2型糖尿病患者における治験薬(PF-07081532)およびリベルサスの効果、ならびに肥満患者におけるPF-07081532の効果を個別に評価する治験
基本情報
- NCT ID
- NCT05579977
- ステータス
- 中止
- 試験のフェーズ
- 第2相
- 試験タイプ
- 介入
- 目標被験者数
- 902
- 治験依頼者名
- Pfizer
概要
The purpose of this study is to find out if PF-07081532 ("the active study drug"), is safe and helps treat people with obesity without diabetes to lose weight, and people with diabetes to keep their blood sugar in good control. Individuals diagnosed with diabetes that are on metformin or individuals with obesity without diabetes will be included in the study. Those participating in the diabetes part of the study, will receive either active study drug, placebo, or an approved treatment called Rybelsus. Those in the obesity part of the study, will receive either active study drug or placebo. The study will last for about 36 weeks except for the first 25% of the participants that enter in which case the study will last for approximately 48 weeks. during this time there will be visits every 4 weeks with phone calls in between.
対象疾患
介入
依頼者(Sponsor)
実施施設 (9)
清和医院
Adachi-ku, Tokyo, Japan
Medical Corporation Heishinkai ToCROM Clinic
Shinjuku-ku, Tokyo, Japan
医療法人平心会 ToCROMクリニック
Suita-shi, Osaka, Japan
医療法人 白岩内科医院
Kashihara, Osaka, Japan
Nakakinen clinic
Naka, Ibaraki, Japan
医療法人社団新東会横浜みのるクリニック
Yokohama, Japan
医療法人社団福和会 福和クリニック
Chuo-ku, Tokyo, Japan
医療法人社団旭和会 東京駅センタービルクリニック
Chuo-ku, Tokyo, Japan
医療法人社団知正会 東京センタークリニック
Chuo-ku, Tokyo, Japan