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临床试验/NCT04581772
NCT04581772已完成1 期

A Phase 1 Open-Label, Randomized, Crossover Study to Evaluate the Bioavailability, Effect of Food, Palatability, and Safety of Various DNL343 Oral Formulations in Healthy Participants

Denali Therapeutics Inc.1 个研究点 分布在 1 个国家目标入组 31 人开始时间: 2020年12月23日最近更新:
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
31
试验地点
1
主要终点
PK parameter: Maximum observed concentration (Cmax) of DNL343 in plasma

研究概览

简要总结

This is a Phase 1 relative bioavailability study carried out in approximately 24 healthy male subjects and healthy female subjects of non childbearing potential to investigate the effects of formulation and food on the safety, tolerability, and pharmacokinetics (PK) of DNL343.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Body mass index (BMI) ≥18.5 to < 30 kg/m2 and body weight of at least 50 kg
  • For women: Must have been surgically sterilized or be postmenopausal.

排除标准

  • History of clinically significant endocrine, pulmonary, cardiovascular, gastrointestinal, hepatic, pancreatic, renal, metabolic, hematologic, immunologic, or allergic disease, or other major disorders
  • History of malignancy, except fully resected basal cell carcinoma
  • History of clinically significant neurologic or psychiatric diseases; head trauma with loss of consciousness; or clinically significant depression or suicidal ideation

研究组 & 干预措施

Cohort A

Experimental

干预措施: DNL343 (Drug)

Cohort A

Experimental

干预措施: Placebo (Drug)

Cohort B

Experimental

干预措施: DNL343 (Drug)

Cohort B

Experimental

干预措施: Placebo (Drug)

Cohort C

Experimental

干预措施: DNL343 (Drug)

结局指标

主要结局

PK parameter: Maximum observed concentration (Cmax) of DNL343 in plasma

时间窗: Up to 15 days

PK parameter: Time to maximum observed concentration (Tmax) of DNL343 in plasma

时间窗: Up to 15 days

PK Parameter: Area under the concentration-time curve from time zero to the last quantifiable time point (AUC0-t) of DNL343 in plasma

时间窗: Up to 15 days

PK parameter: The area under the concentration-time curve from time zero extrapolated to infinity (AUC0-∞) of DNL343 in plasma

时间窗: Up to 15 days

次要结局

  • PK parameter: Maximum observed concentration (Cmax) of DNL343 in plasma in the fed versus fasted states(Up to 15 days)
  • PK parameter: Time to maximum observed concentration (Tmax) of DNL343 in plasma in the fed versus fasted states(Up to 15 days)
  • PK Parameter: Area under the concentration-time curve from time zero to the last quantifiable time point (AUC0-t) of DNL343 in plasma in the fed versus fasted states(Up to 15 days)
  • PK parameter: The area under the concentration-time curve from time zero extrapolated to infinity (AUC0-∞) of DNL343 in plasma in the fed versus fasted states(Up to 15 days)
  • Incidence of treatment-emergent adverse events (TEAEs)(Up to 15 days)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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