drugset / Trial / NCT02748837

A Study of ERY974 in Patient With Advanced Solid Tumors

NCT02748837

Phase 1 Completed 29 enrolled Chugai Pharmaceutical
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This is the open label, multicenter Phase 1 study which consists of a dose escalation to determine the maximum tolerated dose (MTD) and cohort expansion to obtain a preliminary evaluation of anti-tumor activity. ERY974 is intravenously injected to patients with Glypican 3 positive advanced solid tumors until unacceptable toxicity or disease progression.

Timeline

Start
2016-08
Primary completion
2019-08
Completion
2019-08

Drugs

EvaluationDrugModalityDoseRoute
Subject ERY974 Unknown Intravenous

Indications