Locally advanced/metastatic urothelial carcinoma
Overall Survival (OS)
Progression-Free Survival (PFS), Objective Response Rate (ORR), Duration of Response (DOR), Number of Participants Who Experience an Adverse Event (AE), Number of Participants Who Discontinue Study Treatment Due to an AE, Change From Baseline in European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire-Core 30 (EORTC QLQ-C30) Global Health Status/Quality of Life (Items 29 and 30) Combined Score, Change From Baseline in EORTC QLQ-C30 Physical Functioning (Items 1-5) Combined Score, Change From Baseline in EORTC QLQ-C30 Role Functioning (Items 6 and 7) Combined Score, Change From Baseline in EORTC QLQ-C30 Fatigue (Items 10, 12, and 18) Combined Score, Change From Baseline in EORTC QLQ-C30 Nausea/Vomiting (Items 14 and 15) Combined Score, Change From Baseline in EORTC QLQ-C30 Diarrhea (Item 17) Score
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.
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