292
Participants
Start Date
September 1, 2015
Primary Completion Date
February 1, 2019
Study Completion Date
December 22, 2023
DS-8201a (DP1)
DS-8201a to be administered via intravenous (IV) dose. DS-8201a (DP1) was used for the Dose Escalation phase and for Dose expansion Parts 2a, 2b, 2c, and 2d.
DS-8201a (DP2)
DS-8201a is to be administered via intravenous (IV) dose. DS-8201a (DP2) was used only used for Dose Expansion Part 2e.
DS-8201a (DP)
DS-8201a (DP) is to be administered via intravenous (IV) dose.
Memorial Sloan-Kettering Cancer Center, New York
Mayo Clinic, Jacksonville
University of Louisville, Louisville
UC Health Clinical Trials Office, Cincinnati
Washington University School of Medicine, St Louis
Sharp Memorial Hospital, San Diego
Dana Farber Cancer Institute, Boston
University of Texas M. D. Anderson Cancer Center, Houston
Aichi Cancer Center Hospital, Aichi
National Cancer Center Hospital East, Chiba
Social Medical Corporation Hakuaikai Sagara Hospital, Kagoshima
Kindai University Hospital, Osaka
National Cancer Center Hospital, Tokyo
The Cancer Institute Hospital of Japanese Foundation For Cancer Research, Tokyo
Lead Sponsor
Collaborators (2)
Daiichi Sankyo
INDUSTRY
AstraZeneca
INDUSTRY
Daiichi Sankyo Co., Ltd.
INDUSTRY