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Evaluation of the Efficacy of Biobran (Rice Bran Arabinoxylan) in Supporting Breast Cancer Chemotherapy

C

China Medical University

Status

Enrolling

Conditions

Breast Cancer Stages I
Breast Cancer Stages II
Breast Cancer Stage III

Treatments

Dietary Supplement: Biobran supplementation

Study type

Interventional

Funder types

Other

Identifiers

NCT07503496
/CMUH113-REC2-202

Details and patient eligibility

About

This study aims to evaluate the potential supportive effects of rice bran arabinoxylan compound (Biobran) in patients with breast cancer receiving paclitaxel and doxorubicin chemotherapy. The study will assess chemotherapy-related side effects, quality of life, tumor size, tumor antigens, and routine blood test parameters over 24 weeks of treatment.

Full description

Breast cancer is one of the leading causes of cancer-related death among women in Taiwan. Chemotherapy is commonly used in breast cancer treatment, but its associated toxicities, including nausea, vomiting, alopecia, fatigue, tissue toxicity, and immunosuppression, may negatively affect treatment tolerance and quality of life. Biobran is a rice bran arabinoxylan compound that has been reported to possess immunomodulatory, antioxidant, anti-inflammatory, and anti-tumor properties, and may help reduce chemotherapy- and radiotherapy-related side effects. However, evidence regarding its supportive role during breast cancer chemotherapy remains limited. In this study, 96 patients with breast cancer will be recruited from China Medical University Hospital. Participants will receive 3 grams of Biobran daily during 24 weeks. Outcomes will include chemotherapy-related side effects, quality of life, tumor size, tumor antigens, and routine blood test results.

Enrollment

96 estimated patients

Sex

Female

Ages

20 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Breast cancer stage I-III

Exclusion criteria

  • pregnant, lactation, breast recurrence, mental disease, autoimmune disease over hte past 5 years, people who take plant or fungal polysaccharide health supplements

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

96 participants in 2 patient groups

Placebo
No Intervention group
Description:
3 g placebo per day for 24 weeks
Biobran
Experimental group
Description:
3 g Biobran per day for 24 weeks
Treatment:
Dietary Supplement: Biobran supplementation

Trial contacts and locations

2

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Central trial contact

Yi-Chen Huang, PhD; Chong-Kuei Lii, PhD

Data sourced from clinicaltrials.gov

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