固形がん患者を対象としたE7386と他の抗がん剤の併用試験
基本情報
- NCT ID
- NCT04008797
- ステータス
- 募集中
- 試験のフェーズ
- 第1/第2相
- 試験タイプ
- 介入
- 目標被験者数
- 301
- 治験依頼者名
- Eisai Inc.
概要
The primary objective of this study is to assess the safety and tolerability and to determine the recommended Phase 2 dose (RP2D) of E7386 in combination with other anticancer drug(s), and to determine the optimal dose of E7386 in combination with lenvatinib in endometrial carcinoma (EC) (for EC Dose Optimization Part only).
対象疾患
介入
依頼者(Sponsor)
実施施設 (15)
Eisai#1011
Toyoake, Aichi-ken, Japan(RECRUITING)
Eisai#1008
Matsuyama, Ehime, Japan(COMPLETED)
Eisai#1007
Kurume, Fukuoka, Japan(RECRUITING)
Eisai#1009
Hidaka, Saitama, Japan(RECRUITING)
Eisai#1004
Chiba, Japan(COMPLETED)
Eisai#1006
Koto-ku, Tokyo, Japan(RECRUITING)
Eisai#1005
Nagoya, Aichi-ken, Japan(RECRUITING)
Eisai#1002
Kashiwa, Chiba, Japan(RECRUITING)
Eisai#1012
Kamigyō-ku, Kyoto, Japan(COMPLETED)
Eisai#1014
Niigata, Japan(RECRUITING)
Eisai#1010
Kawasaki, Kanagawa, Japan(ACTIVE_NOT_RECRUITING)
Eisai#1001
Chuo-ku, Tokyo, Japan(RECRUITING)
Eisai#1015
Minato-ku, Tokyo, Japan(RECRUITING)
Eisai#1003
Sayama, Osaka, Japan(COMPLETED)
Eisai#1013
Akashi, Hyōgo, Japan(RECRUITING)