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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)
日本イーライリリー株式会社(INDUSTRY)
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