跳至主要内容
临床试验/ISRCTN16073754
ISRCTN16073754进行中(未招募)1 期

?A Phase I, randomized, double-blind, single ascending dose study ?to evaluate the safety and pharmacokinetics of?GDC-5780 in healthy subjects?

Roche (United States)0 个研究点目标入组 56 人开始时间: 2022年2月9日最近更新:

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
56

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? =18.5 and <30 kg/m²
  • 2. Body temperature of 35°C-37.6°C at screening
  • 3. Systolic blood pressure of 90-139 mmHg and diastolic blood pressure of? 45-89 mmHg at screening
  • 4. Agree to abstain from consumption of grapefruit, grapefruit hybrids, oranges, orange hybrids, pomelos, exotic citrus fruits, and all orange and grapefruit-type fruit juices from 48 hours prior to check-in until clinic check-out (i.e., end of residential stay)
  • 5. Agree to abstain from consumption of alcohol from 48 hours prior to clinic?check-in until clinic check-out
  • 6. Agreement to abstain from consumption of caffeine-containing foods and beverages?(e.g., coffee, tea, chocolate, energy drinks, soda) from 48 hours prior to clinic check-in until clinic check-out

排除标准

  • 1. Pregnancy or breastfeeding, or intention of becoming pregnant during the study or within 14 days after the dose of study drug
  • 2. Planned procedure or surgery during the study
  • 3. Clinical laboratory values outside the normal reference range for the test laboratory at screening, Day?-2, or Day?-1. Participants with an estimated glomerular filtration rate <90 mL/min/1.73 m² at screening, Day?-2, or Day?-1, as calculated using the Chronic Kidney Disease Epidemiology Collaboration equation, must be excluded from the study
  • 4. Positive HIV test at screening
  • 5. Positive hepatitis B surface antigen (HBsAg), hepatitis B core antibody (HBcAb), hepatitis B virus (HBV) DNA test at screening, hepatitis C virus (HCV)
  • 6. Urine sample positive for drugs of abuse at screening or Day?-2
  • 7. Treatment with investigational biologic therapy within 90 days?or 5 drug elimination?half-lives (if known), whichever is longer, prior to initiation of study drug
  • 8. Acute illness within 14 days prior to screening
  • 9. Vaccination within 14 days prior to initiation of study drug

研究者

发起方
Roche (United States)

相似试验