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

PHASE1CompletedINTERVENTIONAL
Enrollment

82

Participants

Timeline

Start Date

November 28, 2017

Primary Completion Date

October 26, 2022

Study Completion Date

October 26, 2022

Conditions
Solid Tumors
Interventions
DRUG

Farletuzumab Ecteribulin

Part 1: farletuzumab ecteribulin intravenous (IV) infusion administered every 3 weeks starting at a 0.3 mg/kg dose and successively increasing doses until DLT. Part 2: farletuzumab ecteribulin administered IV every 3 weeks at a dose determined in Part 1 until any of the criteria for discontinuation are met.

Trial Locations (10)

Unknown

Eisai Trial Site 5, Matsuyama

Eisai Trial Site 6, Kurume

Eisai Trial Site 8, Sapporo

Eisai Trial Site 4, Akashi

Eisai Trial Site 7, Niigata

Eisai Trial Site 3, Hidaka

Eisai Trial Site 9, Sunto-gun

Eisai Trial Site 1, Chuo-ku

Eisai Trial Site 10, Koto-Ku

Eisai Trial Site 2, Koto-ku

All Listed Sponsors
lead

Eisai Inc.

INDUSTRY

NCT03386942 - A Study of MORAb-202 (Herein Referred to as Farletuzumab Ecteribulin) in Participants With Solid Tumors | Biotech Hunter | Biotech Hunter