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Clinical Trials in the EU / 2024-520014-22-00
Completed Phase III

A Phase 3, Randomized, Open-label Study of Sacituzumab Tirumotecan (MK-2870) Versus Investigator’s Choice of Non-platinum Chemotherapy in Participants with Pretreated Locally Advanced/Metastatic Urothelial Carcinoma

2024-520014-22-00 · tracked via the Priya Life Science EU tracker
Sponsor
Merck Sharp & Dohme LLC
Sponsor type
Pharmaceutical company
Therapeutic area
Neoplasms
Decision date
20/04/2026
Enrollment target
265
Sites
Netherlands, Greece, Italy, Germany, Spain, Belgium, Sweden, France

Condition studied

Locally advanced/metastatic urothelial carcinoma

Investigational medicinal product(s)

DOCETAXELMK-2870VINFLUNINEPACLITAXELMK-2870--

Eligibility

Age group
65+ years, 18-64 years
Sex
Female, Male

Primary endpoint

Overall Survival (OS)

Endpoint detail

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

Official registry record

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 2024-520014-22-00 on CTIS ↗ ← All trials in the EU