跳至主要内容
临床试验/ISRCTN84512041
ISRCTN84512041进行中(未招募)1 期

A single-center, open-label, two-period study to investigate the effect of multiple-dose itraconazole, a strong CYP3A inhibitor, on the pharmacokinetics of a single dose of RO7269162 in healthy participants

F. Hoffmann-La Roche Ltd0 个研究点目标入组 18 人开始时间: 2024年5月17日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
18

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. Body mass index (BMI) of 18 to 30 kilograms per metre squared (kg/m2) inclusive (at screening)
  • 2. Participants who are overtly healthy determined by no clinically significant findings from medical history, 12-lead electrocardiogram (ECG), or vital signs

排除标准

  • 1. History or presence of any clinically significant cardiovascular, bronchopulmonary, hepatic, renal, gastrointestinal, endocrinological, hematological, neurological, psychiatric, genitourinary, metabolic disorders, allergic diseases, cancer, or cirrhosis
  • 2. History or evidence of any medical condition capable of significantly altering the absorption, metabolism, or elimination of drugs
  • 3. Surgical history of the gastrointestinal tract affecting gastric motility or altering the gastrointestinal tract
  • 4. History of malignancy in the past 5 years
  • 5. Known active or uncontrolled bacterial, viral, fungal, mycobacterial infection, or other Infection
  • 6. Participation in an investigational drug study involving any therapeutic monoclonal antibody
  • 7. Positive test for drugs of abuse or alcohol
  • 8. Positive result on human immunodeficiency virus (HIV) 1 and HIV2, hepatitis C virus (HCV) or hepatitis B virus (HBV)
  • 9. Participants who have donated over 500 milliliters (mL) of blood or blood products or had significant blood loss within 3 months before screening.

研究者

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