drugset / Trial / NCT02564900

Study of DS-8201a in Subjects With Advanced Solid Malignant Tumors

NCT02564900

Phase 1 Completed 292 enrolled Daiichi Sankyo AstraZeneca · collab
Non-randomizedSequentialOpen-labelTreatment

Summary

This is an open-label, two-part, multicenter study to evaluate the safety and tolerability of DS-8201a in participants with advanced solid malignant tumors.

Timeline

Start
2015-09-01
Primary completion
2019-02-01
Completion
2023-12-22

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Trastuzumab deruxtecan Monoclonal antibody 0.8 mg/kg Intravenous
Subject Trastuzumab deruxtecan Monoclonal antibody 1.6 mg/kg Intravenous
Subject Trastuzumab deruxtecan Monoclonal antibody 3.2 mg/kg Intravenous
Subject Trastuzumab deruxtecan Monoclonal antibody 5.4 mg/kg Intravenous
Subject Trastuzumab deruxtecan Monoclonal antibody 6.4 mg/kg Intravenous
Subject Trastuzumab deruxtecan Monoclonal antibody 8 mg/kg Intravenous

Indications