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临床试验/EUCTR2021-006534-40-PL
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

ovo Nordisk A/S0 个研究点目标入组 300 人开始时间: 2022年8月12日最近更新:
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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