Phase I Single-Dose Safety and Phamacokinetics Clinical Study of Resveratrol AKA IRB 2003-424
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 40
- 试验地点
- 4
研究概览
简要总结
RATIONALE: Chemoprevention is the use of certain drugs to keep cancer from forming, growing, or coming back. The use of resveratrol may prevent cancer.
PURPOSE: This phase I trial is studying the side effects and best dose of resveratrol in preventing cancer in healthy participants.
详细描述
OBJECTIVES:
- Determine the concentration of resveratrol and its metabolites in the plasma, urine, and feces of healthy participants.
- Correlate dose with systemic concentration of this drug and its metabolites in these participants.
- Determine the safety of this drug in these participants.
OUTLINE: This is an open-label, dose-escalation, multicenter study.
Beginning 5 days before study drug administration, participants are put on a controlled diet (avoiding all resveratrol-containing food or drink) for washout. Participants receive oral resveratrol once on day 1.
Cohorts of 10 participants receive escalating doses of resveratrol until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 10 participants experience dose-limiting toxicity. A total of 16 participants are treated at the MTD.
研究设计
- 研究类型
- Interventional
- 主要目的
- Prevention
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 80 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •DISEASE CHARACTERISTICS:
- •Healthy participants
- •PATIENT CHARACTERISTICS:
- •Performance status
- •Life expectancy
- •Not specified
- •Hematopoietic
- •Absolute neutrophil count > 1,500/mm^3
- •Platelet count 120,000-450,000mm^3
- •Hemoglobin 10.5-17.5 g/dL for women OR 11.5-19.0 g/dL for men
- •Bilirubin 0.05-1.2 mg/dL
- •AST and ALT < 1.5 times normal
- •Creatinine normal
- •Urinalysis normal
- •Not pregnant or nursing
- •Negative pregnancy test
- •Fertile participants must use effective contraception
- •Willing to abstain from ingesting large quantities of resveratrol-containing foods
- •Willing to spend 24 hours in the hospital
- •No cancer diagnosis that is currently under treatment, is clinically detectable, or that has been treated within the past 5 years except basal cell or squamous cell skin cancer
- •No concurrent excessive alcohol intake (>21 units per week for men; 14 units per week for women)
- •PRIOR CONCURRENT THERAPY:
- •Biologic therapy
- •Not specified
- •Chemotherapy
- •Not specified
- •Endocrine therapy
- •Concurrent hormone replace ment therapy allowed
- •Concurrent oral or depot contraceptives allowed
- •Radiotherapy
- •Not specified
- •Not specified
- •At least 2 weeks since prior and no concurrent vitamin supplements of any type
- •More than 6 months since prior and no concurrent participation in any other experimental study
- •No other concurrent chronic medications, including over-the-counter medications, herbal/natural preparations, or dietary supplements
- •No other concurrent prescribed medication
排除标准
- 未提供