drugset / Trial / NCT03473743

A Study of Erdafitinib in Participants With Metastatic or Locally Advanced Urothelial Cancer

NCT03473743

Phase 1/2 Active not recruiting 125 enrolled Janssen Research & Development, LLC
RandomizedSequentialOpen-labelTreatment

Summary

The purpose of this study is to: (a) characterize the safety and tolerability of and to identify the recommended Phase 2 dose (RP2D) and schedule for erdafitinib in combination with cetrelimab, and for erdafitinib in combination with cetrelimab and platinum (cisplatin and carboplatin) chemotherapy and; (b) to evaluate the safety and clinical activity of erdafitinib alone and in combination with cetrelimab in cisplatin-ineligible participants with metastatic or locally advanced urothelial cancer (UC) with select fibroblast growth factor receptor (FGFR) gene alterations and no prior systemic therapy for metastatic disease.

Timeline

Start
2018-04-05
Primary completion
2022-09-30
Completion
2026-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Carboplatin Small molecule Intravenous
Subject Cetrelimab Monoclonal antibody 480 mg Intravenous
Subject Cisplatin Other / unclassified Intravenous
Subject Erdafitinib Small molecule 9 mg Oral

Indications