drugset / Trial / NCT03386942

A Study of MORAb-202 (Herein Referred to as Farletuzumab Ecteribulin) in Participants With Solid Tumors

NCT03386942

Phase 1 Completed 82 enrolled Eisai Inc.
NaSingle-groupOpen-labelTreatment

Summary

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

Timeline

Start
2017-11-28
Primary completion
2022-10-26
Completion
2022-10-26

Drugs

EvaluationDrugModalityDoseRoute
Subject Farletuzumab Ecteribulin Unknown 0.3 mg/kg Intravenous
Subject Farletuzumab Ecteribulin Unknown 0.9 mg/kg Intravenous
Subject Farletuzumab Ecteribulin Unknown 1.2 mg/kg Intravenous

Indications