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临床试验/NCT02471859
NCT02471859已完成1 期

A Phase 1, Randomized, Double-Blind, Placebo-Controlled, Ascending, Single- and Multiple-Oral-Dose, Safety, Tolerability, and Pharmacokinetic Study of GDC-3280 in Healthy Subjects

Genentech, Inc.0 个研究点目标入组 8 人开始时间: 2015年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
8
主要终点
Number of participants experiencing an adverse event

研究概览

简要总结

This is a Phase 1, Randomized, Double-Blind, Placebo-Controlled, Ascending, Single- and Multiple-Oral Dose, Safety, Tolerability, and Pharmacokinetic Study of GDC-3280 in Healthy Subjects.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Is male or female, using highly effective contraception
  • Has a body mass index (BMI) 18.0 to 30.0 kg/m2, inclusive
  • Is in good general health
  • Having signed informed consent, is willing and able to comply with requirements of the study

排除标准

  • Does not satisfy all screening criteria per protocol
  • Is employed by or related to any personnel involved in the trial
  • Has any history or condition that per protocol or in the opinion of the investigator could compromise the participant's safety or analysis of results

研究组 & 干预措施

Part A: GDC-3280

Experimental

Participants in multiple cohorts and treatment periods will receive single doses of GDC-3280 under fed/fasting conditions.

干预措施: GDC-3280 (Drug)

Part A: Placebo

Placebo Comparator

Participants in multiple cohorts and treatment periods will receive single doses of placebo under fed/fasting conditions.

干预措施: Placebo (Drug)

Part B: GCD-3280

Experimental

Participants in different cohorts will receive GDC-3280 in multiple ascending doses under fed/fasting conditions.\n

干预措施: GDC-3280 (Drug)

Part B: Placebo

Placebo Comparator

Participants in different cohorts will receive placebo in multiple ascending doses under fed/fasting conditions.\n

干预措施: Placebo (Drug)

结局指标

主要结局

Number of participants experiencing an adverse event

时间窗: Up to approximately 6 months

次要结局

  • Total serum clearance for GDC-3280(Up to 4 days)
  • Volume of distribution for GDC-3280(Up to 4 days)
  • Maximum concentration (Cmax) for GDC-3280(Up to 4 days)
  • Time to Cmax (Tmax) for GDC-3280(Up to 4 days)
  • Elimination half-life for GDC-3280(Up to 4 days)
  • Serum GDC-3280 concentration-time data by dosing group(Up to 4 days)

研究者

申办方类型
Industry
责任方
Sponsor

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