUNT-Basket, a Phase II, multicentre, randomised, 2-arm parallel-group, double-blind, placebo-controlled basket trial to assess safety, tolerability, PK, and efficacy of BI 764198 in four proteinuric kidney diseases
Condition studied
Proteinuric kidney diseases
Investigational medicinal product(s)
Eligibility
Primary endpoint
Relative change from baseline to Week 20 in 24-hr UPCR (mg/g)
Endpoint detail
Treatment response, defined as at least 25% relative reduction in 24-hr UPCR from baseline to Week 20, Treatment response, defined as at least 40% relative reduction in 24-hr UPCR from baseline to Week 20, Absolute change in eGFR in mL/min/1.73m2 (based on cystatin C) from baseline to Week 20
This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View 2025-523425-17-00 on CTIS ↗ ← All trials in the EU