EUCTR2021-006534-40-PL进行中(未招募)1 期
Efficacy and safety of oral semaglutide 25 mg once daily in adults with overweight or obesity (OASIS 4) - OASIS 4
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 入组人数
- 300
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1.Informed consent obtained before any study-related activities. Study-related activities are any procedures that are carried out as part of the study, including activities to determine suitability for the study
- •2.Male or female, age greater than or equal to 18 years at the time of signing informed consent.
- •3.Body mass index (BMI) of
- •a)Greater than or equal to 27.0 kg/m^2 with the presence of at least one of the following weight-related complications (treated or untreated): hypertension, dyslipidaemia, obstructive sleep apnoea or cardiovascular (CV) disease
- •b)Greater than or equal to 30.0 kg/m^2.
- •4. History of at least one self-reported unsuccessful dietary effort to lose body weight
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 250
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 50
排除标准
- •1.A self-reported change in body weight greater than 5 kg within 90 days before screening irrespective of medical records
- •2.HbA1c greater than or equal to 6.5% (48 mmol/mol) as measured by the central laboratory at screening
研究者
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