A Study to Assess the Safety and Tolerability of E8001 in Healthy Male Participants

PHASE1CompletedINTERVENTIONAL
Enrollment

36

Participants

Timeline

Start Date

October 28, 2020

Primary Completion Date

August 18, 2023

Study Completion Date

August 18, 2023

Conditions
Healthy Volunteers
Interventions
DRUG

E8001

Intravenous infusion.

DRUG

Placebo

Intravenous infusion.

Trial Locations (1)

Unknown

Eisai Trial Site #1, Minatoku

All Listed Sponsors
lead

Eisai Co., Ltd.

INDUSTRY

NCT04609852 - A Study to Assess the Safety and Tolerability of E8001 in Healthy Male Participants | Biotech Hunter | Biotech Hunter