drugset / Trial / NCT03444701

A Study of E7130 in Participants With Solid Tumors

NCT03444701 ↗

Phase 1 Completed 62 enrolled Eisai Inc.
Non-randomizedSequentialOpen-labelTreatment

Summary

The primary objective of this study is to evaluate the tolerability and safety profile of E7130 in participants with solid tumors.

Timeline

Start
2018-02-05
Primary completion
2024-12-27
Completion
2024-12-27

Drugs

EvaluationDrugModalityDoseRoute
Subject E7130 Small molecule 25 ug/m2 Intravenous
Subject E7130 Small molecule 270 ug/m2 Intravenous
Subject E7130 Small molecule 300 ug/m2 Intravenous
Subject E7130 Small molecule 350 ug/m2 Intravenous
Subject E7130 Small molecule 400 ug/m2 Intravenous
Subject E7130 Small molecule 410 ug/m2 Intravenous
Subject E7130 Small molecule 480 ug/m2 Intravenous
Subject E7130 Small molecule 550 ug/m2 Intravenous

Indications