🏥 治験ポータル
← 治験一覧に戻る

健康な被験者におけるオルフォルグリプロン(LY3502970)の単回投与と複数回投与を比較する試験

基本情報

NCT ID
NCT06692348
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
86
治験依頼者名
Eli Lilly and Company

概要

The main purpose of this study is to assess and compare a single capsule and multiple capsules of Orforglipron based on the amount that gets into the blood stream and how long it takes the body to get rid of it, when given to healthy participants under fasted and fed conditions. How the body handles and eliminates the study drug after meals and on an empty stomach will be measured. Information about any adverse effects experienced will be collected and the safety and tolerability of Orforglipron will also be evaluated. The study will last approximately 21 weeks, including a screening period.

対象疾患

Healthy

介入

Orforglipron(DRUG)

依頼者(Sponsor)

実施施設 (3)

医療法人平心会 大阪治験病院

Osaka, Osaka, Japan

博多診療所

Fukuoka, Japan

医療法人 住田病院

Sumida-ku, Tokyo, Japan