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健康な日本人男性を対象としたE6007の単回/複数回投与試験

基本情報

NCT ID
NCT02268838
ステータス
完了
試験のフェーズ
第1相
試験タイプ
介入
目標被験者数
24
治験依頼者名
Eisai Inc.

概要

This is a single-center, placebo-controlled, randomized, ascending dose, double-blind study. This study will be evaluating ascending doses of 50, 100, 200, and 400 mg of E6007. This study consists of 5 steps, 1 to 5. In steps 1 to 4 (at ascending doses of 50, 100, 200, and 400 mg), subjects will be randomly assigned in a 6:2 ratio (E6007: placebo) to receive single dose of the study drug under fasted condition. Following 3 days of washout period, subject will receive the study drug once daily for 7 days starting on the fifth day from the single dose administration. For step 3 (200 mg), subjects will subsequently have at least 17 days of washout period before being escalated to step 5 (200 mg) to receive single dose of E6007 under fed condition, to evaluate food effect of the study drug.

対象疾患

Healthy Volunteers

介入

E6007(DRUG)
E6007 matching placebo(DRUG)

依頼者(Sponsor)