drugset / Trial / NCT03070990

A Study of Enfortumab Vedotin in Japanese Subjects With Locally Advanced or Metastatic Urothelial Carcinoma

NCT03070990

Phase 1 Completed 19 enrolled Astellas Pharma Inc Seagen Inc. · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

The objective of this study is to assess the safety, tolerability and pharmacokinetics of enfortumab vedotin (ASG-22CE) when administered intravenously to Japanese subjects with locally advanced or metastatic urothelial carcinoma. This study will also assess the immunogenicity as defined by the incidence of anti-drug antibody (ADA) and anti-tumor activity of enfortumab vedotin (ASG-22CE) when administered intravenously to Japanese subjects with locally advanced or metastatic urothelial carcinoma.

Timeline

Start
2017-04-24
Primary completion
2019-02-25
Completion
2019-02-25

Drugs

EvaluationDrugModalityDoseRoute
Subject Enfortumab Vedotin Other / unclassified 1 mg/kg Intravenous
Subject Enfortumab Vedotin Other / unclassified 1.25 mg/kg Intravenous

Indications