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Maximum Tolerated Dose, Safety and Pharmacologic Study of TRF in Women With Breast Cancer

Not Applicable
Conditions
Breast Cancer Female
Registration Number
NCT03855423
Lead Sponsor
Nur Aishah Mohd Taib
Brief Summary

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.

Detailed Description

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

Recruitment & Eligibility

Status
UNKNOWN
Sex
Female
Target Recruitment
12
Inclusion Criteria
  • 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
Exclusion Criteria
  • 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

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Physical AssessmentFor 2 to 4 weeks during supplementation

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

Liver Function TestFor 2 to 4 weeks during supplementation

Liver enzymes with units of U/L

Secondary Outcome Measures
NameTimeMethod
Bioavailability of TRFFor 2 to 4 weeks during supplementation

Blood pharmacokinetic parameters

Trial Locations

Locations (1)

University of Malaya Medical Center

🇲🇾

Kuala Lumpur, Malaysia

University of Malaya Medical Center
🇲🇾Kuala Lumpur, Malaysia
Nur Aishah Taib, MBBS
Contact

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