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Clinical Trials/NCT00976365
NCT00976365
Completed
Phase 2

Phase IIa Study of Metastatic Breast Cancer

Taiwan THL Co.LTd.1 site in 1 country60 target enrollmentOctober 2009

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Metastatic Breast Cancer
Sponsor
Taiwan THL Co.LTd.
Enrollment
60
Locations
1
Primary Endpoint
QOL
Status
Completed
Last Updated
14 years ago

Overview

Brief Summary

The purpose of this study is to obtain evidence from test article with efficacy in Metastatic Breast Cancer patients. The average of all changes from baseline to post-treatment evaluations in global health/quality of life (QoL) subscale assessed by self-administered European Organization for Research and Treatment of Cancer Quality of Life Questionnaire - Core 30 (EORTC-QLQ-C30).

Detailed Description

The test article is extracted from many natural herbals, in which most or their components have been shown to have anti-tumor activity. A study in 2004 showed the test article could have strong immunomodulatory effect on the antigen-stimulated proliferation response (PR) of peripheral blood mononuclear cells (PBMC) and T-cells from recurrent aphthous ulcerations (RAU) patients and suggested that it might be a potential immunoceutical agent for treatment of RAU. Subsequent study in 2005 also suggested the test article as a potential immunoceutical agent for treatment of RAU because the result showed it could modulate the antigen-stimulated cytokine production by T-cells isolated from RAU patients. Another study in 2005 showed the test article also had a broad-range tumor killing function and provided a molecular basis underlying therapeutic activity. It was also suggested in this study will could be a potential and promising cancer therapeutic or preventive agent. The aim of this current study is to explore the safety and efficacy of the investigational product with 20 ml, 3 times per day (daily dose: 60 ml) for a total of 24 weeks in the patients with metastatic breast cancer refractory to conventional treatment modalities.

Registry
clinicaltrials.gov
Start Date
October 2009
End Date
June 2011
Last Updated
14 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • Confirmed breast cancer with clinical evidence.
  • Life expectancy of at least 4 weeks.

Exclusion Criteria

  • Any Uncontrolled infection.
  • Lupus erythematosus.
  • Malignant tumor.

Outcomes

Primary Outcomes

QOL

Time Frame: 6 months measure

Secondary Outcomes

  • CBC with platelet and differential counts. AST, ALT, total bilirubin, BUN, uric acid and Creatinine(6 months measure)

Study Sites (1)

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