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临床试验/NCT03855423
NCT03855423Unknown不适用

Malaysian Tocotrienol Rich Fraction: Immunomodulatory Effect in Women With Breast Cancer

Nur Aishah Mohd Taib1 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2019年2月18日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
12
试验地点
1
主要终点
Physical Assessment

研究概览

简要总结

Phase Ib: Maximum Tolerated Dose, Safety and Pharmacologic Study of TRF in Women with Breast Cancer is aimed to determine the highest, safest and tolerable dose of Tocotrienol-rich Fraction (maximal tolerated dose: MTD) that can be used in women with breast cancer.

详细描述

3+3 step up design method will be used in this study.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

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

入选标准

  • Patients with operable breast cancer
  • Life expectancy of at least 3 months
  • Adequate organ function
  • No allergy to Vitamin E and TRF
  • Provides consent to participate in trial and adhere to the study protocol

排除标准

  • Receiving concomitant chemotherapy, radiotherapy, hormonal, immune therapy or other investigational drugs
  • Uncontrolled concurrent illness
  • Pregnant / breast feeding women
  • Patients who are unable or unwilling to take Tocotrienols, herbal remedies, or non-prescription medications

结局指标

主要结局

Physical Assessment

时间窗: For 2 to 4 weeks during supplementation

Number of participants with treatment-related adverse events as assessed by CTCAE version 5.0

Liver Function Test

时间窗: For 2 to 4 weeks during supplementation

Liver enzymes with units of U/L

次要结局

  • Bioavailability of TRF(For 2 to 4 weeks during supplementation)

研究者

发起方
Nur Aishah Mohd Taib
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Nur Aishah Mohd Taib

Professor

University of Malaya

研究点 (1)

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